- Research article
- Open Access
On the potential for extinction by Muller's Ratchet in Caenorhabditis elegans
© Loewe and Cutter; licensee BioMed Central Ltd. 2008
- Received: 30 October 2007
- Accepted: 30 April 2008
- Published: 30 April 2008
The self-fertile hermaphrodite worm C. elegans is an important model organism for biology, yet little is known about the origin and persistence of the self-fertilizing mode of reproduction in this lineage. Recent work has demonstrated an extraordinary degree of selfing combined with a high deleterious mutation rate in contemporary populations. These observations raise the question as to whether the mutation load might rise to such a degree as to eventually threaten the species with extinction. The potential for such a process to occur would inform our understanding of the time since the origin of self-fertilization in C. elegans history.
To address this issue, here we quantify the rate of fitness decline expected to occur via Muller's ratchet for a purely selfing population, using both analytical approximations and globally distributed individual-based simulations from the evolution@home system to compute the rate of deleterious mutation accumulation. Using the best available estimates for parameters of how C. elegans evolves, we conclude that pure selfing can persist for only short evolutionary intervals, and is expected to lead to extinction within thousands of years for a plausible portion of parameter space. Credible lower-bound estimates of nuclear mutation rates do not extend the expected time to extinction much beyond a million years.
Thus we conclude that either the extreme self-fertilization implied by current patterns of genetic variation in C. elegans arose relatively recently or that low levels of outcrossing and other factors are key to the persistence of C. elegans into the present day. We also discuss results for the mitochondrial genome and the implications for C. briggsae, a close relative that made the transition to selfing independently of C. elegans.
- Mutation Rate
- Effective Population Size
- Deleterious Mutation
- Mutation Load
- Compensatory Mutation
The bactivorous nematode Caenorhabditis elegans is an established model for molecular genetics, development, neurobiology, and, more recently, for evolutionary biology . One of the principal features that distinguishes this species from most of its congeners is the existence of self-fertile hermaphrodites. It is now clear that hermaphrodites evolved from females in at least two Caenorhabditis lineages [2, 3]. However, the age of self-fertilization in C. elegans' history is a longstanding question. The lack of a good fossil record for nematodes means that we must focus on theoretical and molecular methods for inferring the timing of such ancestral events. It is important to acquire a better understanding of how long hermaphrodites have persisted in the C. elegans lineage because a recent versus ancient origin of selfing will strongly influence our inferences from comparative analyses and population genetic patterns, and our interpretations about the adaptive nature of phenotypes. In the present study, we explore this issue by considering the potential for extinction to occur by way of Muller's Ratchet [4–6] in the context of parameters that describe how C. elegans evolves.
Muller's ratchet leads to the stochastic accumulation of slightly deleterious mutations in finite asexual populations [4, 5](for a review see ). This process operates by the sequential loss of the class of individuals in a population that have the highest fitness, resulting in an irrecoverable ratcheting up of the mutation load. In the absence of mitigating factors, this process can lead to population extinction [7–9]. Muller's ratchet also accumulates deleterious mutations in selfers, with the dynamics being described appropriately by a simple rescaling of parameters relative to the asexual case [10–12]. This rescaling allows us to predict the rate of mutation accumulation from Muller's ratchet in selfing organisms by using a methodology established for asexual systems . Consequently, we apply this approach to infer the expected time to extinction by Muller's ratchet for lines of C. elegans under the assumption that outcrossing stopped immediately upon the origin of the self-fertile lineage. Estimates of the effective population size for C. elegans based on genetic variation are generally small [13–16], particularly as compared to related obligately outbreeding species ; this observation reinforces the potential for Muller's ratchet to operate in this system. Because C. elegans populations do undergo low levels of outcrossing in nature, which could ameliorate the effects of Muller's ratchet, this approach provides a benchmark for the time over which C. elegans can persist in a purely self-fertile state.
Two qualitative outcomes may result from such an analysis. (i) The expected extinction times might exceed the time since divergence from the closest outcrossing relative. In this case, we could conclude that Muller's ratchet is an unimportant factor for the persistence of the species subject to selfing, because insufficient time would have elapsed to have resulted in extinction by this process. (ii) The expected time to extinction might be much shorter than the time since divergence from the nearest outcrossing relative. In this case, extinction times provide either an upper limit on the time since the origin of selfing or they indicate that some other biological process, such as outcrossing or compensatory mutation, must occur with sufficient frequency to offset genomic decay in the long term. While a variety of such potential processes are possible (see review in), simpler models are preferable in the absence of evidence supporting their operation.
Here we aim to compute the most plausible estimates for the time to extinction for a lineage of C. elegans that reproduces purely by self-ferilization, based on the standard model of Muller's ratchet described elsewhere [12, 6]. We find that, for a wide range of biologically realistic parameters, Muller's ratchet would have led to extinction in the known time of existence of the lineage leading to C. elegans. Several explanations could reconcile this result with the persistence of this species: (i) nearly complete selfing is a relatively recent innovation in the C. elegans lineage, (ii) a low level of regular outcrossing has been crucial for deleterious mutation elimination in this species history, (iii) outcrossing activity might be concentrated in a few populations that repeatedly give rise to many purely selfing lines that are then distributed around the world, (iv) adaptive or compensatory mutations repair most of the mutational damage, or (v) mutation rates in the wild are much lower than indicated by current evidence. We argue that scenario (i) is most plausible, and therefore propose that the present-day extreme form of self-fertilization seen in this species is likely to have originated relatively recently in evolutionary time, perhaps facilitated or exacerbated by the loss of pheromone attraction between the sexes . However, it remains a formal possibility that low levels of outcrossing, perhaps in combination with other factors, might also play a role in the persistence of self-fertile C. elegans populations.
We estimated the time to extinction of a purely selfing population due to the accumulation of deleterious mutations via Muller's ratchet, based on parameter values for C. elegans. The genomic deleterious mutation rate, U SDM , is the key parameter, which we obtained by scaling estimates of the total genomic mutation rate, U TOT by f SDM , the fraction of slightly deleterious mutations. From U SDM we infer the rate of deleterious mutation accumulation and extrapolate it to the expected extinction times using estimates of C. elegans reproductive capacity and generation time. To infer the rate of mutation accumulation we use analytical approximations [19–21, 6], global computing simulations [6, 22] and an appropriate scaling of the key parameters to accommodate a distribution of mutational effects [6, 12]. In order to account for the fact that C. elegans is selfing and not truly asexual, we also applied a simple transformation to double the magnitude of heterozygous mutational effects, although this has little consequence for our conclusions  as the distribution of mutational effects is very wide on a log-scale [23, 24]. To visualize the results, we use the U-shaped plot of extinction time as a function of the selection coefficient against deleterious mutations (s), to characterize the range of critical selection coefficients s c between which extinction is expected to occur in a given interval of time [6, 9]. This critical range of selection coefficients corresponds to the class of deleterious mutations that are sufficiently weak that they can accumulate, yet are strong enough to negatively impact fitness.
