- Methodology article
- Open Access

# Detecting groups of coevolving positions in a molecule: a clustering approach

- Julien Dutheil
^{1}Email author and - Nicolas Galtier
^{1}

**7**:242

https://doi.org/10.1186/1471-2148-7-242

© Dutheil and Galtier; licensee BioMed Central Ltd. 2007

**Received:**24 August 2007**Accepted:**30 November 2007**Published:**30 November 2007

## Abstract

### Background

Although the patterns of co-substitutions in RNA is now well characterized, detection of coevolving positions in proteins remains a difficult task. It has been recognized that the signal is typically weak, due to the fact that (i) amino-acid are characterized by various biochemical properties, so that distinct amino acids changes are not functionally equivalent, and (ii) a given mutation can be compensated by more than one mutation, at more than one position.

### Results

We present a new method based on phylogenetic substitution mapping. The two above-mentioned problems are addressed by (i) the introduction of a weighted mapping, which accounts for the biochemical effects (volume, polarity, charge) of amino-acid changes, (ii) the use of a clustering approach to detect groups of coevolving sites of virtually any size, and (iii) the distinction between biochemical compensation and other coevolutionary mechanisms. We apply this methodology to a previously studied data set of bacterial ribosomal RNA, and to three protein data sets (myoglobin of vertebrates, S-locus Receptor Kinase and Methionine Amino-Peptidase).

### Conclusion

We succeed in detecting groups of sites which significantly depart the null hypothesis of independence. Group sizes range from pairs to groups of size ≃ 10, depending on the substitution weights used. The structural and functional relevance of these groups of sites are assessed, and the various evolutionary processes potentially generating correlated substitution patterns are discussed.

## Keywords

- Cluster Approach
- Candidate Group
- Substitution Mapping
- Bottom Node
- Coevolution Analysis

## Background

Measuring the non-independence (= coevolution) of positions (= sites) within a molecule – particularly a protein – is a major challenge of molecular evolution, as witnesses the large methodological effort achieved during the last decade (reviewed in [1]). Several theoretical and experimental arguments link the non-independence of sites to structural and/or functional constraints in proteins. The mechanism most often invoked is the occurrence of compensating mutations, either locally or distantly. Local coevolution may reflect direct residue-residue interaction, whereas distal coevolution is supposed to be the result of more complex mechanisms like secondary structure shifts [2]. But coevolution may also be defined in a broader sense, as correlated evolution: two sites are said to be non-independent if they tend to undergo substitution events in the same branches of the tree. Such events are called co-substitutions [3].

The main pitfall in coevolution detection (and more generally in comparative analysis of biological data) is to distinguish the functional signal from the phylogenetic noise. The latter is due to the shared history of all sites, represented by the underlying phylogenetic tree. Several methods have been developed to assess the departure from independent evolution [2–12]. They differ by (i) the statistic used to measure non-independence (correlation, mutual information), and especially whether it explicitly accounts for the compensatory nature of mutations or not, (ii) the assessment of the level of statistical significance (analytical, randomization, simulation) and (iii) the way they deal with phylogenetic inertia [1]. Global evidence of non-independent evolution between sites has been reported. It has been shown that amino acids in close proximity (see for instance [7, 12]) or belonging to the same proteic domain [8, 13] tend to evolve in a more correlated way than randomly chosen sites. The specific task of pointing to non-independently evolving sites in a given data set, however, suffers from methodological fuzziness and/or deficient software implementation. This probably explains why coevolution detection methods are not routinely used in pipelines for genomic annotation.

Here we introduce a new methodology to detect coevolving groups of sites within a molecule, based on the evolutionary history of these sites. The process is inferred by probabilistic substitution mapping, as we presented in a previous work [11], and is now extended to the protein case. The mapping procedure provides, for each site, an estimate of the number of substitutions in each branch of the tree. This procedure is extended to account for the biochemical properties of the amino acids, by weighting substitution events according to the physico-chemical distance between amino acids. We then define coevolving sites either as sites showing correlated substitution histories, extending the approach of [3], or by sites exhibiting explicit compensation.

It is likely that in proteins one substitution can be compensated by several other substitutions occurring at different positions. Looking for pairs of coevolving sites, as attempted so far, may therefore underestimate the coevolution signal in proteins. Performing an exhaustive search of groups of arbitrary size, however, is inefficient, and in most cases impossible, due to the high number of possible combinations. Clustering techniques are standard methods designed to cope with this issue. Surprisingly, these methods have never been applied to the detection of coevolution. We present here a hierarchical clustering approach to detect good candidate groups of coevolving sites. A statistical procedure is introduced to evaluate the significance of candidate clusters through parametric bootstrap. Using four example data sets, each with its own specificity, we provide evidence that this methodology is successful in making robust predictions of non-independently evolving positions.

## Results

### Algorithm

Given a sequence alignment and a tree, we first define a statistic measuring coevolution for an arbitrary group of sites. Then we introduce a method aiming at seeking candidate coevolving groups by clustering sites according to the coevolution statistics. Finally, we develop a statistical test to assess the significance of candidate groups.

#### Defining a coevolution statistic

*V*, Figure 1a), and can be computed using an empirical Bayesian approach (see methods and [11]). The site-specific, branch-specific numbers of substitutions depend on the set of ancestral states at inner nodes [3, 11], the length of the branch and the rates of substitution between amino acids (or nucleotides). Since the ancestral states are inferred, we have to account for the uncertainty in the reconstruction, by averaging over all possible pairs of ancestral states. A fast, analytical procedure has been developed to achieve this calculation [11].

Here we introduce a generalization of this procedure called "weighted substitution mapping" (see Methods). It is dedicated to proteins and means weighting the different types of substitutions according to the resulting change in a given biochemical property of interest (Figure 1a). In the following, weighted substitution vectors are noted *V**. Entry *k* of vector ${V}_{i}^{\ast}$ is then the estimated amount of biochemical change (*e.g*. change in volume, charge, polarity) having occurred at site *i* in branch *k*.

*i*,

*j*) of sites is measured by the correlation coefficient of the two substitution vectors (Figure 1b) [11]:

*ρ*will be positive and tend toward one. This measure is generalized to a group of arbitrary size

*s*by defining the amount of coevolution for the group as the minimal pairwise correlation between sites in the group:

*ρ*statistic evaluates the tendency of sites to undergo correlated changes, irrespective of the compensatory nature of these changes. Weighted substitution mapping, however, offers the possibility to track the direction of changes, by giving opposite weight to

*X*→

*Y*and

*Y*→

*X*changes. The resulting signed, weighted vectors (noted $\tilde{V}$ in the following) can be used to test the compensatory nature of changes. The underlying assumption is that a given chemical property of a group of coevolving sites (global volume, charge,

*etc*) would tend to be conserved, whereas the properties of individual sites may change. We hereby define

*C*, the compensation index:

*V*| is the length of vectors, that is the L2-norm:

*C*equals 1. On the other extreme, if the vectors are identical,

*C*equals 0. This measure can be generalized for a group of

*s*sites:

Compensation is high when the normalized length of the sum vector of all substitution vectors in the group (noted Σ in Figure 2, bottom) tends to $\overrightarrow{0}$. The correlation (*ρ*) and compensation (*C*) statistics therefore define two distinct detection methods, to be applied sequentially to a given data set.

