Distinguishing migration from isolation using genes with intragenic recombination: detecting introgression in the Drosophila simulans species complex
- Miguel Navascués^{1, 2},
- Delphine Legrand^{3, 4},
- Cécile Campagne^{4},
- Marie-Louise Cariou^{4} and
- Frantz Depaulis^{1, 5}Email author
https://doi.org/10.1186/1471-2148-14-89
© Navascués et al.; licensee BioMed Central Ltd. 2014
Received: 14 November 2013
Accepted: 3 April 2014
Published: 24 April 2014
Abstract
Background
Determining the presence or absence of gene flow between populations is the target of some statistical methods in population genetics. Until recently, these methods either avoided the use of recombining genes, or treated recombination as a nuisance parameter. However, genes with recombination contribute additional information for the detection of gene flow (i.e. through linkage disequilibrium).
Methods
We present three summary statistics based on the spatial arrangement of fixed differences, and shared and exclusive polymorphisms that are sensitive to the presence and direction of gene flow. Power and false positive rate for tests based on these statistics are studied by simulation.
Results
The application of these tests to populations from the Drosophila simulans species complex yielded results consistent with migration between D. simulans and its two endemic sister species D. mauritiana and D. sechellia, and between populations D. mauritiana on the islands of the Mauritius and Rodrigues.
Conclusions
We demonstrate the sensitivity of the developed statistics to the presence and direction of gene flow, and characterize their power as a function of differentiation level and recombination rate. The properties of these statistics make them especially suitable for analyzing high-throughput sequencing data or for their integration within the approximate Bayesian computation framework.
Keywords
Shared polymorphism Recombination Hybridization Gene flow Incomplete lineage sorting Drosophila simulans complexBackground
Assessing gene flow is essential for any study of speciation or local adaptation, as gene flow is a force counteracting those processes. Classic models of population genetics consider the source of genetic differentiation between populations (F_{ ST }) to result either from an equilibrium between migration and drift (island model) or from drift since the time of divergence (isolation model). Thus, population geneticists would estimate migration rates [1] or time of divergence [2] from F_{ ST } based on their (expert) opinion or other non-genetic evidence that their study system fitted best to one of the two alternative models. The first attempt to distinguish between both scenarios using genetic data was made by Wakeley [3], who noted that the variance of pairwise differences was expected to be higher under the migration model and proposed a test statistic based on this prediction. However, a test based on the variance of pairwise differences shows low power [3], is highly influenced by recombination, and has seen only limited implementation. A significant advance was the development of likelihood-based methods under the isolation-with-migration model e.g. [4]. In this approach, the model consists of two populations that diverge from an ancestral population and exchange migrants, and the values of these parameters (migration rate and divergence time) are inferred. This is currently the most widely used method to study genetic differentiation between a pair of populations or species (see [5] for a review) and is implemented in IMa [6]. The model implemented in IMa assumes the absence of intragenic recombination and the violation of this assumption can produce substantial bias in the estimates from this analysis [7]. A framework to specifically analyse recombining genes is essential as nuclear genes, which are widely used in studies related to divergence and speciation, are subject to recombination. In order to overcome this limitation, likelihood-free methods have also been considered e.g. [8], in which data are summarized by a set of statistics, and the likelihood is approximated by a distance metric between the observed summary statistics and summary statistics simulated from the model. Thus, loci with intragenic recombination can be simulated under the isolation-with-migration model to approximate the likelihood of the parameter values. Similarly, other recent approaches based on summary statistic or the site frequency spectrum e.g. [9, 10], use coalescent simulations with recombination to account for linkage among markers. Recombination generates different linkage disequilibrium patterns depending upon the presence or absence of gene flow ([11]; see next section for details); so genes with recombination potentially provide additional information about genetic exchange. However, because these approximate-likelihood methods reduce the data to a set of summary statistics, information on linkage disequilibrium between polymorphic sites is usually lost (for instance, summary statistics used in MIMAR [8] do not contain this type of information), and any additional information provided by intragenic recombination cannot be exploited. Among the latest related statistical developments, it is worth noting the PAC-likelihood (Product of Approximate Conditional probabilities) method [12] and a method based on shared haplotype lengths [13], both of which explicitly exploit the spatial arrangement of polymorphism within sequences to make inferences under the isolation-with-migration model.