These results indicate either that a predominantly selfing mode of reproduction is a recent innovation in the C. elegans lineage or that compensatory mutation and/or regular bouts of outcrossing contribute to species persistence. For the most plausible estimates of the nuclear deleterious mutation rate we conclude that Muller's ratchet would have led to extinction within thousands of years (tens or hundreds of thousands of generations). More generally, current knowledge about mutation rates and the distribution of deleterious mutational effects (DDME) cannot be reconciled easily with extinction times of more than a million years in the absence of outcrossing.
Segregation in selfers
Previous work has shown that the segregation of deleterious mutations that occurs during meiosis can reduce the rate of mutation accumulation . The same is true for asexual species that experience mitotic recombination [28, 12]. Because recombination can stop Muller's ratchet [11, 29], one might argue that segregation in selfers could be sufficient to halt Muller's ratchet. However, existing theory shows that this would be true only if all mutations have effects of a specific size such that their doubling will shift them into the domain of background selection and thus prevent their accumulation [10–12]. This is not likely to stop Muller's ratchet if there is a broad, continuous distribution of deleterious mutational effects, as is most compatible with our present understanding. If our analysis is corrected for the maximal recombinational repair that can come from free recombination within a selfer [10–12], then it still indicates that Muller's ratchet continues to operate (to apply this correction we use the haploid genomic mutation rate of U SDM = 0.5 instead of the diploid rate of U SDM = 1 in Figure 1). Thus purging of deleterious mutations by segregation in selfers is not expected to stop Muller's ratchet here.
Our analysis of Muller's ratchet assumes pure selfing, yet population genetic studies have demonstrated that outcrossing does occur at low levels in C. elegans [13, 14, 30, 15, 31, 32]. However, recent evidence of outbreeding depression in C. elegans  and of changes in multilocus haplotype frequencies over time in nature , in which recombinants appear to suffer a fitness disadvantage, indicate that outcrossing and effective recombination are selected against, even if they occur within the same population. In laboratory populations, males and outcrossing are selected against, although elevated mutation rates and some genetic backgrounds partially mitigate this effect [34–38]. Furthermore, females of obligate outcrossing sister species have a pheromone that is attractive to males of all related species, but this has been lost in the selfing species C. elegans and C. briggsae , probably impeding the potential for male C. elegans to successfully locate and inseminate receptive mates in nature. Although there is evidence of some form of attraction of males to hermaphrodite-produced compounds in C. elegans [39, 40], it would appear to be substantially weaker than in gonochoristic species . Hermaphrodite C. elegans are less likely to mate if self-sperm is present in their reproductive tract . Hermaphrodite C. elegans and C. briggsae also fail to exhibit the mate searching exhibited by females of related species [42, 43] and hermaphrodites lack the mating-immobility behaviour that is observed in females of obligate outcrossing species , which will further obstruct successful insemination by males in nature.
These observations inform the potential for alternative causes of population persistence to occur in the face of deleterious mutation accumulation by Muller's ratchet: Is selfing a recent innovation, and rare outcrossing irrelevant to reducing the mutation load? Or, are the low levels of outcrossing sufficient to prevent extinction even over long evolutionary periods of time? Patterns of molecular evolution indicate that the reduction of effective population size observed for selfing Caenorhabditis species is unlikely to have occurred too distantly in the past . The multiple genetic, behavioural, and physiological factors that reinforce selfing behaviour would also appear to favor a recent origin of extreme selfing in C. elegans, but a role for outcrossing in species persistence cannot be ruled out at this point. We also note that a relatively recent origin for extreme self-fertilization does not preclude a period of more moderate selfing rates in the history of breeding system evolution in the lineage leading to C. elegans. However, the large number of factors that reinforce selfing reproduction argue against a simple common transition from frequent outcrossing to highly selfing. Thus it appears unlikely that a few outcrossing source populations of C. elegans ensure long-term species persistence by continuously giving rise to many selfing lines that are doomed to extinction once they stop outcrossing regularly.
Some degree of outcrossing in self-fertile species can be sufficient to stop deleterious mutation accumulation from Muller's ratchet [11, 29]. However, existing simulation results suggest that outcrossing rates of less than 1% do not reduce the rate of mutation accumulation substantially [11, 29]. Thus, further simulations of occasional outcrossing in C. elegans might not yield conclusions that differ strongly from our results. Nevertheless, it is an important, albeit non-trivial, next step to quantitatively assess the potential impact of rare outcrossing events on expected extinction times, especially in combination with other potentially mitigating factors like advantageous mutation.
Distribution of deleterious mutational effects (DDME)
If one were to assume that the DDME of insertions and deletions would result in their deterministic removal by purifying selection, then limiting U to the single nucleotide mutation rate (U SDM ~0.2 vs. 0.5) would result in a somewhat longer expected time to extinction. We would nevertheless still expect extinction of a purely selfing lineage within hundreds of thousands of generations (Figure 1). However, the observation of substantial copy number variation in C. elegans  suggests that it is probably most appropriate to apply a mutation rate calculation that includes indels, as we have done.
Because Muller's ratchet leads to a higher rate of mutation accumulation in selfers compared to outcrossers, one might expect such a signature in the form of increased K A /K S values in C. elegans, when compared to outcrossing sister species . However, such a signature does not appear to robustly describe a selfing versus outcrossing dichotomy [55–57]. This could result from a lack of statistical power, because divergence at effectively neutral and very strongly selected sites will be independent of selfing rates, so only a fraction of sites would be affected. However, the absence of such a signature could also indicate that selfing has a sufficiently recent origin that not enough time has elapsed to accumulate detectable sequence differences.
Even if C. elegans did not experience any outcrossing, other processes might prolong its survival (see the more comprehensive list in ). Several factors warrant further attention.
Lower mutation rates
Many factors influence mutation rates . Although the evidence for the frequency of slightly deleterious mutations is quite robust compared to that in other species, it is difficult to exclude categorically the possibility of lower mutation rates in nature than inferred from the laboratory. However, the similar rates of fitness decline under mutation accumulation for different strains of C. elegans suggest that average mutation rates do not differ greatly among strains with low transposable element loads . Furthermore, one environmental variable, temperature, does not appear to alter mutation rates substantially in this species .
Compensatory and advantageous mutations
Mutation accumulation experiments have found that compensatory mutations arise in C. elegans lines with compromised fitness and that they can increase fitness rapidly . This kind of mutation can effectively compensate for fitness decay from Muller's ratchet  and might be based on variability in quantitative trait loci (QTL) that are not mechanistically related to the mutational damage that they compensate for. If long-term mutation accumulation also degrades the ability for fitness increases at these QTLs, then our results still apply (see also discussion of back mutations in ). Further work is necessary to elucidate the nature of compensatory mutations in C. elegans and a recent study demonstrated that this is possible . Advantageous mutations also are powerful in stopping Muller's ratchet  and these cannot be distinguished from compensatory mutations in a genome that already has experienced a substantial amount of decay. Experimental evolution in viruses indicates that the beneficial mutation rate can increase as fitness declines , which could forestall extinction. However, it remains to be seen whether such a phenomenon is general and could apply to eukaryotes such as C. elegans.