*i*by taking the length

*N*

_{ i }of its corresponding substitution vector (resp. ${N}_{i}^{\ast}$ for weighted substitution vectors):

*N** statistics provides a new measure of the site-specific rate of change of a given biochemical property – note that the scale of N* depends on the weighting scheme used. The variability of a group of

*s*sites was then defined as the minimum length of substitution vectors of all sites in the group,

*Nmin*:

which is a conservative measure since slowly evolving positions are the less informative. *Nmin* is a nuisance variable on which the coevolution statistics mechanically depend.

#### A clustering approach to select candidate groups

As the size of the tested groups augments, an exhaustive approach quickly becomes intractable, and heuristics should be developed. To detect groups (and not only pairs) of coevolving sites, we performed a cluster analysis of the substitution vectors. We used a complete linkage hierarchical clustering procedure, with the pairwise correlation and compensation distances defined as 1 - *ρ*_{
ij
}and 1 - *C*_{
ij
}respectively. The clustering procedure starts with the pairwise distance matrix *D*, and perform the following steps:

1. Find the pair (*u*, *v*) in *D* with the lowest distance, and cluster the two corresponding sites.

2. Remove the two selected sites *u* and *v* in the matrix, and add the new pair (*u*, *v*) as a single entry.

Compute all distances between the (*u*, *v*) pair and each remaining group using the formula:

*d*(*w*, (*u*, *v*)) = max(*d*(*w*, *u*), *d*(*w*, *v*))

3. Go back to 1, until the matrix size reaches 1.

The use of the maximum function defines the 'complete linkage'. Each step defines a new cluster, and reduces the matrix size by 1. Every cluster of the resulting bifurcating tree is considered as a candidate coevolving group of sites.

#### Assessing the significance of the amount of coevolution

The significance of the clusters was evaluated by parametric bootstrap. One thousand data sets with the same number of sites as the one of interest were simulated, using the estimated tree and parameters. The substitution vectors were computed and the clustering was performed. For each group in the resulting trees, we stored the size of the group, and the corresponding coevolution statistic (*ρ* or *C*) and *Nmin* values. We hence obtained, for each group size, the joint distribution of *ρ* (respectively *C*) and of *Nmin* under the null hypothesis of independence between sites. We then computed the p-value for a group of sites by conditioning over *Nmin*. For instance, for the coevolution statistic *ρ*:

p-value = Pr(*ρ* > *ρ*_{
obs
}|*Nmin*_{
obs
})

*ρ*

_{ obs }is the measured value for statistic

*ρ*. Since

*Nmin*is a continuous variable, we used a window centered on

*Nmin*

_{ obs }to evaluate the p-values:

where *N*_{2} is the number of simulation points with *Nmin* ∈ [*Nmin*_{
obs
}- *ω*/2, *Nmin*_{
obs
}+ *ω*/2], and *N*_{1} is the number of simulation points in this range with a correlation greater or equal to the observed value. *ω* defines the size of the window. In this work we set it to 20% of the range of *Nmin* values.

One potential problem is the fact that nested clusters are not independent. Assume for instance that a triplet of sites actually coevolve. This should result in a significantly high *ρ* for the triplet itself, but perhaps also for pairs within the triplet, or even for certain *n*-uplets including the triplet, thus falsely duplicating the number of significant groups. To correct for this, the method outputs only one cluster – the one with the lowest p-value – when a series of nested clusters is detected. This is a conservative approach, and an improvement over pairwise methods, which typically tend to output large networks of residues (*i.e*. pair (*a*, *b*), pair (*b*, *c*), pair (*c*, *d*), *etc*, *e.g*. [10]).

#### Controlling the false discovery rate

Since we are performing repeated tests, we need to control for the global discovery rate. The clustering approach makes it impossible to rely on classical techniques, due to the non-independence of the tested groups. Here we assessed the false discovery rate by simulations: we conducted our analysis on several data sets simulated under the null hypothesis of independence. As an approximation, and to save computation time, we used the same simulated data sets as those used for computing the single groups p-values: one simulated data set was tested against the 999 remaining ones, and the p-values of the output clusters were recorded. This procedure was repeated 10 times. Now we pooled all the candidate clusters from the 10 analyses, and sort them by p-value. Then we sought the p-value threshold separating the 1% most significant clusters (those with lowest p-values) from the remaining 99%. This threshold is then applied to the real data set to ensure a 1% false discovery rate – only groups of the real-data analysis with a p-value lower than this threshold are considered significant after correction for multiple tests.

### Case studies

To assess its performance, the method was tested on four data sets, each with distinct properties. We now present the detailed results of these analyses and check the predictions with respect to substitution patterns and known protein structure and annotations.

#### Application to rRNA

We applied the new clustering approach with unweighted substitution mapping to a previously studied bacterial rRNA data set, containing 79 large subunit sequences with 2,312 sites [11]. Two hundred and sixty five clusters with a p-values lower than 1% were detected, containing 256 pairs. Two hundreds and forty nine of these pairs (97%) match already known structural stem pairs [14]. The pairwise approach [11] detected 258 pairs, among which 225 structural pairs (87%). The clustering approach hence has even lower false-positive rate than the pairwise approach. The power increase is probably due to the more elaborated p-value computation procedure. Higher order groups are distributed as this: four triplets, one quadruplets, two 5-uplets, one 6-uplets, and one 10-uplet. These groups may be of biological interest but their study is beyond the scope of this article. A detailed list of detected groups is provided as supplementary material.

#### Application to myoglobin

We applied the clustering approach to a myoglobin data set, which has been already scanned for coevolving pairs in previous works [3, 6]. This data set contains 100 sequences, and 144 sites without gaps. In addition to the unweighted mapping, which ignores the nature of the substitutions, we tested four weighting schemes: volume, polarity and charge difference, and the synthetic Grantham chemical distance, a combination of volume, polarity and atom composition [15]. We ran both the correlation and the compensation tests (see methods).

Correlation analysis results for the myoglobin data set.

PDB | Size | Weight | Stat. |
| p-value | FDR | 3D dist. | 3D p-value |
---|---|---|---|---|---|---|---|---|

THR39, GLY65, LEU76, GLU148 | 4 | Volume | 1 | 26.62 | 0.0044** | yes | 28.21 | 0.1688† |

THR39, GLY65, LEU76 | 3 | Unweighted | 1 | 0.98 | 0.0136* | yes | 23.64 | 0.1409† |

LEU11, ALA94, ILE111, ARG118, GLY150 | 5 | Grantham | 0.87 | 78.46 | 0.0045** | yes | 38.14 | 0.7023† |

LEU11, ALA94, ARG118, GLY150 | 4 | Polarity | 0.96 | 2.55 | 0.0065** | yes | 38.14 | 0.8252† |

LEU11, ALA94, ILE111, MET131, LEU135, LEU149, GLY150 | 7 | Volume | 0.82 | 20.89 | 0.007** | yes | 33.1 | 0.1668† |

GLY5, GLY23, GLU52, GLN91 | 4 | Unweighted | 0.47 | 2.67 | 0.0148* | yes | 37.62 | 0.7952 |

LYS56, TYR103 | 2 | Volume | 0.96 | 84.01 | 0.0189* | yes | 21.25 | 0.3506 |

ARG31, SER117 | 2 | Volume | 0.75 | 137.41 | 0.0241* | yes | 11.89 | 0.023*‡ |

SER58, GLU85 | 2 | Unweighted | 0.72 | 1.9 | 0.0245* | yes | 28.12 | 0.6853 |

ALA15, LYS63, ALA84, GLU85, GLN91 | 5 | Grantham | 0.5 | 133.99 | 0.032* | yes | 27.7 | 0.0819. |

ALA15, LEU61, ALA84 | 3 | Unweighted | 0.53 | 2.27 | 0.0346* | no | 26.43 | 0.2817 |

ASP20, PHE33, LEU69, THR95 | 4 | Volume | 0.97 | 20.99 | 0.0347* | yes | 31.15 | 0.3197† |

PHE33, LEU69 | 2 | Unweighted | 1 | 1 | 0.0347* | no | 16.14 | 0.1309‡ |

GLY121, ASP122 | 2 | Unweighted | 0.6 | 3.55 | 0.0379* | no | 3.63 | 0.001*** |

ASP20, GLY23, ASP60, LYS63, ALA84, GLU85, LYS96 | 7 | Charge | 0.46 | 0.99 | 0.0379* | yes | 29.33 | 0.035*† |

GLU105, GLU136 | 2 | Unweighted | 0.74 | 1.77 | 0.0444* | no | 8.25 | 0.003** |

TRP7, LYS47, LYS62 | 3 | Volume | 0.71 | 87.27 | 0.045* | yes | 35.94 | 0.8052 |

Compensation analysis results for the myoglobin data set.