In this work we propose summary statistics that contain information about the presence and direction of gene flow as a result of intragenic recombination, and we describe their properties in the form of statistical tests for the detection of gene flow (note, however, that their use is not necessarily limited to such tests). In order to provide an empirical example, these statistics were calculated in a sample of eleven loci sequenced from populations of the Drosophila simulans species complex (D. simulans, D. sechellia and D. mauritiana, Additional file 1: Figure S4), which is one of the most documented models used for speciation and evolution [14–16]. The generalist D. simulans, which probably evolved on Madagascar [17], has recently extended its distribution globally, is now a semi-domestic species, exhibiting strong genetic differentiation between ancestral and derived populations [18–20]. In contrast, the endemic D. sechellia, confined to the Seychelles archipelago, presents all the characteristics of a island-syndrome species, being strictly specialized on the ripe fruit of the otherwise toxic Morinda citrifolia[21], with low reproductive output [22] and presenting limited genetic diversity [23–25]. Despite its fragmented distribution, D. sechellia does not exhibit strong population structure [25], but rather a local pattern of genetic exchange between neighboring islands [26]. These features strongly contrast with those of its sister species, the island endemic D. mauritiana, which is geographically and genetically highly structured into two populations: the expanding population of Mauritius Island and the population of Rodrigues Island, 600 km to the east of Mauritius, which is smaller and at equilibrium [27]. Interestingly, D. simulans, D. sechellia and D. mauritiana are incompletely reproductively isolated, and can produce fertile female F1 hybrids (males are sterile) [28, 29]. However, the question of interspecific hybridization in nature, and its frequency, is unresolved. The existence of shared polymorphisms between these species may thus result from introgression due to secondary contact, but could also be due to ancestral polymorphism shared among these recently diverged species.
Results and discussion
Spatial arrangement of polymorphism with recombination and gene flow
In order to illustrate the problem at hand, we will consider two extreme models: the isolation (two populations diverging from an ancestral one) and the migration (two populations only connected by gene flow) models. In the case of the isolation model, the origin of S sites are polymorphisms from the ancestral population that have survived drift in both populations since the time of divergence, a process often referred to as incomplete lineage sorting e.g. [31]. In the case of the migration model, shared polymorphism is caused by (possibly recent) exchange of alleles between the populations. It has been argued [11] that S sites had more time to recombine with other sites under the isolation model than under the migration model, and, therefore, stronger linkage disequilibrium (LD) between S sites within each population was expected with the presence of gene flow. However, a preliminary study found that classical measures of LD have little power for the detection of gene flow. While recent gene exchange leaves little time for recombination to act it also leaves little time for (migrant) allele frequencies to increase. Since LD measures are very sensitive to allele frequencies, detecting a significant association between rare migrant alleles is challenging (F. Depaulis, unpublished results). In summary, there are two balanced effects: introgressed alleles may lead to greater LD because they are recent, leaving little time for recombination to occur, however they also tend to be rare, which does not favour high LD values. Note, however, that LD measures might be used to detect admixture [32], i.e. a population originating from the mixture of individuals from different populations, because the targeted pattern is not expected to be overly influenced by low allele frequencies.
Here we argue that gene flow creates some patterns of LD distinct from those created under the isolation model (for an equivalent differentiation level) and which require non-standard measures of LD to reveal them. In the migration model, the fate of a migrant chromosome is to be fragmented by recombination into “introgression blocks”, i.e. segments of DNA of migrant ancestry and untouched by recombination since the migration event (named “migrant tracts” in ref. [33]). Some introgression blocks may be lost by drift, while others may persist. Figure 1 represents a simplified genealogy with migration and recombination (i.e. an ancestral recombination graph; Figure 1A) and a resulting introgression block (Figure 1C, within a grey rectangle). A set of aligned sequences can be divided into segments delimited by the recombination breakpoints (i.e. there would be as many segments as recombination events plus one, represented in Figure 1 with different colours). A segment of the alignment containing an introgression block may contain shared polymorphisms but will rarely contain any fixed difference (except in less likely scenarios, such as when the last lineage with an ancestral state in one population sample migrates to the other population, leaving the source population sample fixed for the mutant allele and the recipient population sample fixed for the ancestral allele). Conversely, a segment of the alignment that does not contain any introgression blocks may contain F sites (lineage sorting is complete) but cannot contain S and F sites together (Figure 1D). Therefore, F and S sites along the alignment are expected to be segregated into a small number of groups.
An alignment can be summarized as a sequence that represents the order of the different categories of polymorphic sites (Figure 1D; ignoring X sites results in a sequence of two elements “FFFFSSFFF” or, in binary coding, “000011000”). We expected the order of elements in this sequence to depart more drastically from randomness in models with migration. The runs test [34] is a statistical test for the randomness in the order of elements of two categories along a sequence. A run is defined as a maximal segment of consecutive elements of the same type (e.g. the sequence “000011000” contains three runs). A low number of runs (R) within a sequence indicates that identical elements appear in clusters along the sequence (e.g. three runs on sequence “000011000” vs. seven runs on sequence “010010010”). Ideally, we would like to apply the test to the sequence of F and S sites, but it is unlikely that both types of sites are present in the same DNA alignment for a large set of parameter values combinations (differentiation level and recombination rate). Therefore, we considered the sequence with the four categories of sites (F, S, X_{1} and X_{2}) and pooled categories of sites, reducing them in two categories. Two combinations were considered: F sites vs. S, X_{1} and X_{2} (e.g. Figure 1D; statistic R_{ F }) and S sites vs. F, X_{1} and X_{2} (e.g. Figure 1D; statistic R_{ S }). Since F and S sites are not often found together, this approach allows testing for either the clustering of F sites (F vs. X) or S sites (S vs. X), whichever are found in the alignment. We predict that values of run statistics (i.e. number of runs, R_{ F } and R_{ S }) will be lower under models with migration than under models of pure divergence.