Natural populations of C. elegans show strong structure [13, 14, 16, 32], and metapopulation processes could be important for shaping diversity. Here we assume that these effects are accounted for by using an appropriately scaled effective population size N e that corrects for deviations from panmixis. There is reason to believe that Muller's ratchet basically depends on N e and that other details of population structure can be neglected . Thus our conclusions should not be strongly affected by the presence of structured populations per se in C. elegans. One potential means by which population structure could limit Muller's ratchet is if different demes experience very different outcrossing rates, leading to differential persistence of highly outcrossing demes. Inference from heterozygosity in different samples is suggestive of variable outcrossing rates [15, 14, 30], although both local and global patterns of polymorphism and linkage disequilibrium do not support high outcrossing rates over the long term in this species . The fact that several features of C. elegans biology are specific to the selfing life-style (see above) further argues against the notion that there might be a long-term core of outcrossing populations that facilitate the survival of the species and that constantly produce the selfing lines that are so readily observed. In addition, theory suggests that effective outcrossing rates of less than 1% do not drastically reduce the rate of mutation accumulation [11, 29], thus limiting the potential for transient instances of elevated outcrossing to impact population persistence.
Uncertainty in divergence dates
In concluding that extinction by Muller's ratchet under pure selfing would occur in less time than has elapsed since the common ancestor of C. elegans and its relatives, we applied the divergence time estimates of Cutter . These date estimates are 4- to 6-fold more recent than previous divergence time estimates that assumed a universal molecular clock among mammals, insects, and nematodes [68, 69], and consequently are conservative for our analysis with respect to identifying a genomic decay paradox. Longer divergence times between species make it even less likely that C. elegans could have persisted in a purely selfing state for most of the time since divergence with the Caenorhabditis common ancestor.
We find that Muller's ratchet in mitochondrial DNA operates much slower than deleterious mutation accumulation in nuclear DNA, despite a higher per site mutation rate and taking into account differences in mode of transmission. This is mainly due to the much smaller mutational target of the mitochondrial genome. As a consequence, mutation load of the mitochondrial genome is not expected to be the limiting factor in species persistence for C. elegans. This finding may seem surprising in the light of recent results that found a substantial rate of fitness decay in human mtDNA . However, (i) the shorter extinction times in human mtDNA are mostly due to higher mutation rates, which are probably a consequence of longer generation times, (ii) comparing the same mutation rates shows that absolute nematode extinction times are a bit shorter, as expected from the shorter generation time that makes C. elegans reach the number of generations to extinction quicker, (iii) the overwhelmingly faster speed of genomic decay in nuclear DNA, rather than an absence of decay in mtDNA, makes the mutational load in the nucleus the limiting factor. This conclusion is also robust to the possibility of stronger selection in mtDNA than in nuclear DNA, as our method compares the shortest possible extinction times for all corresponding selection coefficients (stronger selection on mtDNA than assumed will lead to even longer extinction times).
Populations of the sibling species of C. elegans, C. briggsae, also contain a very high fraction of self-fertilizing hermaphrodites. In many respects, C. briggsae shares similar life history characteristics with C. elegans, including levels of polymorphism and linkage disequilibrium, outcrossing rate, generation time, and fecundity . Phenotypic assays of fitness in mutation accumulation lines suggest that C. briggsae might experience a higher mutation rate than C. elegans , although this observation has not yet been confirmed with direct mutation detection. C. briggsae shares a more recent common ancestor with the obligately outbreeding sibling species C. sp. 5 (JU727) than does C. elegans with any known sibling species, so in C. briggsae we can place a more recent upper bound on the time of persistence of self-fertilization (Tage). Sequence divergence suggests that Tage for C. briggsae is roughly 14 My , which implies that this species probably also experiences a genomic decay paradox with respect to Muller's ratchet in the same sense as C. elegans. A deeper sampling of species within the Caenorhabditis phylogeny will help elucidate whether a predominantly selfing mode of reproduction in C. elegans and C. briggsae arose recently in their evolutionary history.
We find that C. elegans life history characteristics and evolutionary parameters are inconsistent with long-term survival as a complete selfer. Therefore, C. elegans' highly selfing lifestyle likely evolved relatively recently in evolutionary time. Alternatively, outcrossing and other factors have played a significant role in maintaining a tolerable mutation load throughout its history. If deleterious mutations are accumulating by Muller's ratchet and C. elegans is on its way to extinction, then the potential for compromised molecular biological phenomena should be taken into consideration in the analysis of C. elegans genetics and development.
Modeling extinction time due to Muller's Ratchet
We use the standard model of Muller's ratchet as described in Loewe  to compute T cl , the time between two clicks of the ratchet, from the effective population size N e , the genomic deleterious mutation rate U SDM , and the selection coefficient against deleterious mutations s (positive s denote deleterious mutations). To account for weaknesses in the various methods of computation, we combine some of the best analytic approximations available [19–21, 6] with individual-based simulations that were computed on the evolution@home global computing network [6, 22]. We also rely on the theoretical work described elsewhere [10–12] to apply these results that were computed for asexuals to selfers. In short, this means doubling selection coefficients (s → 2s) to account for the improved power of selection in selfers and including deleterious mutations from the whole diploid genome (double mutation rate; U SDM and s increases cancel out). This makes the speed of Muller's ratchet in diploid selfers equivalent to the speed in asexual haploids. To account for the presence of a distribution of deleterious mutational effects, we use the appropriate approach as described elsewhere [12, 71]. Briefly, we estimate N e under background selection from diversity data and then use exactly this N e for our simulation, as it has been shown to be appropriate for simulating Muller's ratchet in the presence of background selection without explicitly simulating background selection [12, 71]. We ignore the long-term effects of effectively neutral mutations, as their combined potential for decreasing fitness is too small to be of interest here. Then we scale the total genomic mutation rate U TOT by f SDM , the fraction of slightly deleterious mutations that have critical selection coefficients as determined in Figures 1 and 2 to obtain U SDM . To compute extinction times, we first compute C mm , the number of clicks that are needed for mutational meltdown from C mm = log(1/R max )/log (1 - s), where R max is the maximal reproductive capacity, s is positive for deleterious mutations and fitness is assumed to be multiplicative as in Loewe . The extinction time is then approximated by T ex = C mm * T cl * T gen , where T gen is the absolute generation time.
