Molecular clock

Molecular clock
Part of a series on
Evolutionary Biology
Evolutionary tree showing the divergence of modern species from their common ancestor
 
Evolutionary Biology Portal
Category • Related topics • Book
v · d · e

The molecular clock (based on the molecular clock hypothesis (MCH)) is a technique in molecular evolution that uses fossil constraints and rates of molecular change to deduce the time in geologic history when two species or other taxa diverged. It is used to estimate the time of occurrence of events called speciation or radiation. The molecular data used for such calculations is usually nucleotide sequences for DNA or amino acid sequences for proteins. It is sometimes called a gene clock or evolutionary clock.

Contents

Early discovery and genetic equidistance

The notion of the existence of a so-called "molecular clock" was first attributed to Emile Zuckerkandl and Linus Pauling who, in 1962, noticed that the number of amino acid differences in hemoglobin between different lineages changes roughly linearly with time, as estimated from fossil evidence.[1] They generalized this observation to assert that the rate of evolutionary change of any specified protein was approximately constant over time and over different lineages.

The genetic equidistance phenomenon was first noted in 1963 by E. Margoliash, who wrote: "It appears that the number of residue differences between cytochrome C of any two species is mostly conditioned by the time elapsed since the lines of evolution leading to these two species originally diverged. If this is correct, the cytochrome c of all mammals should be equally different from the cytochrome c of all birds. Since fish diverges from the main stem of vertebrate evolution earlier than either birds or mammals, the cytochrome c of both mammals and birds should be equally different from the cytochrome c of fish. Similarly, all vertebrate cytochrome c should be equally different from the yeast protein."[2] For example, the difference between the cytochrome C of a carp and a frog, turtle, chicken, rabbit, and horse is a very constant 13% to 14%. Similarly, the difference between the cytochrome C of a bacterium and yeast, wheat, moth, tuna, pigeon, and horse ranges from 64% to 69%. Together with the work of Emile Zuckerkandl and Linus Pauling, the genetic equidistance result directly led to the formal postulation of the molecular clock hypothesis in the early 1960s.[3] Genetic equidistance has often been used to infer equal time of separation of different sister species from an outgroup.[4][5]

Later Allan Wilson and Vincent Sarich built upon this work.

Relationship with neutral theory

The observation of a clock-like rate of molecular change was originally purely phenomenological. Later, the work of Motoo Kimura[6] developed the neutral theory of molecular evolution, which predicted a molecular clock. Let there be N individuals, and to keep this calculation simple, let the individuals be haploid (i.e. have one copy of each gene). Let the rate of neutral mutations (i.e. mutations with no effect on fitness) in a new individual be μ. The probability that this new mutation will become fixed in the population is then 1/N, since each copy of the gene is as good as any other. Every generation, each individual can have new mutations, so there are μN new neutral mutations in the population as a whole. That means that each generation, μ new neutral mutations will become fixed. If most changes seen during molecular evolution are neutral, then fixations in a population will accumulate at a clock-rate that is equal to the rate of neutral mutations in an individual.

Calibration

The molecular clock alone can only say that one time period is twice as long as another: it cannot assign concrete dates. To achieve this, the molecular clock must first be calibrated against independent evidence about dates, such as the fossil record.[7] Alternatively, for viral phylogenetics and ancient DNA studies, two areas of evolutionary biology where it is possible to sample sequences over an evolutionary timescale, the dates of the samples themselves can be used to calibrate the molecular clock.

Non-constant rate of molecular clock

Sometimes only a single divergence date can be estimated from fossils, with all other dates inferred from that. Other sets of species have abundant fossils available, allowing the MCH of constant divergence rates to be tested. DNA sequences experiencing low levels of negative selection showed divergence rates of 0.7-0.8% per Myr in bacteria, mammals, invertebrates, and plants.[8] In the same study, genomic regions experiencing very high negative or purifying selection (encoding rRNA) were considerably slower (1% per 50 Myr).