Spatial arrangement of polymorphism with recombination and unidirectional gene flow
Additional categories of segregating sites can be defined if we consider the distribution of the ancestral and derived alleles between the populations [36]. In practice, the ancestral or derived status of alleles is inferred by the use of an outgroup (Figure 1E). Fixed differences (F) can then be further separated into f_{1} sites, where the derived allele is fixed in P1, and f_{2} sites, where the derived allele is fixed in P2. Among the exclusive polymorphisms of P1 (X_{1}), we can define the category f_{2}x_{1} for cases where the derived state is fixed in P2 (the remaining X_{1} sites will be denoted x_{1} to maintain the nomenclature in [36]; similarly, f_{1}x_{2} and x_{2} sites may be defined. While in [36] all shared polymorphism were considered in the same category, we will distinguish between s_{1} sites for shared polymorphisms with a higher frequency of the derived allele in P1 than in P2, and s_{2} for shared polymorphism with higher frequency of the derived allele in P2.
Consider a stretch of the alignment, delimited by recombination events, unaffected by migration (without any introgression block in any individual) that contains only four types of variable site category: f_{1}, f_{2}, x_{1} and x_{2} (assuming that both populations share a common origin but have been separated long enough for full lineage sorting and for new mutations to have occurred within each population). After a migration event from P2 into P1, an introgression block is introduced into the stretch of alignment considered. Thus, all f_{2} sites become f_{2}x_{1} and all f_{1} sites become x_{1}. Some x_{2} sites may remain x_{2} (migration of the ancestral allele; also, more rarely, some x_{2} may become f_{2} as discussed above) while others may become S sites (migration of the derived allele). Those shared polymorphisms will often belong to category s_{2}, because the mutation is older than the migration event and thus, had more time to increase in frequency in P2 than in P1. Therefore, migration from P2 to P1 will tend to produce clusters of x_{1}, f_{2}x_{1} and s_{2} (Figure 1E), while x_{2} sites will be present along the entire alignment, both within the stretch containing introgression blocks, and outside them. Conversely, migration from P1 to P2 will produce clusters of x_{2}, f_{1}x_{2} and s_{1}, with x_{1} sites distributed along the entire alignment. Lastly, migration in both directions will produce both types of clusters.
As proposed above, an alignment can be summarized as a sequence that represents the order of the different categories of polymorphic sites (Figure 1E). This time, our objective is to independently detect (i) clusters of x_{2}, f_{1}x_{2} and s_{1} sites, and (ii) clusters of x_{1}, f_{2}x_{1} and s_{2} sites within the alignment (as candidates of introgression blocks). In order to test such patterns we will focus on the W statistic [37] which can be used to test for a uniform distribution of the division of a continuous interval into sub-intervals, i.e. the random position (following a uniform probability distribution) of breaks on the continuous interval. The W statistic was modified for the discrete case in ref [38], in order to be able to apply it to molecular sequences. In contrast with the previous R statistic, the modified W statistic is based on the length of the sub-intervals from sites of a given category (0’s) delimited by the positions of the sites of the other category (the ‘breaks’, i.e. the 1’s): $\mathit{W}=0.5{\displaystyle \sum _{\mathit{i}=1}^{\mathit{d}+1}\left|\frac{{\mathit{l}}_{\mathit{i}}}{\left(\mathit{k}-2\right)}-\frac{1}{\mathit{d}+1}\right|}$ where k is the total number of variable sites in the summary sequence, d is the number of sites assigned to category 1 and l_{ i } is the length of the i^{th} sub-interval (there are d + 1 sub-intervals, including those of length zero). Thus, the category 0 is used to define the segment and the W statistic is sensitive to the randomness of the distribution of 1’s. This is an important characteristic of this statistic as it will allow testing for the randomness of one category of site regardless of the other category being distributed randomly or not (so the other category can be tested conversely on exchanging 1’s and 0’s of the sequence). The W statistic will take large values when the ‘breaks’ are clustered and low values when the ‘breaks’ are evenly spaced. This statistic can be applied to our problem by coding the alignment in two ways: (i) x_{1}, f_{2}x_{1} and s_{2} sites as ‘breaks’ (1’s), while x_{2}, f_{1}x_{2} and s_{1} define the segment (0’s) (Figure 1E; statistic W_{x1s2}) and (ii) x_{2}, f_{1}x_{2} and s_{1} sites as ‘breaks’ (1’s), while x_{1}, f_{2}x_{1} and s_{2} define the segment (0’s) (Figure 1E; statistic W_{x2s1}). Preliminary work on a variant of the W statistic including fixed differences yielded similar results (data not shown). It will thus not be presented in this work. We predict that the presence of migration from P2 to P1 (bidirectional migration or unidirectional migration from P2 to P1) will produce larger values in the statistic W_{x1s2} than scenarios without migration from P2 to P1 (isolation model and unidirectional migration from P1 to P2). Note that direction of migration is always indicated forward in time throughout the text, including for coalescent simulations.