C. elegans life history and evolutionary parameters
Assumed parameter values for C. elegans as applied to Muller's ratchet models of extinction time
U TOT (nuclear, haploid)
U SDM (nuclear, haploid)
N e (mt)
U TOT (mt)
U SDM (mt)
Many orders of magnitude (10-6 - 1)
Effective population size (Ne) in C. elegans has been estimated from nuclear nucleotide, microsatellite, and amplified fragment length polymorphism (AFLP) diversities to range between 1,000 and 100,000 [13, 14, 16, 15]. The Ne of mtDNA is expected to be equal to the nuclear value in pure selfers . This equalized Ne of mitochondrion and nucleus, relative to the 4:1 expectation for a gonochoristic or dioecious species, is due to (i) a doubling of the mitochondrial effective size because all hermaphrodites can pass mtDNA to their offspring (i.e., lack of males) and (ii) a halving of the nuclear effective size from selfing-induced homozygosity [73, 74]. These estimates can be used directly in our simulations, as they are obtained under background selection .
Maximal reproductive capacity (R max )
The reproductive output of selfing C. elegans is limited by sperm production , and wild isolates vary relatively little in this quantity . Different strains of C. elegans produce from an average of 187 to 353 self-progeny , although mated individuals are capable of producing up to 1000 offspring .
Generation length (T gen )
The generation time of C. elegans in nature is the least well-characterized parameter necessary for the extinction time models. The observation that most animals isolated from nature are found in the "enduring" dauer larval stage suggests that a 2 day generation time with ad libidum food conditions in the laboratory at 25°C is not typical of natural conditions. Dauer larvae can survive up to many months  and mutations exist that extend the lifetime of C. elegans considerably [78, 79]. However, C. elegans dauer larvae are unlikely to be able to survive the long periods that anhydrobiotic species are capable of , because of their unsheathed cuticle . Thus a mean generation time of 30 to 60 days may not be unreasonable. Furthermore, the lack of a long-lived dauer "seed bank" in C. elegans implies that populations cannot be reconstituted by quiescent stage larvae with a low mutation load.
Estimates of the deleterious mutation rate (U SDM ) in C. elegans have been calculated from observable phenotypic declines in fitness in laboratory mutation accumulation lines [82–84] as well as from the direct detection of sequence changes in some of the same mutation accumulation lines [85, 86]. Phenotypic estimates of U SDM have yielded values between 0.0026 and 0.025 deleterious mutations/haploid genome/generation [82–84]. However, Davies et al.  suggest that these measures should be adjusted upward 28-fold because approximately 96% of deleterious mutations are undetectable experimentally, a result that was corroborated with a different approach . Such a correction leads to values of 0.073 and 0.7, respectively. Direct sequencing also suggests a value of U SDM that is about 30 times higher than the initial phenotypic estimate for the same lines . We consider direct sequencing to be more reliable here, as phenotypic mutation accumulation misses many small effects [87, 48]. These effects would have an impact on evolutionary timescales.
The total mutation rate U TOT at potentially deleterious sites can be computed from the observable per base pair mutation rate per generation, μ, and from the mutational target size G. For mitochondria μ mt = 1.6 × 10-7 /bp/generation including indels and 8.9 × 10-8 for point mutations only  with G ≈ 10 Kbp . For nuclear sites μ nu = 2.1 × 10-8 /bp/generation including indels and 9.1 × 10-9 for point mutations only . There are ≈ 26 Mbp in all exons of C. elegans ; this value has to be corrected, since we are not interested in synonymous sites and there are probably about three times more functional sites in noncoding DNA than in coding DNA [91–94], suggesting a total of G ≈ 70 Mbp functional sites per haploid genome. This accords with recent assessments that ~70% of the genome is functional . Thus for the mitochondrial genome U TOT ≈ 0.001/generation and for the haploid nuclear genome U TOT ≈ 1.5/generation (including indels) and U TOT ≈ 0.64/generation (point mutations only).
Distribution of deleterious mutational effects on fitness (DDME)
To estimate U SDM we have to consider (i) the total mutation rate U TOT which is given by the frequency of molecular changes of the DNA and (ii) the corresponding DDME. Information about the DDME is important, because Muller's ratchet would not operate if deleterious mutations all had effects large enough to be eliminated deterministically by selection. Alternatively, mutations could accumulate by Muller's ratchet very rapidly, yet have no effect on fitness, if all mutational effects were sufficiently small. Consequently, we consider extinction time as a function of the strength of selection to identify the range of critical selection coefficients s c that could lead to extinction in a given time interval. We then integrate over all mutational effects to estimate f SDM , the fraction of mutations that have deleterious effects in the range given by s c , so that U SDM = U TOT * f SDM . Although the DDME is largely uncharacterized in C. elegans, we assume here that a substantial proportion of mutational effects are distributed among all the orders of magnitude between lethality (s = 1) and s = 10-6. This assumption appears to be valid in Drosophila, and is likely to be a reasonable approximation for most taxa [23, 24]. Figure 3 can be interpreted as to support this assumption, which uses the calculations of the nonsynonymous to synonymous site divergence ratio (K A /K S ) between C. elegans and C. briggsae from Cutter & Ward . Using this approach it is difficult to see how any particular critical selection coefficients could have f SDM < 10% or f SDM > 50% of U TOT . Therefore, these assumptions about U SDM appear to be justified biologically. This approach is robust to the complicating effects of background selection [71, 97].
We also derived a rough point estimate of the DDME in Caenorhabditis using a method that requires only estimates of replacement (πa) and synonymous-site (πs) diversity for two species [23, 50]. We used estimates of polymorphism for C. elegans and C. remanei. For 40 X-linked loci in C. remanei we use an average πa = 0.00102 and πs = 0.0350 . Comparable measures for C. elegans are more difficult to obtain, because most estimates of nucleotide diversity identify too few replacement site polymorphisms to accurately estimate πa. Heuristically, we use the data of Koch et al.  for this purpose, assuming that their shotgun sequencing randomly sampled the genome with respect to coding and noncoding sequences and that no sequences from each of the 4 strains they sampled overlapped with each other; thus providing a set of single pairwise comparisons with the N2 strain. Using this logic, we compute πa~0.000155 and πs ~ 0.000527 (22 replacement polymorphisms in 1.42 × 105 nonsynonymous basepairs, 25 synonymous polymorphisms in 4.7 × 104 synonymous basepairs). The total number of synonymous and nonsynonymous basepairs was calculated assuming that 26% of the 730 kb sequenced was exonic and that 25% of exonic sites are synonymous, as in the genomic average. We caution that these estimates for C. elegans are not ideal, although we expect that the relative magnitude of πa to πs is reasonable.