PDB | Size | Weight | Stat. |
| p-value | FDR | 3D dist. | 3D p-value |
---|---|---|---|---|---|---|---|---|

PHE33, LEU69 | 2 | Volume | 1 | 20.99 | 2e-04*** | yes | 16.14 | 0.1339‡ |

PHE33, LEU69 | 2 | Grantham | 1 | 21.99 | 3e-04*** | yes | 16.14 | 0.1339‡ |

PHE33, LEU69 | 2 | Polarity | 1 | 0.3 | 0.0016** | yes | 16.14 | 0.1339‡ |

LEU11, LYS50, TYR103, ARG118 | 4 | Polarity | 0.83 | 5.63 | 0.0014** | yes | 34.22 | 0.5534 |

ALA94, GLY150 | 2 | Polarity | 0.95 | 2.54 | 0.0027** | yes | 8.78 | 0.006**† |

ALA94, GLY150 | 2 | Grantham | 0.93 | 77.72 | 0.0074** | yes | 8.78 | 0.006**† |

PRO37, ALA130 | 2 | Grantham | 0.96 | 94.93 | 0.0034** | yes | 27.81 | 0.6753 |

ALA94, ILE111 | 2 | Volume | 0.87 | 67.97 | 0.0079** | yes | 21.15 | 0.3866† |

THR39, GLY65 | 2 | Volume | 0.98 | 27.63 | 0.0091** | yes | 14.29 | 0.0699.† |

ARG31, SER117 | 2 | Volume | 0.63 | 137.41 | 0.0093** | yes | 11.89 | 0.023*‡ |

ARG31, SER117 | 2 | Grantham | 0.57 | 201.2 | 0.0253* | yes | 11.89 | 0.023*‡ |

LYS42, ASP60, LYS63, THR70 | 4 | Charge | 0.71 | 1.41 | 0.0112* | yes | 20.31 | 0.008** |

GLN26, LYS63, GLU85, TYR103 | 4 | Grantham | 0.76 | 132.11 | 0.0137* | yes | 22.9 | 0.018* |

ASP20, LYS96 | 2 | Charge | 0.6 | 2.23 | 0.0149* | yes | 29.33 | 0.7353† |

THR95, LYS145, GLU148 | 3 | Polarity | 0.63 | 7.42 | 0.0194* | yes | 11.85 | 0.002** |

LEU11, PHE138, GLY150 | 3 | Volume | 0.68 | 41.27 | 0.0333* | yes | 33.1 | 0.6703 |

LYS78, GLU85, ILE99 | 3 | Volume | 0.68 | 37.79 | 0.0373* | yes | 23.37 | 0.1369 |

VAL21, GLN26, ASP27, VAL66, ALA74, LYS78 | 6 | Charge | 0.72 | 1.41 | 0.0415* | no | 24.79 | 0.006** |

LEU9, GLU52, ALA53 | 3 | Polarity | 0.61 | 7.93 | 0.0415* | yes | 33.3 | 0.6993 |

GLN8, LYS42, LYS50 | 3 | Grantham | 0.65 | 117.23 | 0.0455* | no | 38.66 | 0.9171 |

GLY65, LEU76 | 2 | Polarity | 0.95 | 0.89 | 0.0475* | no | 16.46 | 0.1449† |

*e.g*. sites GLY121 and ASP122, located in a external loop of the molecule, ALA94 and GLY150 which are in the end of two helices (see Figure 2A), and sites ARG31 and SER117). Several sites (among the most significant ones) appeared to be located close to the heme group (LEU76, GLY65, THR39 and PHE33, LEU69, see Figure 3a). Finally, we noticed a tendency for sites in helix ends to coevolve (see Figure 3b), a trend already mentioned by [6] and [9].

#### Application to SRK

*Brassicaceae*[16]. The SRK gene is involved in pollen recognition, and is known to be under balancing selection, which results in trans-specific polymorphism [17]. The SRK protein is a transmembrane protein, with a cytoplasmic domain responsible for the kinase activity, and an ectodomain involved in receptor recognition. The ectodomain is highly polymorphic. It includes three hyper-variable regions (HVR), and several sites reported as undergoing positive selection [18] (see Figure 4). No three dimensional structure is available for this protein. The data set we used contains 53 sequences and 386 ungapped sites from the ectodomain.

*et al*. [18]. They are also detected with the compensation method and a Grantham weighting scheme, with a higher p-value. Site 110 is detected as coevolving with site 116 (also known to be under positive selection) for conserving a global polarity level. Another significant group of interest is the pair (350, 352), detected with the Grantham weighting, for the compensation test. These two sites are also reported to be under positive selection and are located in the second hyper-variable region. Together with the study of Sainudiin

*et al*. [18], these results suggest a role for these sites in ligand recognition.

Correlation analysis results for the SRK data set.

Alignment | Size | Weight | Stat. |
| p-value | FDR |
---|---|---|---|---|---|---|

| 2 | Unweighted | 0.75 | 2.93 | 1e-04*** | yes‡ |

| 2 | Grantham | 0.84 | 242.37 | 0.0033** | yes‡ |

| 2 | Volume | 0.79 | 154.32 | 0.0088** | yes‡ |

| 2 | Polarity | 0.76 | 8.82 | 0.0237* | yes‡ |

134, 186, 356, 383 | 4 | Grantham | 0.47 | 205.81 | 0.0115* | yes |

54, 132, 394, 407, 448 | 5 | Grantham | 1 | 56 | 0.0121* | yes† |

54, 55, 132, 248, 394, 407, 410, 429, 448 | 9 | Polarity | 0.97 | 0.7 | 0.0155* | yes† |

54, 55, 132, 394, 407, 429, 448 | 7 | Unweighted | 0.71 | 1 | 0.0166* | yes† |

130, 279 | 2 | Charge | 0.75 | 2 | 0.0232* | yes‡ |

120, 127 | 2 | Charge | 0.74 | 2 | 0.0251* | yes‡ |

25, 49, 70 | 3 | Polarity | 0.77 | 5.61 | 0.0278* | yes† |

65, 121 | 2 | Unweighted | 0.66 | 2 | 0.0362* | yes |

55, 132, 336, 387, 394, 432 | 6 | Charge | 1 | 1 | 0.0438* | yes† |

265, | 3 | Unweighted | 0.45 | 2.22 | 0.0467* | yes |

Compensation analysis results for the SRK data set.

