#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Mutation and Evolutionary Rates in Adélie Penguins from the Antarctic


Precise estimations of molecular rates are fundamental to our understanding of the processes of evolution. In principle, mutation and evolutionary rates for neutral regions of the same species are expected to be equal. However, a number of recent studies have shown that mutation rates estimated from pedigree material are much faster than evolutionary rates measured over longer time periods. To resolve this apparent contradiction, we have examined the hypervariable region (HVR I) of the mitochondrial genome using families of Adélie penguins (Pygoscelis adeliae) from the Antarctic. We sequenced 344 bps of the HVR I from penguins comprising 508 families with 915 chicks, together with both their parents. All of the 62 germline heteroplasmies that we detected in mothers were also detected in their offspring, consistent with maternal inheritance. These data give an estimated mutation rate (μ) of 0.55 mutations/site/Myrs (HPD 95% confidence interval of 0.29–0.88 mutations/site/Myrs) after accounting for the persistence of these heteroplasmies and the sensitivity of current detection methods. In comparison, the rate of evolution (k) of the same HVR I region, determined using DNA sequences from 162 known age sub-fossil bones spanning a 37,000-year period, was 0.86 substitutions/site/Myrs (HPD 95% confidence interval of 0.53 and 1.17). Importantly, the latter rate is not statistically different from our estimate of the mutation rate. These results are in contrast to the view that molecular rates are time dependent.


Vyšlo v časopise: Mutation and Evolutionary Rates in Adélie Penguins from the Antarctic. PLoS Genet 4(10): e32767. doi:10.1371/journal.pgen.1000209
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1000209

Souhrn

Precise estimations of molecular rates are fundamental to our understanding of the processes of evolution. In principle, mutation and evolutionary rates for neutral regions of the same species are expected to be equal. However, a number of recent studies have shown that mutation rates estimated from pedigree material are much faster than evolutionary rates measured over longer time periods. To resolve this apparent contradiction, we have examined the hypervariable region (HVR I) of the mitochondrial genome using families of Adélie penguins (Pygoscelis adeliae) from the Antarctic. We sequenced 344 bps of the HVR I from penguins comprising 508 families with 915 chicks, together with both their parents. All of the 62 germline heteroplasmies that we detected in mothers were also detected in their offspring, consistent with maternal inheritance. These data give an estimated mutation rate (μ) of 0.55 mutations/site/Myrs (HPD 95% confidence interval of 0.29–0.88 mutations/site/Myrs) after accounting for the persistence of these heteroplasmies and the sensitivity of current detection methods. In comparison, the rate of evolution (k) of the same HVR I region, determined using DNA sequences from 162 known age sub-fossil bones spanning a 37,000-year period, was 0.86 substitutions/site/Myrs (HPD 95% confidence interval of 0.53 and 1.17). Importantly, the latter rate is not statistically different from our estimate of the mutation rate. These results are in contrast to the view that molecular rates are time dependent.


Zdroje

1. KingJL

JukesTH

1969 Non-Darwinian Evolution. Science 164 788 798

2. PennyD

2005 Relativity for molecular clocks. Nature 436 183 184

3. HoSYW

PhillipsMJ

CooperA

DrummondAJ

2005 Time dependency of molecular rate estimates and systematic overestimation of recent divergence times. Mol Biol Evol 22 1561 1568

4. HoSYW

LarsonG

2006 Molecular clocks: when times are a-changin’. Trends in Genetics 22 79 83

5. ParsonsTJ

MuniecDS

SullivanK

WoodyattN

Alliston-GreinerR

1997 A high observed substitution rate in the human mitochondrial DNA control region. Nat Genet 15 363 368

6. SantosC

MontielR

SierraB

BettencourtC

FernandezE

2005 Understanding differences between phylogenetic and pedigree-derived mtDNA mutation rate: a model using families from the Azores Islands (Portugal). Mol Biol Evol 22 1490 1505