In the simulations, models with populations connected only by migration (bidirectional migration and unidirectional migration from P2 to P1) were detected at all differentiation levels, though the power was higher with higher levels of genetic differentiation (Figure 2B). Unlike the R_{ F } statistic, a minimum recombination rate is not necessary and the simulations without recombination show some (low) power to detect directional migration (Figure 3B). This might be due to a pattern produced by an asymmetry in the populations since higher polymorphism in the sink population than in the source population is expected. Still, recombination plays an important role for this statistic since its power increases with recombination. It is interesting to note that the presence of S sites for the highest differentiation levels considered was very low or null. Therefore, the values of the W_{ x1s2 } statistic depend only on the distribution of X_{1} and X_{2} sites and the orientation of the mutations is not required.
Detection of migration within the Drosophila simulansspecies complex
Description of genetics markers and number of sequences used in the Drosophila analyses
Locus | Chromosomal location | Maximum length | Number of sequences | |||
---|---|---|---|---|---|---|
D. simulans | D. sechellia | D. mauritiana(Mauritius Is.) | D. mauritiana(Rodrigues Is.) | |||
amyrel | 2R | 1598 | 38 | 88 | 48 | 38 |
joc | 3R | 702 | 46 | 63 | 48 | 38 |
notch | X | 1092 | 29 | 30 | 43 | 24 |
obp 57d/e | 2R | 2039 | 38 | 54 | 24 | 16 |
odysseus | X | 843 | 30 | 29 | 37 | 25 |
otu | X | 1394 | 31 | 83 | 37 | 25 |
period | X | 616 | 38 | 94 | 38 | 24 |
pgd | X | 2323 | 31 | 79 | 37 | 25 |
sqh | X | 1816 | 30 | 82 | 37 | 24 |
vermilion | X | 1477 | 32 | 85 | 37 | 24 |
white | X | 1248 | 31 | 82 | 43 | 25 |
Mutation and recombination parameter estimates
D. simulans | D. sechellia | D. mauritiana | ||||||
---|---|---|---|---|---|---|---|---|
Mauritius Is. | Rodrigues Is. | |||||||
${\stackrel{\u02c6}{\mathbf{\theta}}}_{\mathbf{\pi}}$ | $\widehat{\mathbf{\rho}}$ | ${\widehat{\mathbf{\theta}}}_{\mathbf{\pi}}$ | $\widehat{\mathbf{\rho}}$ | ${\widehat{\mathbf{\theta}}}_{\mathbf{\pi}}$ | $\widehat{\mathbf{\rho}}$ | ${\widehat{\mathbf{\theta}}}_{\mathbf{\pi}}$ | $\widehat{\mathbf{\rho}}$ | |
amyrel | 39.85 | 37.62 | 1.78 | 24.63 | 18.65 | >100 | 19.73 | 33.08 |
joc | 12.97 | >100 | 0.09 | n.a. | 10.56 | >100 | 6.02 | 4.15 |
notch | 27.01 | 78.35 | 0.64 | 5.85 | 7.12 | >100 | 5.62 | 2.78 |
obp 57d/e | 68.39 | 47.41 | 0.90 | 1.33 | 20.02 | >100 | 17.45 | 16.64 |
odysseus | 5.72 | 8.36 | 1.54 | 1.55 | 3.03 | 9.33 | 0.73 | 1.10 |
otu | 15.47 | 37.45 | 0.93 | 6.79 | 10.11 | >100 | 6.01 | 8.4 |
period | 10.12 | 74.82 | 0.73 | >100 | 4.63 | >100 | 4.15 | 1.27 |
pgd | 24.07 | 92.35 | 1.79 | 5.53 | 18.51 | >100 | 9.27 | 1.97 |
sqh | 20.99 | 53.87 | 1.67 | 10.04 | 17.57 | 71.64 | 14.46 | 9.21 |
vermilion | 21.63 | >100 | 0.32 | 14.93 | 16.62 | >100 | 12.33 | 0.53 |
white | 15.07 | 85.56 | 1.42 | 0.03 | 7.13 | >100 | 6.86 | 0.42 |
Pairwise genetic differentiation between species and clustering-detection statistics
D ^{ a } | R _{ F } | p-value | W _{x2 s1} | p-value | W _{x1 s2} | p-value | |
---|---|---|---|---|---|---|---|
A D. simulans (P1) & D. mauritiana Mauritius Is. (P2) | |||||||
amyrel | 11.11 | 1 | n.a. | 0.50 | 0.31 | 0.58 | 0.57 |
joc | 2.95 | 1 | n.a. | 0.59 | 0.06 | 0.54 | 0.38 |
notch | 7.60 | 1 | n.a. | 0.51 | 0.28 | 0.57 | 0.59 |
obp 57d/e | 45.71 | 25 | 0.35 | 0.50 | 0.16 | 0.80 | 0.44 |
odysseus | 13.76 | 12 | 0.02 | 0.50 | 0.55 | 0.54 | 0.60 |
otu | 16.46 | 3 | 0.03 | 0.52 | 0.50 | 0.56 | 0.22 |
period | 4.76 | 3 | 0.66 | 0.53 | 0.12 | 0.68 | 0.33 |
pgd | 4.92 | 1 | n.a. | 0.55 | 0.18 | 0.51 | 0.57 |
sqh | 10.33 | 3 | 0.40 | 0.53 | 0.13 | 0.59 | 0.66 |
vermilion | 5.99 | 1 | n.a. | 0.48 | 0.54 | 0.55 | 0.74 |
white | 5.69 | 1 | n.a. | 0.55 | 0.06 | 0.65 | 0.08 |
B D. simulans (P1) & D. mauritiana Rodrigues Is. (P2) | |||||||
amyrel | 16.61 | 7 | 0.78 | 0.48 | 0.41 | 0.75 | 0.55 |
joc | 3.96 | 1 | n.a. | 0.53 | 0.04 | 0.77 | 0.62 |
notch | 8.17 | 1 | n.a. | 0.37 | 0.73 | 0.77 | 0.58 |
obp 57d/e | 45.71 | 25 | 0.38 | 0.47 | 0.36 | 0.87 | 0.51 |
odysseus | 13.80 | 12 | 0.02 | 0.63 | 0.01 | 0.90 | 0.51 |