Alignment | Size | Weight | Statistic | Nmin | p-value | FDR |
---|---|---|---|---|---|---|

125, 449 | 2 | Grantham | 1 | 57.93 | 0.0024 ** | yes |

125, 449 | 2 | Volume | 1 | 29.97 | 0.0028 ** | yes |

125, 449 | 2 | Polarity | 1 | 0.5 | 0.0047 ** | yes |

55, 132 | 2 | Polarity | 0.97 | 4 | 0.0039 ** | yes† |

132, 448 | 2 | Grantham | 0.98 | 107 | 0.0061 ** | yes† |

256, 423 | 2 | Charge | 1 | 1 | 0.0067 ** | yes |

120, 127 | 2 | Charge | 0.65 | 2 | 0.0099 ** | yes‡ |

| 2 | Grantham | 0.54 | 314.34 | 0.0112 * | yes |

130, 279 | 2 | Charge | 0.64 | 2 | 0.0118 * | yes‡ |

55, 336 | 2 | Charge | 1 | 1 | 0.0135 * | yes† |

410, 448 | 2 | Polarity | 0.91 | 3.01 | 0.0152 * | yes† |

25, 49 | 2 | Polarity | 0.83 | 5.61 | 0.0181 * | yes† |

236, 375 | 2 | Volume | 0.89 | 62.99 | 0.0185 * | yes |

23, 118 | 2 | Grantham | 0.84 | 141.51 | 0.0234 * | yes |

23, 118 | 2 | Volume | 0.82 | 74.97 | 0.0288 * | yes |

407, 433 | 2 | Grantham | 0.89 | 98.99 | 0.0256 * | yes |

| 2 | Polarity | 0.54 | 12.87 | 0.0321 * | yes |

394, 397 | 2 | Charge | 0.59 | 2 | 0.0338 * | yes |

42, 49 | 2 | Volume | 0.73 | 104.95 | 0.0359 * | yes |

96, 450 | 2 | Charge | 1 | 1 | 0.0369 * | yes |

231, 347, 356 | 3 | Polarity | 0.61 | 10.05 | 0.0393 * | yes |

| 4 | Volume | 0.71 | 120.73 | 0.0473 * | yes |

| 2 | Grantham | 0.53 | 240.8 | 0.048 * | yes‡ |

95, 278, 394, 433 | 4 | Volume | 0.77 | 28.94 | 0.0495 * | no |

The two tests detected sites that are conserved though all the alignment, except for the Q6L8R2_RAPSA allele. Sites 54, 394, 407, 132 and 448 for instance show a conserved polarity throughout the alignment, excepted for the Q6L8R2_RAPSA allele, which shows polarity change for the five sites. This allele is however very divergent from the other alleles (see Figure 3). It belongs to the so-called class II category, which contains only few alleles that are all recessive to alleles from the class I category [19]. These two categories form two distinct clades separated from each other about 40 millions years ago [20].

#### Application to MAP

*et al*. [10]. The coevolution signal was higher in this data set, probably at least partly because of the higher number of sequences (147), which leads to more powerful tests: a total of 43 groups with p-value < 1% were detected with the correlation test (among which 38 remain significant after correction for multiple testing). Surprisingly, the compensation statistic led to a lower number of detected groups (13, among which 10 remain significant after multiple testing correction). Most of the groups were pairs or triplets of sites in contact or in significantly close proximity (see Figure 3c and 3d). Several sites were also located in or close to the active site. Substitution maps for these groups clearly pointed to a large number of cosubstitution and compensatory events, as illustrated by Figure 6.

*et al*. [10]. They found two kinds of coevolving pairs: one involving sites in close proximity, and a set of interconnected residues belonging to a large cluster. Gloor

*et al*. [10] used mutual information (MI), after correcting for slowly evolving sites. Their statistic, however, does not account for the underlying phylogeny, which may lead to several false positives. In their study, this problem was addressed by considering only the most significant correlated sites, assuming that their correlation is above the background phylogenetic noise. By fully incorporating the phylogeny, we were able to confirm three of their predictions and add several new ones. These confirmed pairs are the three most significant ones according to our correlation method, and appear to be in contact in the three dimensional structure. A large proportion of our new predictions also appear to be close in the tertiary structure (see Tables 5 and 6, and Figure 3c and 3d). We were not able to confirm the most significant pair of Gloor

*et al*. [10], neither pairs involved in the large network they report, with the exception of pair (CYS59, THR99) detected for volume compensation and which is close to the ligand. For some of the detected groups no obvious structural interpretation was found. In some cases, these apparent false positives corresponded to sites having undergone correlated changes of evolutionary rate. Figure 7 shows such an example. The five sites in Figure 7 are reasonably variable in general, but invariable in the top-most clade of the tree – presumably because they are under strong functional constraint in this group. Since changes are concentrated in a subset of the branches, the probability that these sites undergo co-substitutions by chance is higher than estimated using a model in which changes can occur throughout the tree, as in the simulations. This is a newly-reported mechanism by which correlated evolutionary patterns can appear in the absence of biochemical interaction between sites.

Correlation analysis results for the MAP data set.

PDB | Size | Weight | Stat. |
| p-value | FDR | 3D dist. | 3D p-value |
---|---|---|---|---|---|---|---|---|

ARG147, ASP187 | 2 | Unweighted | 0.57 | 4.92 | 0*** | yes | 6.24 | 0.001*** |

ARG147, ASP187 | 2 | Grantham | 0.59 | 517.54 | 0*** | yes | 6.24 | 0.001*** |

ARG147, ASP187 | 2 | Volume | 0.58 | 384.76 | 3e-04*** | yes | 6.24 | 0.001*** |

GLN154, GLU158 | 2 | Unweighted | 0.65 | 4.93 | 0*** | yes | 5.96 | 0.001***‡ |

GLN154, GLU158 | 2 | Charge | 0.67 | 4.1 | 1e-04*** | yes | 5.96 | 0.001***‡ |

GLY122, LEU230 | 2 | Unweighted | 0.6 | 6.42 | 1e-04*** | yes | 7.44 | 0.002**‡ |

GLY122, LEU230 | 2 | Grantham | 0.6 | 590.32 | 1e-04*** | yes | 7.44 | 0.002**‡ |

GLY122, LEU230 | 2 | Polarity | 0.61 | 18.34 | 1e-04*** | yes | 7.44 | 0.002**‡ |

GLY122, LEU230 | 2 | Volume | 0.48 | 275.16 | 0.0052** | yes | 7.44 | 0.002**‡ |

ALA21, LEU25, GLY107 | 3 | Unweighted | 0.45 | 4.09 | 1e-04*** | yes | 12.07 | 0.001*** |

LEU25, GLY107 | 2 | Grantham | 0.52 | 312.81 | 0.0077** | no | 12.07 | 0.031* |

THR241, GLY244 | 2 | Unweighted | 0.57 | 3.24 | 3e-04*** | yes | 5.11 | 0.001*** |

ASN46, SER68 | 2 | Unweighted | 0.48 | 4.67 | 5e-04*** | yes | 5.92 | 0.001*** |

GLY210, THR225 | 2 | Unweighted | 0.56 | 3.25 | 5e-04*** | yes | 8.28 | 0.004** |

ASP219, TRP221, THR222, THR225, ASP227, GLU235, ILE238, THR241, LEU248 | 9 | Grantham | 0.3 | 68.81 | 6e-04*** | yes | 40.12 | 0.2338† |

TRP221, THR222 | 2 | Unweighted | 0.57 | 2.73 | 0.0014** | yes | 3.75 | 0.001***† |