7. HowellN

SmejkalCB

MackeyDA

ChinneryPF

TurnbullDM

2003 The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates. Am J Hum Genet 72 659 670

8. LambertDM

RitchiePA

MillarCD

HollandB

DrummondAJ

2002 Rates of evolution in ancient DNA from Adélie penguins. Science 295 2270 2273

9. LeonardJA

WayneRK

CooperA

2000 Population genetics of ice age brown bears. Proc Natl Acad Sci USA 97 1651 1654

10. ShapiroB

DrummondAJ

RambautA

WilsonMC

MatheusPE

2004 Rise and fall of the Beringian steppe bison. Science 306 1561 1565

11. ShieldsGF

WilsonAC

1987 Calibration of mitochondrial DNA evolution in geese. J Mol Evol 24 212 217

12. WatersJM

DijkstraLH

WallisGP

2000 Biogeography of a southern hemisphere freshwater fish: how important is marine dispersal? Mol Ecol 9 1815 1821

13. PereiraSL

BakerAJ

2006 A mitogenomic timescale for birds detects variable phylogenetic rates of molecular evolution and refutes the standard molecular clock. Mol Biol Evol 23 1731 1740

14. AinleyDG

2002 The Adélie penguin: bellwether of climate change. (Columbia University Press, New York, 2002)

15. ShepherdLD

MillarCD

BallardG

AinleyDG

WilsonPR

2005 Microevolution and mega-icebergs in the Antarctic. Proc Natl Acad Sci USA 102 16717 16722

16. RitchiePA

MillarCD

GibbG

BaroniC

LambertDM

2004 Ancient DNA enables timing of the Pleistocene origin and Holocene expansion of two Adélie penguin lineages in Antarctica. Mol Biol Evol 21 240 248

17. EwingB

GreenP

1998 Base-calling of automated sequencer traces using PHRED. II. Error probabilities. Genome Res 8 186 194

18. AinleyDG

LeRescheRE

SladenWJL

1983 Breeding biology of the Adélie penguin (University of California Press, Berkeley, Los Angeles and London)

19. RandDM

2001 The units of selection on mitochondrial DNA. Annu Rev Ecol Syst 32 415 448

20. BallardJWO

WhitlockMC

2004 The incomplete natural history of mitochondria. Mol Ecol 13 729 744

21. AshleyMV

LaipisPJ

HauswirthWW

1989 Rapid segregation of heteroplasmic bovine mitochondria. Nucleic Acids Res 17 7325 7331

22. BlokRB

GookDA

ThorburnDR

DahlH-HM

1997 Skewed segregation of the mtDNA nt 8993 (T→G) mutation in human oocytes. Am J Hum Genet 60 1495 1501

23. HendyMD

WoodhamsMD

DoddA

2008 Modelling mitochondrial heteroplasmy. Submitted for publication.

24. Weisstein, Eric W. “Sample Variance Distribution.” From MathWorld–A Wolfram Web Resource. http://mathworld.wolfram.com/SampleVarianceDistribution.html

25. DenverDR

MorrisK

LynchM

VassilievaLL

ThomasK

2000 High direct estimate of the mutation rate in the mitochondrial genome of Caenorhabditis elegans. Science 289 2342 2344

26. CaveilierL

JazinE

JalonenP

GyllenstenU

2000 MtDNA substitution rate and segregation of heteroplasmy in coding and noncoding regions. Hum Genet 107 45 50

27. DrummondAJ

RambautA

2003 BEAST version 1.3. Oxford University Press, Oxford. http://beast.bio.ed.ac.uk/

28. NearTJ

SandersonMJ

2004 Assessing the quality of molecular divergence time estimates by fossil calibrations and fossil-based model selection. Phil Trans R Soc Lond B 359 1477 1483

29. SiguroardóttirS

HelgasonA

GulcherJR

StefanssonK

DonnellyP

2000 The mutation rate in the human mtDNA control region. Am J Hum Genet 66 1599 1609

30. EmersonBC

2007 Alarm bells for the molecular clock? No support for Ho et al.'s model of time-dependent molecular rate estimates. Systematic Biology 56 337 345

31. HoSYW

ShapiroB

PhillipsM

CooperA

DrummondA

2007 Evidence for time dependency of molecular rate estimates. Systematic Biology 56 515 522

32. SeutinG

WhiteBN

BoagPT

1991 Preservation of avian blood and tissue samples for DNA analyses. Canadian J Zool 69 82 90

33. WalshPS

MetzgerDA

HiguchiR

1991 Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material. Biotechniques 10 506 513

34. KumarS

TamuraK

NeiM

2004 MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment. Briefings in Bioinformatics 5 150 163

Štítky
Genetika Reprodukčná medicína
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#