otu | 17.60 | 2 | 0.0004 | 0.4 | 0.53 | 0.83 | 0.28 |
period | 4.46 | 1 | n.a. | 0.37 | 0.69 | 0.80 | 0.54 |
pgd | 6.83 | 1 | n.a. | 0.44 | 0.33 | 0.78 | 0.41 |
sqh | 11.52 | 5 | 0.46 | 0.43 | 0.56 | 0.86 | 0.27 |
vermilion | 10.80 | 5 | 0.71 | 0.51 | 0.07 | 0.83 | 0.52 |
white | 5.47 | 1 | n.a. | 0.33 | 0.90 | 0.81 | 0.29 |
C D. simulans (P1) & D. sechellia (P2) | |||||||
amyrel | 32.17 | 31 | 0.71 | 0.46 | 0.19 | 0.95 | 0.70 |
joc | 11.42 | 7 | 0.08 | 0.36 | 0.30 | 0.98 | 0.40 |
notch | 9.82 | 3 | 0.02 | 0.41 | 0.20 | 0.97 | 0.35 |
obp 57d/e | 24.88 | 19 | 0.75 | 0.40 | 0.32 | 0.97 | 0.59 |
odysseus | 14.11 | 1 | n.a. | 0.40 | 0.29 | 0.87 | 0.60 |
otu | 17.15 | 23 | 0.75 | 0.33 | 0.48 | 0.95 | 0.48 |
period | 6.19 | 5 | 0.58 | 0.30 | 0.72 | 0.89 | 0.59 |
pgd | 18.08 | 1 | n.a. | 0.45 | 0.13 | 0.95 | 0.54 |
sqh | 9.53 | 1 | n.a. | 0.36 | 0.35 | 0.97 | 0.57 |
vermilion | 16.60 | 18 | 0.63 | 0.36 | 0.33 | 0.97 | 0.75 |
white | 10.82 | 9 | 0.63 | 0.45 | 0.15 | 0.94 | 0.52 |
Pairwise genetic differentiation between populations of D. mauritiana ^{ a } and clustering-detection statistics
D ^{ b } | W _{ x2s1 } | p-value | W _{ x1s2 } | p-value | |
---|---|---|---|---|---|
amyrel | 3.59 | 0.72 | 0.39 | 0.49 | 0.29 |
joc | 0.71 | 0.81 | 0.42 | 0.48 | 0.16 |
notch | 1.11 | 0.79 | 0.23 | 0.44 | 0.52 |
obp 57d/e | 0.78 | 0.79 | 0.01 | 0.58 | 0.01 |
odysseus | 0.15 | 0.94 | 0.35 | 0.59 | 0.04 |
otu | 2.09 | 0.83 | 0.62 | 0.36 | 0.75 |
period | 0.47 | 0.65 | 0.58 | 0.41 | 0.63 |
pgd | 1.99 | 0.80 | 0.33 | 0.42 | 0.49 |
sqh | 0.92 | 0.81 | 0.27 | 0.38 | 0.89 |
vermilion | 3.78 | 0.88 | 0.28 | 0.41 | 0.54 |
white | 1.00 | 0.73 | 0.35 | 0.47 | 0.30 |
We found some evidence, though not definitive, for migration between D. simulans and its two sister species. The R_{ F } statistic was significant for two loci (of five testable loci, Table 3; note that absence of one site category implies that there is a single run) for the D. simulans/D. mauritiana from Mauritius Island (Mau) pair; for two loci (of six) for the D. simulans/D. mauritiana from Rodrigues Island (Rod) pair; and for one locus (of eight) for the D. simulans/D. sechellia pair. Additional support came from the W statistic (note that in this case it will be considered uninformative for the direction since unequal population sizes were assumed in the null model): the two loci had significant W_{x2s1} values for the D. simulans/Rod pair. Our results, based on the spatial arrangement of polymorphisms, are consistent with a genome-wide comparison of one individual from D. simulans, D. sechellia and D. mauritiana, which shows that both autosomal and X-linked regions present a signal consistent with recent introgressions between D. simulans and the two endemic species [16]. Other studies based on smaller genomic regions have revealed that introgression was likely to have occured between D. simulans and Mau both at the mitochondrial and at the nuclear level [16, 27, 39], but our analyses are the first to suggest that introgression may also have occurred between D. simulans and Rod. D. simulans is absent from both Mauritius and Rodrigues although very common in the neighbouring island of La Réunion ([40]; D. Legrand, D. Lachaise and M-L Cariou unpublished observations). Thus, recent introgression may have two non-exclusive origins: (i) D. simulans was present on Mauritius and Rodrigues and recently disappeared and (ii) in the recent past, D. simulans arrived to both islands through human activities, fruit dispersal or climatic factors. The latter scenario opens the possibility that the D. mauritiana gene pool may have absorbed occasional or regular waves of D. simulans dispersers, without the stable presence of a separate D. simulans population on Mauritius. Notice that the shared history of the two mauritiana taxa [27] can also explain the presence of simulans-like alleles in Rod as a consequence of introgression from D. simulans into Mau that occurred before the split of the two D. mauritiana populations about 100,000 years ago. The situation between D. simulans and D. sechellia is different because the two species coexist on the Seychelles archipelago, and a few morphological hybrids of D. simulans-D. sechellia have been observed (D. Lachaise, personal communication).