TRP221, THR225, | 3 | Volume | 0.56 | 105.03 | 0.0092** | no | 18.13 | 0.024*† |

ASP227 | ||||||||

LEU125, THR129 | 2 | Unweighted | 0.53 | 3.21 | 6e-04*** | yes | 6.12 | 0.001*** |

ASN208, SER231 | 2 | Unweighted | 0.48 | 4.32 | 7e-04*** | yes | 4.25 | 0.001*** |

TRP221, THR222, ALA232, GLU235, ILE238, VAL239, THR241, ILE247, LEU248 | 9 | Polarity | 0.28 | 2.15 | 0.001*** | yes | 34.73 | 0.025* |

GLU148, GLU190 | 2 | Unweighted | 0.48 | 5.11 | 0.0011** | yes | 11.88 | 0.03* |

GLU148, GLU190 | 2 | Polarity | 0.5 | 13.91 | 0.006** | yes | 11.88 | 0.03* |

GLY210, GLY244, GLU246 | 3 | Grantham | 0.43 | 302.15 | 0.0012** | yes | 33.45 | 0.4945 |

CYS78, ASN95, SER110, GLY150, GLN233 | 5 | Unweighted | 0.24 | 2.48 | 0.0018** | yes | 21.37 | 0.001*** |

CYS169, GLN182 | 2 | Unweighted | 0.45 | 4.39 | 0.0018** | yes | 6.4 | 0.002** |

ILE96, TYR134 | 2 | Unweighted | 0.49 | 5.96 | 0.002** | yes | 18.27 | 0.1768 |

ILE81, PHE113 | 2 | Unweighted | 0.45 | 4.33 | 0.0021** | yes | 16.36 | 0.1259 |

ASP227, ALA232, GLU235 | 3 | Unweighted | 0.48 | 1.41 | 0.0022** | yes | 23.49 | 0.0949. |

ASP219, VAL223 | 2 | Unweighted | 0.46 | 3.66 | 0.0024** | yes | 9.4 | 0.009** |

HIS63, ARG127, GLN130, ALA209 | 4 | Volume | 0.33 | 205.12 | 0.0032** | yes | 32.09 | 0.2527 |

HIS63, GLN130 | 2 | Charge | 0.47 | 5.36 | 0.0035** | yes | 28.75 | 0.5994 |

THR222, SER231, ILE238, VAL239 | 4 | Charge | 0.71 | 0.99 | 0.0039** | yes | 28.93 | 0.1199 |

ARG124, GLU131 | 2 | Grantham | 0.48 | 461.88 | 0.0043** | yes | 10.6 | 0.016* |

GLU131, VAL157, VAL164 | 3 | Unweighted | 0.36 | 4.39 | 0.0045** | yes | 13.43 | 0.001*** |

GLN53, VAL98 | 2 | Grantham | 0.48 | 409.37 | 0.0049** | yes | 13.51 | 0.0579. |

GLU29, VAL32, ILE81, PRO82, THR129, ALA136, ILE149, GLY150, SER163 | 9 | Polarity | 0.21 | 0.1 | 0.005** | yes | 32.31 | 0.008** |

LEU135, PHE156 | 2 | Grantham | 0.49 | 575.88 | 0.0052** | yes | 8.71 | 0.004** |

GLN53, GLU160 | 2 | Charge | 0.44 | 5.85 | 0.0055** | yes | 39.55 | 0.9311 |

VAL56, ILE101 | 2 | Unweighted | 0.51 | 6.53 | 0.0062** | yes | 5.28 | 0.001*** |

VAL56, ILE101 | 2 | Grantham | 0.47 | 457.69 | 0.0069** | no | 5.28 | 0.001*** |

LYS117, GLU123, ARG127 | 3 | Grantham | 0.4 | 487.3 | 0.0076** | no | 15.43 | 0.004** |

PRO118, THR119 | 2 | Polarity | 0.47 | 18.47 | 0.0096** | no | 3.75 | 0.001*** |

ALA232, TYR234, GLU235 | 3 | Charge | 0.87 | 1.41 | 0.0098** | yes | 10.51 | 0.002** |

Compensation analysis results for the MAP data set.

PDB | Size | Weight | Stat. |
| p-value | FDR | 3D dist. | 3D p-value |
---|---|---|---|---|---|---|---|---|

CYS59, THR99, LYS141, SER231 | 4 | Volume | 0.68 | 147.26 | 3e-04*** | yes | 29.66 | 0.1289 |

TRP221, ASP227 | 2 | Grantham | 0.61 | 260.63 | 5e-04*** | yes | 18.13 | 0.1688† |

LEU20, PRO34, ALA55, ASP90, SER132, VAL157, TRP221, ASP227 | 8 | Polarity | 0.75 | 9.96 | 8e-04*** | yes | 38.38 | 0.1548 |

GLY122, LEU230 | 2 | Charge | 0.49 | 3.78 | 9e-04*** | yes | 7.44 | 0.002**‡ |

HIS63, TYR134, GLU180, GLU190, PRO197, ASP242 | 6 | Charge | 0.7 | 3.89 | 0.0016** | yes | 35.58 | 0.1678 |

GLN154, GLU158 | 2 | Charge | 0.48 | 4.09 | 0.0017** | yes | 5.96 | 0.001***‡ |

PHE105, LYS111 | 2 | Volume | 0.47 | 267.57 | 0.0031** | yes | 20.61 | 0.2458 |

VAL24, LYS67, ILE101 | 3 | Volume | 0.58 | 210.55 | 0.0033** | yes | 15.15 | 0.002** |

ASP227, HIS236 | 2 | Charge | 0.49 | 3.15 | 0.0046** | yes | 27.22 | 0.5255 |

THR225, GLY244 | 2 | Grantham | 0.51 | 258.01 | 0.0064** | no | 34.16 | 0.7802 |

VAL157, THR202 | 2 | Grantham | 0.47 | 310.7 | 0.0073** | no | 18.42 | 0.1788 |

ARG19, GLU23, ASN46, VAL50 | 4 | Charge | 0.62 | 5.02 | 0.0086** | yes | 16.04 | 0.001*** |

ALA17, ILE153, TRP221, THR222 | 4 | Volume | 0.66 | 126.09 | 0.0088** | no | 26.58 | 0.0589.† |

It appears that the coevolution signal is weaker in proteins than in rRNA. Fewer groups are detected, with higher p-values and lower correlation statistics. These are groups for which changes occur more frequently in the same branches than expected by chance, but the linkage is not as strong as in rRNA.

### Implementation

The mapping procedure is available as dedicated classes in the Bio++ Phylogenetics library, from version 1.1 [21, 22]. The coevolution detection can be reproduced using the CoMap program, including the pairwise analysis [11] and the clustering analysis (this article). For the clustering analysis, CoMap performs the clustering and the simulation part. As an option, it performs maximum likelihood estimation of model parameters prior to coevolution analysis, and supports a wide range of commonly used model of evolution, from Jukes-Cantor to General Time Reversible for nucleotides, and the Dayhoff and JTT models for proteins, using the dcmutt implementation [23]. CoMap can also read any user-defined model following the PAML format [24]. The p-value computation is done in R, using two scripts distributed along with the program. CoMap is open source and distributed at [25]. The rRNA and protein data sets are also available at this address, together with the results and the scripts used to run the analysis, which may serve as examples for running the coevolution analysis on other data sets. Running time, including the five types of mapping, was between two and five hours for the four data sets analyzed in this study, with a Intel(R) Xeon(TM) 3.06 GHz computer.