Using an approach described elsewhere [23, 50], briefly, we fit lognormal DDME location and shape parameters to the levels of diversity observed for both types of sites in both species. For the above diversity values, μg = 3.86 × 10-4 and σg = 15.76, where μg is the geometric mean mutation rate and σg is the geometric standard deviation. These parameters reflect median central tendency and allow easy computation of the boundaries that include 68% of all probability mass (lower limit = μg/σg; upper limit = μg * σg; μg = exp [arithmetic mean on the log-scale] = median; σg = exp [normal standard deviation on the log-scale]; see ). The resulting point estimate DDME (Figure 4) predicts credible frequencies of dominant lethal mutations if one assumes that Caenorhabditis and Drosophila are roughly similar in this respect . Integrating the ranges of selection coefficients from 10-2 to 0.1, 10-3 to 0.1, and 10-4 to 0.1 results in respective probability masses of f SDM = 9.7%, 34% and 66%. These calculations lend empirical support for the estimates compiled in Table 1.
In order to place the extinction time estimates into a biological context for C. elegans, we use inferences of intraspecific coalescent times within C. elegans and divergence times between C. elegans and its sister taxa. Using the expected coalescent time for a sample of segregating polymorphisms, Cutter  calculated that extant nucleotide polymorphism in this species likely coalesces roughly 60 Kya ago (= 4 N e generations). Maximum persistence times can be inferred from interspecific calculations of the time to the most recent common ancestor (T MRCA ). Previous estimates of T MRCA for C. elegans and its relatives suggested that they diverged 80 – 110 Mya [69, 68], although the use of non-nematode calibration of the molecular clock makes this divergence time almost surely a drastic overestimate [99, 2]. Consequently, we prefer to use some recent dates of divergence using internal calibration , which suggest that C. elegans shared a most recent common ancestor with its outcrossing sister clade approximately 18 Mya (range 5 – 30 Mya). Use of this more recent divergence time is conservative for our purposes as it minimizes the potential of falsely inferring that the expected extinction time is shorter than lineage age.
Special thanks go to the more than 300 participants of evolution@home (especially to Colin D. Batty, David Corbett and Rechenkraft.net) for more than 80 years of CPU-time that are the basis of this analysis. We thank B. Charlesworth, E. Dolgin, P. Keightley and two anonymous reviewers for helpful comments on the manuscript. Financial support came from the Leverhulme Trust. The Centre for Systems Biology at Edinburgh is a Centre for Integrative Systems Biology (CISB) funded by the BBSRC and EPSRC.
- Fitch DH: Evolution: an ecological context for C. elegans. Curr Biol. 2005, 15: R655-658. 10.1016/j.cub.2005.08.028.View ArticlePubMedGoogle Scholar
- Kiontke K, Gavin NP, Raynes Y, Roehrig C, Piano F, Fitch DH: Caenorhabditis phylogeny predicts convergence of hermaphroditism and extensive intron loss. Proc Natl Acad Sci USA. 2004, 101: 9003-9008. 10.1073/pnas.0403094101.PubMed CentralView ArticlePubMedGoogle Scholar
- Cho S, Jin SW, Cohen A, Ellis RE: A phylogeny of Caenorhabditis reveals frequent loss of introns during nematode evolution. Genome Res. 2004, 14: 1207-1220. 10.1101/gr.2639304.PubMed CentralView ArticlePubMedGoogle Scholar
- Muller HJ: The relation of recombination to mutational advance. Mutat Res. 1964, 1: 2-9.View ArticleGoogle Scholar
- Felsenstein J: The evolutionary advantage of recombination. Genetics. 1974, 78: 737-756.PubMed CentralPubMedGoogle Scholar
- Loewe L: Quantifying the genomic decay paradox due to Muller's ratchet in human mitochondrial DNA. Genet Res. 2006, 87: 133-159. 10.1017/S0016672306008123.View ArticlePubMedGoogle Scholar
- Lynch M, Gabriel W: Mutation load and the survival of small populations. Evolution. 1990, 44: 1725-1737. 10.2307/2409502.View ArticleGoogle Scholar
- Lynch M, Butcher RBD, Gabriel W: The mutational meltdown in asexual populations. J Hered. 1993, 84: 339-344.PubMedGoogle Scholar
- Gabriel W, Lynch M, Bürger R: Muller's ratchet and mutational meltdowns. Evolution. 1993, 47: 1744-1757. 10.2307/2410218.View ArticleGoogle Scholar
- Heller R, Maynard Smith J: Does Muller's ratchet work with selfing?. Genet Res. 1978, 32: 289-293.View ArticleGoogle Scholar
- Charlesworth D, Morgan MT, Charlesworth B: Mutation accumulation in finite outbreeding and inbreeding populations. Genet Res. 1993, 61: 39-56.View ArticleGoogle Scholar
- Loewe L, Lamatsch D: Quantifying the threat of extinction from Muller's ratchet in the Amazon molly (Poecilia formosa). BMC Evol Biol. 2008, 8: 88-10.1186/1471-2148-8-88.PubMed CentralView ArticlePubMedGoogle Scholar
- Cutter AD: Nucleotide polymorphism and linkage disequilibrium in wild populations of the partial selfer Caenorhabditis elegans. Genetics. 2006, 172: 171-184. 10.1534/genetics.105.048207.PubMed CentralView ArticlePubMedGoogle Scholar
- Barriere A, Felix MA: High local genetic diversity and low outcrossing rate in Caenorhabditis elegans natural populations. Curr Biol. 2005, 15: 1176-1184. 10.1016/j.cub.2005.06.022.View ArticlePubMedGoogle Scholar
- Sivasundar A, Hey J: Sampling from natural populations with RNAi reveals high outcrossing and population structure in Caenorhabditis elegans. Curr Biol. 2005, 15: 1598-1602. 10.1016/j.cub.2005.08.034.View ArticlePubMedGoogle Scholar
- Sivasundar A, Hey J: Population genetics of Caenorhabditis elegans: the paradox of low polymorphism in a widespread species. Genetics. 2003, 163: 147-157.PubMed CentralPubMedGoogle Scholar