The intraspecific comparison of the two populations of D. mauritiana (Table 4) cannot benefit from the information provided by R_{ F } statistic since the absence of fixed differences prevents its calculation. However, one of eleven W_{ x2s1 } statistics was significant, and two of eleven W_{ x1s2 } were significant, which provides some evidence that points towards the presence of gene flow. Likelihood-based inferences under the Isolation with Migration model have previously suggested the presence of limited gene flow from Mau to Rod [27].
Conclusions
This works confirms the prediction that the spatial arrangement of polymorphisms along a recombining stretch of a genome is affected by the presence and direction of gene flow. Two summary statistics are described that are sensitive to the spatial clustering of polymorphic sites generated by gene flow, and which can be used in a test to reject the Isolation model as null hypothesis. A third statistic is described that has a distinct behaviour in the presence of migration, but that was not adequate for the test-based approach described in this work. The interest of these statistics is that they are applicable to datasets with characteristics that prevent their analysis with current available programs such as IM [41], because of the presence of intragenic recombination, or MIMAR [8], because of the absence of fixed differences and shared polymorphisms at the same time. However, these statistics should not be seen as a substitution of those methods but rather as a complement. They allow the extraction of information from data that derives from linkage disequilibrium among alleles from recombining loci. This is information that is usually lost when IMa is applied to short sequences (length selected to assure lack of recombination within them) or in likelihood-free methods (such as approximate Bayesian computation, ABC) that do not use heavy computing LD summary statistics. These statistics can be applied to an entire dataset as a previous step before applying IMa to a reduced dataset. They may also be useful as summary statistics in the ABC framework; like the variance of pairwise differences that have low power when applied as a test [3] but have proved useful for ABC [42].
Another advantage of the statistics described in this work is that genotypes do not need to be phased nor individual genotypes identified, because the statistics depend only on the spatial location of sites not on the allelic identity of individuals. Unphased sequence data or sequence data from pooled samples of several individuals (pooling within each population) should be as informative as phased resequencing data (regarding the presently discussed statistics). Another advantage is that knowledge of allele frequencies or the ancestral state is not necessary (although W_{ x1s2 } was described using this information to classify s_{1} and s_{2} sites, the statistic may be calculated exclusively from X_{1} and X_{2} sites, as discussed above). This could be particularly helpful for the study of next generation sequencing data derived from pooled individuals e.g. [43], where the number of individuals sequenced at each polymorphic site and each allelic state is unknown and methods based on the PAC-likelihood or the length of shared haplotypes cannot be applied. As long as the coverage of the sequencing is enough to determine whether the site is polymorphic in each population, R and W statistics may be calculated.
The application of these statistics to the species of the D. simulans complex was illustrative. Although the high recombination rates (Table 2) make it an especially favourable case study for the application of these summary statistics, the results were not as compelling as they could have been. The results suggest genetic exchange between species and also between populations, that is, in the absence of any fixed differences. This conclusion is also supported by several independent studies on this system. The confirmation of the presence of gene flow is an important key for the understanding of the evolution of these species. However, we could not ascertain the presence and direction of migration due to limited power of our statistics in case of unequal population sizes. Resolving issue will be a major step toward a better comprehension of the evolutionary history of the simulans complex.