## Discussion

In this article we present a new test for detecting coevolving groups of sites based on weighted substitution mapping and a clustering approach. The method is original in (i) detecting groups of arbitrary size, (ii) accounting for the biochemical properties of amino-acid changes, (iii) distinguishing compensatory evolution from other kinds of correlated evolution, (iv) providing the substitution maps corresponding to the detected groups, so that the user can assess the relevance of the detected signal, and (v) being available as a user-friendly program with reasonable running times, easy to integrate into any sequence analysis pipeline.

When applied to a benchmark rRNA data set, the method recovered mostly pairs of sites, as expected, and was more powerful than the approach of [11], although the latter method had been specifically designed to detect pairs. When applied to protein data sets, the method detected candidate groups of coevolving sites of size two to ten. Many of these groups appear relevant from a structural or functional point of view. When applied to the MAP data set, the method detected a higher number of groups than the method of Gloor *et al.*[10], thanks to a more efficient phylogenetic control strategy, and direct assessment of the significance of groups of size higher than two. Coevolving residues were typically located in close proximity, or at the ends of helices, or corresponded to positively selected sites. The method also yielded coevolving groups of sites showing no obvious structural links. We now discuss in more details the various newly-introduced methodological improvements, and the biological mechanisms potentially underlying correlated evolutionary patterns.

### Weighted substitution mapping

A new probabilistic weighted substitution mapping was developed, thanks to the introduction of a weight matrix. A similar approach has been used by [8] and [26], without taking into account ancestral states reconstruction uncertainty. This mapping procedure can have some general interest beyond coevolution detection. It may converge toward the sub-alphabet approach (see for [3] and [18]), by using amino-acid categories (for instance big *versus* small, polar *versus* non-polar, charge *versus* not charges, *etc*) and defining the weight *w*_{x,y}as equal to one if *x* and *y* do not belong to the same category, zero otherwise. Any other amino-acid index or distance may be used, as the ones available in the AAindex database [27]. The mapping is achieved using a fixed topology, assumed to be known. We have previously shown that the coevolution analysis is robust to variations of the underlying tree topology [11].

### Clustering

A usual pitfall when trying to detect coevolving sites without *a priori* knowledge is the high number of putative groups to be tested. An exhaustive approach is possible when only pairs of sites are targeted, but not for groups of arbitrary size: computing 2^{
n
}- *n* - 1 p-values proves to be rapidly unfeasible. One possibility to overcome this issue is to limit the number of groups to test, thanks to the use of multivariate analysis (see [8]) or clustering techniques for instance. Here we used a hierarchical clustering approach, which outputs *n* - 1 clusters of size ≥ 2. A convenient property is that clusters of a same given size are independent and do not overlap. The clustering approach was useful for coevolution detection in drastically reducing the number of groups to be tested.

### Measuring cluster significance

We used two distinct measures of the amount of coevolution for a group. The first one, *ρ*, is the minimum pairwise correlation of sites within the group, and aims at detecting sites with correlated substitutions (co-substitution events). For a pair of sites, the *ρ* statistic is therefore equal to the correlation between the two (weighted) substitution vectors, a measure we introduced in a previous work [11]. The second statistic, *C*, explicitly accounts for the compensatory nature of substitutions. In a previous study, we showed that the coevolution statistic depends on the evolutionary rate of the sites, since slowly evolving sites tend to have artificially high correlation ([11], and also [7, 9, 13]). It is therefore necessary to include a measure of the site variability when assessing the significance of the correlation. We previously used the minimum posterior rate, a measure which is not easily generalizable to the case of weighted vectors. We hence used the length of substitution vectors as a measure of variability in this study. In the case of unweighted vectors, this measure is highly correlated to the posterior rate. To assess the variability of a group of any size, we used the minimum length of the corresponding substitution vector, *Nmin*. This is a summary statistic, since the variability of the group would be fully described only with the complete set of site-specific lengths. The *Nmin* measure is hence an approximation we employed to reduce the number of required simulations. Our approach may easily afford additional summary statistics in order to better account for group variability. We tried using both *Nmin* and *Nmax*. This did not affect the results, but removed some artificially detected groups of large size (> 10, results not shown). The results presented in this paper were obtained by using *Nmin* only and restricting the analysis to groups with a reasonable size, that is, lower than 10.

### Mechanisms of non independent evolution

In this work, coevolution has been defined in a broad sense, *i.e*. as equivalent to non-independent evolution. Sites are considered as coevolving when they tend to undergo (biochemically relevant) substitutions in the same branches of the tree. Co-evolution is hence seen as a non-random distribution of substitutions across the tree and alignment. This non-random distribution, however, may be due to distinct processes. The most intuitive scenario invokes compensatory mutations: one perturbing mutation at a site is compensated by one or several mutations at other sites to maintain a higher order structure. This mechanism corresponds to the definition of coevolution *sensu stricto*, used in most previous works. It relates to (intragenic) epistasis: the selection coefficient of a mutation at one site depends on the states at other sites. Correlated substitution does not necessarily imply compensation, or this compensation may not be seen at the single-molecule level. Sites involved in the recognition of an interacting partner, for instance, may tend to coevolve and be compensated by changes in the interacting molecule. More rarely, sites involved in adaptive process may also undergo correlated changes. Selection toward a new optimum requiring more than one substitution could explain the departure from independence [28]. This scenario should explain the signal detected in the SRK gene, where several coevolving sites have been previously reported to be under positive selection.

Another potential reason for non-independent evolution is a local relaxation of constraint involving several sites, the so-called heterotachy/covarion process [29, 30]. If a structural or functional unit, generally required for proper functioning of the molecule, becomes useless in a specific lineage, then the sites forming this unit will accumulate changes in this lineage. This results in a correlation of rates, which may lead to correlated substitution mappings (see Figure 7). This correlation appears significant if a constant rate among sites is assumed when performing simulations. This may be corrected by using a covarion model as the one proposed by [31]. The two tests we introduce should help distinguishing between correlated states and correlated rates. In agreement with recent work by Hakes *et al*. [32], our analyses suggest that the former mechanism, neglected up to now, could explain a substantial fraction of the detectable correlated patterns.

## Conclusion

The flexible coevolution analysis we propose may provide powerful insight for understanding the evolutionary history of specific genes, similarly to positive selection detection analyses. Another open issue is the importance of coevolutionary processes in protein evolution in general [33]. Systematically applying our approach to a large number of data sets for which structural information is available could help making progress with this respect.

## Methods

The method analyses a set of aligned sequences (*D*) using a phylogeny (assumed to be known), a Markov substitution model and a discrete rate distribution across sites. The set of parameters Θ, including branch lengths, entries in the substitution matrix and rate distribution parameters are estimated using the maximum likelihood (ML) method prior to the co-substitution analysis.

### Substitution mapping

*D*

_{ i }be the

*i*

^{ th }site of the data set,

*i.e*. a column of the alignment. Let

*v*

_{i,b}be the expected number of substitutions that occurred on branch

*b*for site

*i*.

*v*

_{i,b}is computed as follow [11]:

*x*

_{ p }and

*x*

_{ q }are the states at the top and bottom node of the branch for this site. ${n}_{{x}_{p},{x}_{q}}(t)$ is the expected number of substitutions on a branch of length

*t*knowing its initial state

*x*

_{ p }and final state

*x*

_{ q }. We previously showed that the exact computation of this number does not improve the coevolution detection [11], and may be approximated by taking:

where the *c* th rate class has relative rate *r*_{
c
}.