- Cutter AD, Baird SE, Charlesworth D: High nucleotide polymorphism and rapid decay of linkage disequilibrium in wild populations of Caenorhabditis remanei. Genetics. 2006, 174: 901-913. 10.1534/genetics.106.061879.PubMed CentralView ArticlePubMedGoogle Scholar
- Chasnov JR, So WK, Chan CM, Chow KL: The species, sex, and stage specificity of a Caenorhabditis sex pheromone. Proc Natl Acad Sci USA. 2007, 104: 6730-6735. 10.1073/pnas.0608050104.PubMed CentralView ArticlePubMedGoogle Scholar
- Gessler DDG: The constraints of finite size in asexual populations and the rate of the ratchet. Genet Res. 1995, 66: 241-253.View ArticlePubMedGoogle Scholar
- Stephan W, Chao L, Smale JG: The advance of Muller's ratchet in a haploid asexual population: Approximate solutions based on diffusion theory. Genet Res. 1993, 61: 225-231.View ArticlePubMedGoogle Scholar
- Stephan W, Kim Y: Recent applications of diffusion theory to population genetics. Modern developments in theoretical population genetics. Edited by: Slatkin M, Veuille M. 2002, Oxford: Oxford University Press, 72-93.Google Scholar
- Loewe L: Evolution@home: observations on participant choice, work unit variation and low-effort global computing. Softw Pract Exper. 2007, 37: 1289-1318. 10.1002/spe.806.View ArticleGoogle Scholar
- Loewe L, Charlesworth B: Inferring the distribution of mutational effects on fitness in Drosophila. Biol Lett. 2006, 2: 426-430. 10.1098/rsbl.2006.0481.PubMed CentralView ArticlePubMedGoogle Scholar
- Eyre-Walker A, Keightley PD: The distribution of fitness effects of new mutations. Nat Rev Genet. 2007, 8: 610-618. 10.1038/nrg2146.View ArticlePubMedGoogle Scholar
- Piganeau G, Gardner M, Eyre-Walker A: A broad survey of recombination in animal mitochondria. Mol Biol Evol. 2004, 21: 2319-2325. 10.1093/molbev/msh244.View ArticlePubMedGoogle Scholar
- Lunt DH, Hyman BC: Animal mitochondrial DNA recombination. Nature. 1997, 387: 247-10.1038/387247a0.View ArticlePubMedGoogle Scholar
- Antezana MA, Hudson RR: Before crossing over: The advantages of eukaryotic sex in genomes lacking chiasmatic recombination. Genet Res. 1997, 70: 7-25. 10.1017/S0016672397002875.View ArticlePubMedGoogle Scholar
- Omilian AR, Cristescu ME, Dudycha JL, Lynch M: Ameiotic recombination in asexual lineages of Daphnia. Proc Natl Acad Sci USA. 2006, 103: 18638-18643. 10.1073/pnas.0606435103.PubMed CentralView ArticlePubMedGoogle Scholar
- Schultz ST, Lynch M: Mutation and extinction: The role of variable mutational effects, synergistic epistasis, beneficial mutations, and the degree of outcrossing. Evolution. 1997, 51: 1363-1371. 10.2307/2411188.View ArticleGoogle Scholar
- Barriere A, Felix MA: Temporal Dynamics and Linkage Disequilibrium in Natural C. elegans Populations. Genetics. 2007Google Scholar
- Denver DR, Morris K, Thomas WK: Phylogenetics in Caenorhabditis elegans: an analysis of divergence and outcrossing. Mol Biol Evol. 2003, 20: 393-400. 10.1093/molbev/msg044.View ArticlePubMedGoogle Scholar
- Haber M, Schungel M, Putz A, Muller S, Hasert B, Schulenburg H: Evolutionary history of Caenorhabditis elegans inferred from microsatellites: evidence for spatial and temporal genetic differentiation and the occurrence of outbreeding. Mol Biol Evol. 2005, 22: 160-173. 10.1093/molbev/msh264.View ArticlePubMedGoogle Scholar
- Dolgin ES, Charlesworth B, Baird SE, Cutter AD: Inbreeding and outbreeding depression in Caenorhabditis nematodes. Evolution. 2007, 61: 1339-1352. 10.1111/j.1558-5646.2007.00118.x.View ArticlePubMedGoogle Scholar
- Stewart AD, Phillips PC: Selection and maintenance of androdioecy in Caenorhabditis elegans. Genetics. 2002, 160: 975-982.PubMed CentralPubMedGoogle Scholar
- Chasnov JR, Chow KL: Why are there males in the hermaphroditic species Caenorhabditis elegans?. Genetics. 2002, 160: 983-994.PubMed CentralPubMedGoogle Scholar
- Manoel D, Carvalho S, Phillips PC, Teotonio H: Selection against males in Caenorhabditis elegans under two mutational treatments. Proc Biol Sci. 2007, 274: 417-424. 10.1098/rspb.2006.3739.PubMed CentralView ArticlePubMedGoogle Scholar
- Teotonio H, Manoel D, Phillips PC: Genetic variation for outcrossing among Caenorhabditis elegans isolates. Evolution. 2006, 60: 1300-1305.View ArticlePubMedGoogle Scholar
- Cutter AD: Mutation and the experimental evolution of outcrossing in Caenorhabditis elegans. J Evol Biol. 2005, 18: 27-34. 10.1111/j.1420-9101.2004.00804.x.View ArticlePubMedGoogle Scholar
- White JQ, Nicholas TJ, Gritton J, Truong L, Davidson ER, Jorgensen EM: The sensory circuitry for sexual attraction in C. elegans males. Curr Biol. 2007, 17: 1847-1857. 10.1016/j.cub.2007.09.011.View ArticlePubMedGoogle Scholar
- Simon JM, Sternberg PW: Evidence of a mate-finding cue in the hermaphrodite nematode Caenorhabditis elegans. Proc Natl Acad Sci USA. 2002, 99: 1598-1603. 10.1073/pnas.032225799.PubMed CentralView ArticlePubMedGoogle Scholar
- Kleemann GA, Basolo AL: Facultative decrease in mating resistance in hermaphroditic Caenorhabditis elegans with self-sperm depletion. Anim Behav. 2007, 74: 1337-1347.View ArticleGoogle Scholar
- Emmons SW, Lipton J: Genetic basis of male sexual behavior. J Neurobiol. 2003, 54: 93-110. 10.1002/neu.10163.View ArticlePubMedGoogle Scholar
- Lipton J, Kleemann G, Ghosh R, Lints R, Emmons SW: Mate searching in Caenorhabditis elegans: a genetic model for sex drive in a simple invertebrate. J Neurosci. 2004, 24: 7427-7434. 10.1523/JNEUROSCI.1746-04.2004.View ArticlePubMedGoogle Scholar
- Garcia LR, LeBoeuf B, Koo P: Diversity in mating behavior of hermaphroditic and male-female Caenorhabditis nematodes. Genetics. 2007, 175: 1761-1771. 10.1534/genetics.106.068304.PubMed CentralView ArticlePubMedGoogle Scholar
- Cutter AD, Wasmuth JD, Washington NL: Patterns of molecular evolution in Caenorhabditis preclude ancient origins of selfing. Genetics. 2008, 178 (4): 2093-2104. 10.1534/genetics.107.085787.PubMed CentralView ArticlePubMedGoogle Scholar