Methods
Models and simulations
Significance of each observed statistic was estimated from the distribution of the statistic under the null model (isolation model). The distribution of the test statistic was obtained by coalescent simulation [44] with recombination, with parameter values estimated from the data (see below). The isolation model (see Additional file 1: Figure S1) consists of two populations (P1 and P2, with same effective size), with no exchange of migrants, that have diverged for a period of time from a common ancestral population (with effective size equal to that of the present day populations). This model is characterized by three parameters: (i) the population-scaled mutation rate θ = 4Nμ (where N is the effective population size and μ is the mutation rate per locus per generation), (ii) the population-scaled time of divergence T = t/(2 N) (where t is the divergence time expressed in generations), and (iii) the population-scaled recombination rate ρ = 4Nc (where c is the recombination rate per locus per generation). Parameters θ and T for this model were estimated from the data by using the average number of pairwise differences within (d_{ x } and d_{ y }) and between (d_{ xy }) populations [3]. Recombination parameter for Drosophila data was estimated with LDhat ([45]; see below) while the true value was taken for simulated data (assuming a good estimate could be obtained, since properly applying LDhat for each simulation was computationally infeasible). In some instances, a more complex null model was also used with unequal population sizes. This model has one scaled mutation rate parameter for each population (θ_{1}, θ_{2} and θ_{ A }, respectively for populations P1, P2 and ancestral; note that in all our simulations θ_{ A } = θ_{1}). When unequal population sizes were used as the null model, parameter values were estimated from the number of F, S, X_{1} and X_{2} sites [30] with J. Hey’s Sites software (http://bio.cst.temple.edu/~hey/software/software.htm). Sites software numerically solves the equations of the expected number of F, S, X_{1} and X_{2} sites in function of θ_{1}, θ_{2}, θ_{ A } and T for the observed number of F, S, X_{1} and X_{2} sites.
Power and the false positive rate of the proposed statistics were evaluated on datasets generated with coalescent simulations. Six demographic models were used for this evaluation: the isolation (I), migration (M), unidirectional migration (UM), isolation-with-migration (IM), isolation-with-unidirectional-migration (IUM) and panmictic population (P) models (see Additional file 1: Figure S1). The isolation model is as described above. The migration model (also known as two-island model) consists of two populations (with the same effective size) that have never been in contact except for a constant rate of symmetric migration. The parameters of this model are: (i) the population-scaled mutation rate θ, (ii) the population-scaled migration rate M = 4 Nm (where m is the migration rate per generation), and (iii) the population-scaled recombination rate ρ. The unidirectional migration model is the same as the migration model, but with migration only occurring from one population to the other. The isolation-with-migration and -with-unidirectional-migration are intermediate models with both parameters of divergence (T) and migration (M), with migration occurring between the two derived populations after the split of the ancestral population. The panmictic population corresponds to a single population of size θ with a sample of genes divided randomly in two. Unequal population size was also considered for I, M and UM models (see Additional file 1: Figure S2), requiring an additional parameter for each population (scaled mutation rates θ_{1} and θ_{2}).
For each model, at least 14,000 pseudo-samples were generated by coalescent simulation with ms[44]. Each pseudo-sample consisted of a sample of 40 gene copies for each population (in the panmictic model 80, divided into two groups). Mutations were simulated according to an infinitely-many sites mutation model. Parameter values were fixed for scaled mutation and recombination rates to θ = 10 and ρ = 10 for the first set of simulations. Divergence time and migration rate parameter values were taken randomly from the intervals (0.004–40) for M and (0.0125–125) for T (see Additional file 1: Table S1). The range of values used for M and T allowed for simulations with a range of genetic differentiation representing from low-divergence populations of the same species (D ≈ 0) to highly differentiated species (D ≈ 300), and also similar levels of differentiation between divergence and migration models. A second set of simulations was produced to study the effect of recombination rate. For these simulations only I, M and UM models were used. Migration rate was fixed to M = 0.04 and divergence time to T = 12.5 (expected D = 135, for I and M models without recombination [3]). Recombination rate (ρ) took the following values: 0, 0.1, 0.2, 0.3, 0.6, 1, 2, 3, 6, 10, 20, 30, 60, 100, 200 and 300 (with 1000 simulations for each value) (see Additional file 1: Table S2). A third set of simulations was produced to study the effect of unequal population size. For these simulations only I, M and UM models were used. Migration rate was fixed to M = 0.04, divergence time to T = 12.5, recombination rate to ρ = 100 and scaled mutation rate for population P1 to θ_{1} = 10. Scaled mutation rate for population P2 to (θ_{2}) took the following values: 0.1, 0.2, 0.3, 0.6, 1, 2, 3, 6 and 10 (with 1000 simulations for each value) (see Additional file 1: Table S3).