*x*

_{ p }at bottom node, state

*x*

_{ q }at top node, and rate class

*c*given the data and parameters. It can be computed using the formula:

where the first factor of the numerator is the likelihood for site *i* conditional on states *x*_{
p
}and *x*_{
q
}at top and bottom nodes and rate equal to *r*_{
c
}. This likelihood is computed as described by Felsenstein [34], after having multiplied all branch lengths by *r*_{
c
}[35] and summing over all possible ancestral states at each node except for the top and bottom nodes of branch *b*, for which states *x*_{
p
}and *x*_{
q
}are fixed. *P* (*r*_{
c
}) is the prior probability for site *i* of being in rate class *c*, and *P* (*D*_{
i
}|Θ) is the likelihood for site *i*. We call *V*_{
i
}= (*v*_{i,1}, ..., *v*_{i,b}, ..., *v*_{i,m}) (where *m* is the total number of branches in the tree) the *substitution vector* for site *i*.

where *W* = {*w*_{x,y}} is a matrix of substitution weights.

We used the following weights, retrieved from the AAindex database [27]:

• Grantham physico-chemical distance [15], AAindex id: aax2:GRAR740104;

• Difference of volume (as defined by Grantham), AAindex id: aax1:GRAR740103;

• Difference of polarity (as defined by Grantham), AAindex id: aax1:GRAR740102;

• Difference of charge (K and R have +1, D and E have -1, 0 for the others.), AAindex id: aax1:FAUJ880111 and aax1:FAUJ880112;

These weights may be signed or unsigned. By setting *w*_{x,y}= *w*_{y,x}, we aim at detecting sites undergoing simultaneous changes in the given property (*i.e*. correlated evolution). Setting *w*_{x,y}= -*w*_{y,x}accounts for the direction of change, and may hence be used to detect compensatory changes. Signed substitution vectors are noted $\tilde{V}$. The four kinds of vectors were referred as "Grantham", "Volume", "Polarity" and "Charge" in this article. The unweighted vectors (equation 12) were also computed.

### Testing structure proximity

To assess whether sites of a coevolving group were in close proximity in a three dimensional structure, we measured the maximum *C*_{
α
}-to-*C*_{
α
}distance between residues in the group. We constrained the minimal primary distance between sites in randomized groups to be higher than five angstroms, or higher than the minimal primary distance in the tested group, when the latter was lower than five angstroms. We evaluated the significance of the obtained distance by randomization. One thousand groups of the same size were randomly picked from the structure, and their maximum distance measured. The p-value was calculated as the proportion of random groups showing a shorter maximal distance than the tested group.

### Data sets

To compare the clustering approach to the pairwise analysis, we re-analyzed a previously published 79 species bacterial LSU data set [11]. The method was then applied to three protein data sets: the myoglobin of vertebrates, the S-locus Receptor Kinase (SRK) gene of *Brassicaceae*, involved in sporophytic auto-incompatibility, and the Methionine Amino-Peptidase (MAP).

A hundred sequences of myoglobin were retrieved from the Swissprot database and aligned with ClustalX [36]. A phylogenetic tree was built with the PhyML program [37]. The topology was corrected by hand to match well-known branching orders, particularly within mammals [38]. Numerical parameters were then re-estimated while keeping the tree topology fixed.

SRK sequences were retrieved from Swissprot and trEMBL using SRS. Sequences with less than 100 amino acids were removed. A first alignment was performed using the Muscle program [39]. The alignment was visually inspected; ambiguously aligned sequences were removed. The ClustalX program was finally applied to the resulting data set. The final alignment included 53 sequences corresponding to the extra-cellular domain of the protein. A PhyML tree was constructed.

A data set of 174 aligned protein sequences of the Methionine Amino-Peptidase (MAP) was taken from [10]. Their structure-based alignment was used, and a phylogenetic tree was estimated using PhyML. For rRNA data, we used the HKY85 + Γ [40] substitution model, and for protein data the JTT92 + Γ model [41], implemented using the dcmut method [23]. A four-class discretized gamma rate distribution [42] was used in both cases. These models were used for tree building, substitution mapping and parametric bootstrap simulations.

## Availability and requirements

Project name: comap

Project homepage: http://gna.org/projects/comap

Operating systems: Unix, Linux, MacOS and Windows.

Programming languages: C++, R

Other requirements: Bio++ libraries

License: CeCILL Free Software License (GNU GPL compatible, http://www.cecill.info/index.en.html)

## Declarations

### Acknowledgements

The authors would like to thank Aurélie Cailleau and Sylvain Glémin for helping with the SRK analysis, Sylvain Glémin and two anonymous reviewers for helpful comments on this manuscript. This work was supported by Centre National de la Recherche Scientifique and Action Concertée Incitative "Informatique, Mathématiques et Physique pour la Biologie". This publication is the contribution 2007-143 of the Institut des Sciences de l'Évolution de Montpellier (UMR 5554 – CNRS).