- Pal C, Papp B, Lercher MJ: An integrated view of protein evolution. Nat Rev Genet. 2006, 7: 337-348. 10.1038/nrg1838.View ArticlePubMedGoogle Scholar
- Kimura M: The neutral theory of molecular evolution. 1983, Cambridge: Cambridge University PressView ArticleGoogle Scholar
- Estes S, Phillips PC, Denver DR, Thomas WK, Lynch M: Mutation accumulation in populations of varying size: the distribution of mutational effects for fitness correlates in Caenorhabditis elegans. Genetics. 2004, 166: 1269-1279. 10.1534/genetics.166.3.1269.PubMed CentralView ArticlePubMedGoogle Scholar
- Charlesworth , Morgan , Charlesworth : Inbreeding depression, genetic load, and the evolution of outcrossing rates in a multilocus system with no linkage. Evolution. 1990, 44: 1469-1489. 10.2307/2409330.View ArticleGoogle Scholar
- Loewe L, Charlesworth B, Bartolomé C, Nöel V: Estimating selection on non-synonymous mutations. Genetics. 2006, 172: 1079-1092. 10.1534/genetics.105.047217.PubMed CentralView ArticlePubMedGoogle Scholar
- Koch R, van Luenen HGAM, van der Horst M, Thijssen KL, Plasterk RHA: Single nucleotide polymorphisms in wild isolates of Caenorhabditis elegans. Genome Res. 2000, 10: 1690-1696. 10.1101/gr.GR-1471R.PubMed CentralView ArticlePubMedGoogle Scholar
- Cutter AD: Multilocus patterns of polymorphism and selection across the X-chromosome of Caenorhabditis remanei. Genetics. 2008, Google Scholar
- Maydan JS, Flibotte S, Edgley ML, Lau J, Selzer RR, Richmond TA, Pofahl NJ, Thomas JH, Moerman DG: Efficient high-resolution deletion discovery in Caenorhabditis elegans by array comparative genomic hybridization. Genome Res. 2007, 17: 337-347. 10.1101/gr.5690307.PubMed CentralView ArticlePubMedGoogle Scholar
- Charlesworth D, Wright SI: Breeding systems and genome evolution. Curr Opin Genet Dev. 2001, 11: 685-690. 10.1016/S0959-437X(00)00254-9.View ArticlePubMedGoogle Scholar
- Cutter AD, Payseur BA: Rates of deleterious mutation and the evolution of sex in Caenorhabditis. J Evol Biol. 2003, 16: 812-822. 10.1046/j.1420-9101.2003.00596.x.View ArticlePubMedGoogle Scholar
- Artieri CG, Haerty W, Gupta BP, Singh RS: Sexual selection and maintenance of sex: Evidence from comparisons of rates of genomic accumulation of mutations and divergence of sex-related genes in sexual and hermaphroditic species of Caenorhabditis. Mol Biol Evol. 2008, doi: doi:10.1093/molbev/msn1046, Google Scholar
- Cutter AD, Wasmuth JD, Washington NL: Patterns of molecular evolution in Caenorhabditis preclude ancient origins of selfing. Genetics. 2008, 178 (4): 2093-2104. 10.1534/genetics.107.085787.PubMed CentralView ArticlePubMedGoogle Scholar
- Baer CF, Miyamoto MM, Denver DR: Mutation rate variation in multicellular eukaryotes: causes and consequences. Nat Rev Genet. 2007, 8: 619-631. 10.1038/nrg2158.View ArticlePubMedGoogle Scholar
- Baer CF, Shaw F, Steding C, Baumgartner M, Hawkins A, Houppert A, Mason N, Reed M, Simonelic K, Woodard W, Lynch M: Comparative evolutionary genetics of spontaneous mutations affecting fitness in rhabditid nematodes. Proc Natl Acad Sci USA. 2005, 102: 5785-5790. 10.1073/pnas.0406056102.PubMed CentralView ArticlePubMedGoogle Scholar
- Baer CF, Phillips N, Ostrow D, Avalos A, Blanton D, Boggs A, Keller T, Levy L, Mezerhane E: Cumulative effects of spontaneous mutations for fitness in Caenorhabditis: role of genotype, environment and stress. Genetics. 2006, 174: 1387-1395. 10.1534/genetics.106.061200.PubMed CentralView ArticlePubMedGoogle Scholar
- Estes S, Lynch M: Rapid fitness recovery in mutationally degraded lines of Caenorhabditis elegans. Evolution. 2003, 57: 1022-1030.View ArticlePubMedGoogle Scholar
- Wagner GP, Gabriel W: Quantitative variation in finite parthenogenetic populations: What stops Muller's ratchet in the absence of recombination?. Evolution. 1990, 44: 715-731. 10.2307/2409447.View ArticleGoogle Scholar
- Howe DK, Denver DR: Muller's Ratchet and compensatory mutation in Caenorhabditis briggsae mitochondrial genome evolution. BMC Evol Biol. 2008, 8: 62-10.1186/1471-2148-8-62.PubMed CentralView ArticlePubMedGoogle Scholar
- Bachtrog D, Gordo I: Adaptive evolution of asexual populations under Muller's ratchet. Evolution. 2004, 58: 1403-1413.View ArticlePubMedGoogle Scholar
- Silander OK, Tenaillon O, Chao L: Understanding the evolutionary fate of finite populations: the dynamics of mutational effects. PLoS Biol. 2007, 5: e94-10.1371/journal.pbio.0050094.PubMed CentralView ArticlePubMedGoogle Scholar
- Combadão J, Campos PRA, Dionisio F, Gordo I: Small-world networks decrease the speed of Muller's ratchet. Genet Res. 2007Google Scholar
- Cutter AD: Divergence times in Caenorhabditis and Drosophila inferred from direct estimates of the neutral mutation rate. Molecular Biology & Evolution. 2008, 25: 778-786. 10.1093/molbev/msn024.View ArticleGoogle Scholar
- Stein LD, Bao Z, Blasiar D, Blumenthal T, Brent MR, Chen N, Chinwalla A, Clarke L, Clee C, Coghlan A, et al: The genome sequence of Caenorhabditis briggsae: a platform for comparative genomics. PLoS Biol. 2003, 1: E45-10.1371/journal.pbio.0000045.PubMed CentralView ArticlePubMedGoogle Scholar
- Coghlan A, Wolfe KH: Fourfold faster rate of genome rearrangement in nematodes than in Drosophila. Genome Res. 2002, 12: 857-867. 10.1101/gr.172702.PubMed CentralView ArticlePubMedGoogle Scholar
- Cutter AD, Felix MA, Barriere A, Charlesworth D: Patterns of nucleotide polymorphism distinguish temperate and tropical wild isolates of Caenorhabditis briggsae. Genetics. 2006, 173: 2021-2031. 10.1534/genetics.106.058651.PubMed CentralView ArticlePubMedGoogle Scholar
- Söderberg RJ, Berg OG: Mutational interference and the progression of Muller's ratchet when mutations have a broad range of effects. Genetics. 2007, 177: 971-986. 10.1534/genetics.107.073791.PubMed CentralView ArticlePubMedGoogle Scholar