The differentiation statistic D = d_{ xy }-(d_{ x } + d_{ y })/2 (often referred to as Nei’s net distance or D_{ a }[35]) was calculated for each simulation to compare simulations from different models (and experimental data) with similar levels of differentiation. Polymorphic sites were classified into categories (i.e. F, S, X_{1} and X_{2}; f_{1}, f_{2}, s_{1}, s_{2}, x_{1}, x_{2}, f_{2}x_{1} and f_{1}x_{2}) and the statistics R_{ F }, R_{ S }, W_{ x1s2 } and W_{ x2s1 } were calculated from the alignment for each replicate. Power and false positive rates were calculated as the proportion of significant tests (with nominal level α = 0.05) under the different models. For the detection of migration with R_{ F } and R_{ S } statistics, M, UM, IM and IUM models were used to estimate power and I model (the null model) was used to estimate the false positive rate; while for the detection of unidirectional migration with W_{x1s2} statistic, M, UM (from P2 to P1), IM and IUM (from P2 to P1) models were used to estimate power and I, UM (from P1 to P2) and IUM (from P1 to P2) models were used to estimate the false positive rate. For the first set of simulations, power and false positive rate were estimated as a function of D (for each value D_{ i } of D from the simulations, all simulations with D_{ j } within interval [D_{ i }-0.2D_{ i }, D_{ i } + 0.2D_{ i }] were used to estimate to estimate power at D = D_{ i }, provided there were at least 100 simulations within the interval). The proportion of significant tests for D_{ i } was estimated from the simulations from the above-defined interval using a weighted (using an Epanechnikov kernel) logistic regression. For the other simulations the observed proportion of significant tests for each pre-set value of ρ or θ_{1}/θ_{2} ratio was used. All computations were done in R [46] and the scripts are available from M. Navascués upon request.
Drosophila simulansspecies complex
The statistics described above were applied to populations and species of the D. simulans complex in order to test for introgression between D. sechellia and D. simulans, between the two populations of D. mauritiana and D. simulans, and within D. mauritiana (Mauritius and Rodrigues populations). We specifically wanted to distinguish between the hypotheses of an absence of gene flow between all pairs of species, similar exchanges between the species or unidirectional gene flow (this later objective could not be addressed as discussed above). We extended datasets of D. sechellia and D. mauritiana used in previous studies [25, 27] to construct a larger set of sequences which includes D. simulans and additional markers. D. simulans flies were representative of the species and primarily from its region of origin. They were from Madagascar, the Seychelles archipelago, Comoros, La Réunion, South Africa, Uganda, Tanzania and Annobon Island (Guinean gulf, West Africa; Additional file 1: Figure S4). D. sechellia flies originated from Aride, Denis, Silhouette, Coco, Cousin, Cousine, Frégate, Mahé and Praslin islands of the Seychelles archipelago. Finally, the D. mauritiana sample consisted of two distant populations, the Mau population from Mauritius and the Rod population from the island of Rodrigues, as in [27]. Flies were collected from the wild and directly conserved in absolute alcohol until sequencing, with the exception of some D. simulans lines from Madagascar and Comoros that have been kept in the laboratory for 20 to 200 generations. Experimental procedures comply with institutional, national and international ethical guidelines. Drosophila were collected with the permission of the National Parks and Conservation Service of the Ministry of Agro Industry Food Production and Security of Mauritius, the Ministry of Environment and conservation department of the Seychelles, The Ministry of Environnement of Madagascar. The global dataset consisted of 11 nuclear genes, amyrel, joc, notch, obp57d/e, odysseus, otu, period, pgd, sqh, vermilion and white, representing a total of 15 kb, for at least 29 gene copies per species (Table 1). Sequencing was performed following [25] and primers for each locus and each species are available upon request. Sequences were aligned by visual inspection using Bioedit v7.0.9.0; estimates of the scaled recombination rate, ρ, for each locus and taxon were performed by the composite likelihood method implemented in LDhat [45] (for estimates of ρ > 100 a value of ρ = 100 was used in the null hypothesis), and estimates of scaled mutation rate from nucleotide polymorphism, θ_{ π }, were computed with DnaSP v5 [47]. Polymorphic sites were classified in categories (i.e. F, S and X; s_{1}, s_{2}, x_{1}, x_{2}, f_{2}x_{1} and f_{1}x_{2}), and the statistics R_{ F }, R_{ S }, W_{ x2s1 } and W_{ x1s2 } were calculated from the alignments. Given the clear differences in size among populations, significance of the statistics was tested using the isolation models with unequal population sizes as null model. Ancestral and derived states were deduced by the use of D. melanogaster as an outgroup, for which sequences were obtained from the whole genome of D. melanogaster available in GenBank under the following accession numbers: AE014298 (chromosome X), AE013599 (chromosome 2R), AE014297 (chromosome 3R). The Drosophila sequence data set supporting the results of this article is available in the Dryad Digital Repository, with identifier doi: 10.5061/dryad.67f8v (http://doi.org/10.5061/dryad.67f8v).
Declarations
Acknowledgements
We thank M. Debiais-Thibaud for collecting Drosophila simulans flies from South Africa and C. Biémont for making lines of D. simulans from Madagascar and Comoros available. We thank B. Emerson for correcting and improving the English of this article. The input from several reviewers (in particular one that revised three different versions of the manuscript) contributed to improve the text and the analyses. This work was supported by Agence Nationale de la Recherche, Biodiversity program ANR-06-BDIV-003. DL benefited from membership of the “Laboratoire d’Excellence” TULIP (ANR-10-LABX-41). MN has also been funded by the Jeune Équipe INRA 2010 “Inférence en Génétique et Génomique des Populations”.
Authors’ Affiliations
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