## Authors’ Affiliations

## References

- Galtier N, Dutheil J: Gene and protein evolution. 2007, Basel, Karger. Coevolution within and between genes, 3 (chap): 1-12.View ArticleGoogle Scholar
- Neher E: How frequent are correlated changes in families of protein sequences?. Proceedings of the National Academy of Sciences of the United States of America. 1994, 91: 98-102.PubMed CentralView ArticlePubMedGoogle Scholar
- Tuff P, Darlu P: Exploring a phylogenetic approach for the detection of correlated substitutions in proteins. Mol Biol Evol. 2000, 17 (11): 1753-1759.View ArticlePubMedGoogle Scholar
- Göbel U, Sander C, Schneider R, Valencia A: Correlated mutations and residue contacts in proteins. Proteins. 1994, 18: 309-317.View ArticlePubMedGoogle Scholar
- Shindyalov IN, Kolchanov NA, Sander C: Can three-dimensional contacts in protein structures be predicted by analysis of correlated mutations?. Protein Engineering. 1994, 7: 349-358.View ArticlePubMedGoogle Scholar
- Pollock DD, Taylor WR, Goldman N: Coevolving protein residues: maximum likelihood identification and relationship to structure. Journal of Molecular Biology. 1999, 287: 187-198.View ArticlePubMedGoogle Scholar
- Tillier ERM, Lui TWH: Using multiple interdependency to separate functional from phylogenetic correlations in protein alignments. Bioinformatics. 2003, 19: 750-755.View ArticlePubMedGoogle Scholar
- Fleishman SJ, Yifrach O, Ben-Tal N: An evolutionarily conserved network of amino acids mediates gating in voltage-dependent potassium channels. Journal of Molecular Biology. 2004, 340: 307-318.View ArticlePubMedGoogle Scholar
- Dimmic MW, Hubisz MJ, Bustamante CD, Nielsen R: Detecting coevolving amino acid sites using Bayesian mutational mapping. Bioinformatics. 2005, 21 (Suppl 1): i126-i135.View ArticlePubMedGoogle Scholar
- Gloor GB, Martin LC, Wahl LM, Dunn SD: Mutual information in protein multiple sequence alignments reveals two classes of coevolving positions. Biochemistry. 2005, 44: 7156-7165.View ArticlePubMedGoogle Scholar
- Dutheil J, Pupko T, Jean-Marie A, Galtier N: A model-based approach for detecting coevolving positions in a molecule. Mol Biol Evol. 2005, 22 (9): 1919-1928.View ArticlePubMedGoogle Scholar
- Fares MA, Travers SAA: A novel method for detecting intramolecular coevolution: adding a further dimension to selective constraints analyses. Genetics. 2006, 173: 9-23.PubMed CentralView ArticlePubMedGoogle Scholar
- Oliveira L, Paiva ACM, Vriend G: Correlated mutation analyses on very large sequence families. ChemBioChem. 2002, 3: 1010-1017.View ArticlePubMedGoogle Scholar
- Gutell RR, Lee JC, Cannone JJ: The accuracy of ribosomal RNA comparative structure models. Current Opinion in Structural Biology. 2002, 12: 301-310.View ArticlePubMedGoogle Scholar
- Grantham R: Amino acid difference formula to help explain protein evolution. Science. 1974, 185: 862-864.View ArticlePubMedGoogle Scholar
- Takasaki T, Hatakeyama K, Suzuki G, Watanabe M, Isogai A, Hinata K: The S receptor kinase determines self-incompatibility in Brassica stigma. Nature. 2000, 403: 913-916.View ArticlePubMedGoogle Scholar
- Awadalla P, Charlesworth D: Recombination and selection at Brassica self-incompatibility loci. Genetics. 1999, 152: 413-425.PubMed CentralPubMedGoogle Scholar
- Sainudiin R, Wong WSW, Yogeeswaran K, Nasrallah JB, Yang Z, Nielsen R: Detecting site-specific physicochemical selective pressures: applications to the Class I HLA of the human major histocompatibility complex and the SRK of the plant sporophytic self-incompatibility system. Journal of Molecular Evolution. 2005, 60: 315-326.View ArticlePubMedGoogle Scholar
- Nasrallah ME: Developmental regulation of plant gene expression. 1991, Glasgow, UK: Blackie. The molecular basis for sexual incompatibility, 2 (chap): 130-152.Google Scholar
- Uyenoyama MK: A generalized least-squares estimate for the origin of sporophytic self-incompatibility. Genetics. 1995, 139: 975-992.PubMed CentralPubMedGoogle Scholar
- Dutheil J, Gaillard S, Bazin E, Glemin S, Ranwez V, Galtier N, Belkhir K: Bio++: a set of C++ libraries for sequence analysis, phylogenetics, molecular evolution and population genetics. BMC Bioinformatics. 2006, 7: 188-188.PubMed CentralView ArticlePubMedGoogle Scholar
- Bio++: C++ libraries for bioinformatics. [http://kimura.univ-montp2.fr/BioPP]
- Kosiol C, Goldman N: Different versions of the Dayhoff rate matrix. Mol Biol Evol. 2005, 22 (2): 193-199.View ArticlePubMedGoogle Scholar
- Yang Z: PAML 4: phylogenetic analysis by maximum likelihood. Mol Biol Evol. 2007, 24 (8): 1586-1591.View ArticlePubMedGoogle Scholar
- CoMap: a C++ program to detect co-evolving groups of sites. [http://home.gna.org/comap]
- Woolley S, Johnson J, Smith MJ, Crandall KA, Mcclellan DA: TreeSAAP: selection on amino acid properties using phylogenetic trees. Bioinformatics. 2003, 19: 671-672.View ArticlePubMedGoogle Scholar
- Kawashima S, Ogata H, Kanehisa M: AAindex: Amino Acid Index Database. Nucleic Acids Research. 1999, 27: 368-369.PubMed CentralView ArticlePubMedGoogle Scholar
- Orr HA: The population genetics of adaptation: the adaptation of DNA sequences. Evolution. 2002, 56: 1317-1330.View ArticlePubMedGoogle Scholar
- Lopez P, Casane D, Philippe H: Heterotachy, an important process of protein evolution. Mol Biol Evol. 2002, 19 (1): 1-7.View ArticlePubMedGoogle Scholar
- Pupko T, Galtier N: A covarion-based method for detecting molecular adaptation: application to the evolution of primate mitochondrial genomes. Proc Biol Sci. 2002, 269 (1498): 1313-1316.PubMed CentralView ArticlePubMedGoogle Scholar
- Galtier N: Maximum-likelihood phylogenetic analysis under a covarion-like model. Mol Biol Evol. 2001, 18 (5): 866-873.View ArticlePubMedGoogle Scholar
- Hakes L, Lovell SC, Oliver SG, Robertson DL: Specificity in protein interactions and its relationship with sequence diversity and coevolution. Proceedings of the National Academy of Sciences of the United States of America. 2007, 104: 7999-8004.PubMed CentralView ArticlePubMedGoogle Scholar
- Choi SS, Li W, Lahn BT: Robust signals of coevolution of interacting residues in mammalian proteomes identified by phylogeny-aided structural analysis. Nature Genetics. 2005, 37: 1367-1371.View ArticlePubMedGoogle Scholar
- Felsenstein J: Evolutionary trees from DNA sequences: a maximum likelihood approach. Journal of Molecular Evolution. 1981, 17: 368-376.View ArticlePubMedGoogle Scholar
- Yang Z: Maximum-likelihood estimation of phylogeny from DNA sequences when substitution rates differ over sites. Mol Biol Evol. 1993, 10 (6): 1396-1401.PubMedGoogle Scholar
- Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Research. 1997, 25: 4876-4882.PubMed CentralView ArticlePubMedGoogle Scholar
- Guindon S, Gascuel O: A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Systematic Biology. 2003, 52: 696-704.View ArticlePubMedGoogle Scholar
- Murphy WJ, Eizirik E, O'brien SJ, Madsen O, Scally M, Douady CJ, Teeling E, Ryder OA, Stanhope MJ, de Jong WW, Springer MS: Resolution of the early placental mammal radiation using Bayesian phylogenetics. Science. 2001, 294: 2348-2351.View ArticlePubMedGoogle Scholar
- Edgar RC: MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Research. 2004, 32: 1792-1797.PubMed CentralView ArticlePubMedGoogle Scholar
- Hasegawa M, Kishino H, Yano T: Dating of the human-ape splitting by a molecular clock of mitochondrial DNA. Journal of Molecular Evolution. 1985, 22: 160-174.View ArticlePubMedGoogle Scholar
- Jones DT, Taylor WR, Thornton JM: The rapid generation of mutation data matrices from protein sequences. Computer Applications In The Biosciences. 1992, 8: 275-282.PubMedGoogle Scholar
- Yang Z: Maximum likelihood phylogenetic estimation from DNA sequences with variable rates over sites: approximate methods. Journal of Molecular Evolution. 1994, 39: 306-314.View ArticlePubMedGoogle Scholar
- Kraulis PJ: Molscript – a program to produce both detailed and schematic plots of protein structures. Journal Of Applied Crystallography. 1991, 24: 946-950.View ArticleGoogle Scholar
- Merritt EA, Bacon DJ: Raster3d: photorealistic molecular graphics. Methods in Enzymology. 1997, 277: 505-524.View ArticlePubMedGoogle Scholar
- Pupko T, Bell RE, Mayrose I, Glaser F, Ben-Tal N: Rate4Site: an algorithmic tool for the identification of functional regions in proteins by surface mapping of evolutionary determinants within their homologues. Bioinformatics. 2002, 18 (Suppl 1): S71-S77.View ArticlePubMedGoogle Scholar
- Kusaba M, Matsushita M, Okazaki K, Satta Y, Nishio T: Sequence and structural diversity of the S locus genes from different lines with the same self-recognition specificities in Brassica oleracea. Genetics. 2000, 154: 413-420.PubMed CentralPubMedGoogle Scholar

## Copyright

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.