- Wright SI, Nano N, Foxe JP, Dar V-uN: Effective population size and tests of neutrality at cytoplasmic genes in Arabidopsis. Genet Res. 2008, 90: 119-128. 10.1017/S0016672307008920.View ArticleGoogle Scholar
- Pollak E: On the theory of partially inbreeding finite populations. I. Partial selfing. Genetics. 1987, 117: 353-360.PubMed CentralPubMedGoogle Scholar
- Nordborg M, Donnelly P: The coalescent process with selfing. Genetics. 1997, 146: 1185-1195.PubMed CentralPubMedGoogle Scholar
- Ward S, Carrel JS: Fertilization and sperm competition in the nematode Caenorhabditis elegans. Developmental Biology. 1979, 73: 304-321. 10.1016/0012-1606(79)90069-1.View ArticlePubMedGoogle Scholar
- Hodgkin J, Doniach T: Natural variation and copulatory plug formation in Caenorhabditis elegans. Genetics. 1997, 146: 149-164.PubMed CentralPubMedGoogle Scholar
- Riddle DL, Blumenthal T, Meyer BJ, Priess JR: 1. Introduction to C. elegans III. Life history and evolution. C elegans II. Edited by: Riddle DL, Blumenthal T, Meyer BJ, Priess JR. 1997, Plainview, New York: Cold Spring Harbor Laboratory Press, [http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=ce2.section.27]Google Scholar
- Arantes-Oliveira N, Berman JR, Kenyon C: Healthy animals with extreme longevity. Science. 2003, 302: 611-10.1126/science.1089169.View ArticlePubMedGoogle Scholar
- Kenyon C, Chang J, Gensch E, Rudner A, Tabtiang R: A C. elegans mutant that lives twice as long as wild type. Nature. 1993, 366: 461-464. 10.1038/366461a0.View ArticlePubMedGoogle Scholar
- McSorley R: Adaptations of nematodes to environmental extremes. Fla Entomol. 2003, 86: 138-142. 10.1653/0015-4040(2003)086[0138:AONTEE]2.0.CO;2.View ArticleGoogle Scholar
- Kiontke K, Sudhaus W: Ecology of Caenorhabditis species. WormBook. Edited by: Fitch DHA. 2006, The C. elegans Research Community, doi/101895/wormbook.1.37.1., [http://www.wormbook.org/]Google Scholar
- Vassilieva LL, Lynch M: The rate of spontaneous mutation for life-history traits in Caenorhabditis elegans. Genetics. 1999, 151: 119-129.PubMed CentralPubMedGoogle Scholar
- Keightley PD, Caballero A: Genomic mutation rates for lifetime reproductive output with lifespan in Caenorhabditis elegans. Proc Natl Acad Sci USA. 1997, 94: 3823-3827. 10.1073/pnas.94.8.3823.PubMed CentralView ArticlePubMedGoogle Scholar
- Keightley PD, Bataillon TM: Multigeneration maximum-likelihood analysis applied to mutation-accumulation experiments in Caenorhabditis elegans. Genetics. 2000, 154: 1193-1201.PubMed CentralPubMedGoogle Scholar
- Denver DR, Morris K, Lynch M, Thomas WK: High mutation rate and predominance of insertions in the Caenorhabditis elegans nuclear genome. Nature. 2004, 430: 679-682. 10.1038/nature02697.View ArticlePubMedGoogle Scholar
- Denver DR, Feinberg S, Estes S, Thomas WK, Lynch M: Mutation rates, spectra, and hotspots in mismatch repair-deficient Caenorhabditis elegans. Genetics. 2005Google Scholar
- Davies EK, Peters AD, Keightley PD: High frequency of cryptic deleterious mutations in Caenorhabditis elegans. Science. 1999, 285: 1748-1751. 10.1126/science.285.5434.1748.View ArticlePubMedGoogle Scholar
- Denver DR, Morris K, Lynch M, Vassilieva LL, Thomas WK: High direct estimate of the mutation rate in the mitochondrial genome of Caenorhabditis elegans. Science. 2000, 289: 2342-2344. 10.1126/science.289.5488.2342.View ArticlePubMedGoogle Scholar
- Okimoto R, Macfarlane JL, Clary DO, Wolstenholme DR: The mitochondrial genomes of two nematodes, Caenorhabditis elegans and Ascaris suum. Genetics. 1992, 130: 471-498.PubMed CentralPubMedGoogle Scholar
- The C. elegans Sequencing Consortium: Genome sequence of the nematode C. elegans: a platform for investigating biology. Science. 1998, 282: 2012-2018. 10.1126/science.282.5396.2012.View ArticleGoogle Scholar
- Webb CT, Shabalina SA, Ogurtsov AY, Kondrashov AS: Analysis of similarity within 142 pairs of orthologous intergenic regions of Caenorhabditis elegans and Caenorhabditis briggsae. Nucleic Acids Res. 2002, 30: 1233-1239. 10.1093/nar/30.5.1233.PubMed CentralView ArticlePubMedGoogle Scholar
- Shabalina SA, Kondrashov AS: Pattern of selective constraint in C. elegans and C. briggsae genomes. Genet Res. 1999, 74: 23-30. 10.1017/S0016672399003821.View ArticlePubMedGoogle Scholar
- Gaffney DJ, Keightley PD: Genomic selective constraints in murid noncoding DNA. PLoS Genetics. 2006, 2: e204-10.1371/journal.pgen.0020204.PubMed CentralView ArticlePubMedGoogle Scholar
- Halligan DL, Keightley PD: Ubiquitous selective constraints in the Drosophila genome revealed by a genome-wide interspecies comparison. Genome Res. 2006, 16: 875-884. 10.1101/gr.5022906.PubMed CentralView ArticlePubMedGoogle Scholar
- He H, Wang J, Liu T, Liu XS, Li T, Wang Y, Qian Z, Zheng H, Zhu X, Wu T, et al: Mapping the C. elegans noncoding transcriptome with a whole-genome tiling microarray. Genome Res. 2007, 17: 1471-1477. 10.1101/gr.6611807.PubMed CentralView ArticlePubMedGoogle Scholar
- Cutter AD, Ward S: Sexual and temporal dynamics of molecular evolution in C. elegans development. Mol Biol Evol. 2005, 22: 178-188. 10.1093/molbev/msh267.View ArticlePubMedGoogle Scholar
- Gordo I, Charlesworth B: The speed of Muller's ratchet with background selection, and the degeneration of Y chromosomes. Genet Res. 2001, 78: 149-161.View ArticlePubMedGoogle Scholar
- Limpert E, Stahel WA, Abbt M: Log-normal distributions across the sciences: Keys and clues. Bioscience. 2001, 51: 341-352. 10.1641/0006-3568(2001)051[0341:LNDATS]2.0.CO;2.View ArticleGoogle Scholar
- Felix MA: Genomes: a helpful cousin for our favourite worm. Curr Biol. 2004, 14: R75-77.View ArticlePubMedGoogle Scholar
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