In addition to such variation in rate with genomic position, since the early 1990s, variation among taxa has proven fertile ground for research too,[9] even over comparatively short periods of evolutionary time (for example mockingbirds[10]). Tube-nosed seabirds have molecular clocks that on average run at half speed of many other birds,[11] possibly due to long generation times, and many turtles have a molecular clock running at one-eighth the speed it does in small mammals or even slower.[12] Effects of small population size are also likely to confound molecular clock analyses; cheetahs for example, having gone through at least 2 population bottlenecks, could not be adequately studied based on a molecular clock model alone.[citation needed] Researchers such as Ayala have more fundamentally challenged the molecular clock hypothesis.[13][14] According to Ayala's 1999 study, 5 factors combine to limit the application of molecular clock models:

  • Changing generation times (If the rate of new mutations depends at least partly on the number of generations rather than the number of years)
  • Population size (Genetic drift is stronger in small populations, and so more mutations are effectively neutral)
  • Species-specific differences (due to differing metabolism, ecology, evolutionary history,...)
  • Change in function of the protein studied (can be avoided in closely related species by utilizing non-coding DNA sequences or emphasizing silent mutations)
  • Changes in the intensity of natural selection

Molecular clock users have developed workaround solutions using a number of statistical approaches including maximum likelihood techniques and later Bayesian modeling. In particular, models that take into account rate variation across lineages have been proposed in order to obtain better estimates of divergence times. These models are called relaxed molecular clocks[15] because they represent an intermediate position between the 'strict' molecular clock hypothesis and Felsenstein's many-rates model and are made possible through MCMC techniques that explore a weighted range of tree topologies and simultaneously estimate parameters of the chosen substitution model. It must be remembered that divergence dates inferred using a molecular clock are based on statistical inference and not on direct evidence.

The molecular clock runs into particular challenges at very short and very long timescales. At long timescales, the problem is saturation. When enough time has passed, many sites have undergone more than one change, but it is impossible to detect more than one. This means that the observed number of changes is no longer linear with time, but instead flattens out.

At very short time scales, many differences between samples do not represent fixation of different sequences in the different populations. Instead, they represent alternative alleles that were both present as part of a polymorphism in the common ancestor. The inclusion of differences that have not yet become fixed leads to a potentially dramatic inflation of the apparent rate of the molecular clock at very short timescales.[16][17]

Uses

The molecular clock technique is an important tool in molecular systematics, the use of molecular genetics information to determine the correct scientific classification of organisms or to study variation in selective forces.

Knowledge of approximately-constant rate of molecular evolution in particular sets of lineages also facilitates establishing the dates of phylogenetic events, including those not documented by fossils, such as the divergence of living taxa and the formation of the phylogenetic tree. But in these cases — especially over long stretches of time — the limitations of MCH (above) must be considered; such estimates may be off by 50% or more.

See also

References

  1. ^ Zuckerkandl, E. and Pauling, L.B. (1962). "Molecular disease, evolution, and genetic heterogeneity". In Kasha, M. and Pullman, B (editors). Horizons in Biochemistry. Academic Press, New York. pp. 189–225. 
  2. ^ Margoliash E (October 1963). "PRIMARY STRUCTURE AND EVOLUTION OF CYTOCHROME C". Proc. Natl. Acad. Sci. U.S.A. 50 (4): 672–9. doi:10.1073/pnas.50.4.672. PMC 221244. PMID 14077496. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=221244. 
  3. ^ Kumar S (August 2005). "Molecular clocks: four decades of evolution". Nat. Rev. Genet. 6 (8): 654–62. doi:10.1038/nrg1659. PMID 16136655. 
  4. ^ Pesole G, Gissi C, De Chirico A, Saccone C (April 1999). "Nucleotide substitution rate of mammalian mitochondrial genomes". J. Mol. Evol. 48 (4): 427–34. doi:10.1007/PL00006487. PMID 10079281. 
  5. ^ Huang, S. (2008) The genetic equidistance result of molecular evolution is independent of mutation rates. J. Comp. Sci. Syst. Biol., 1: 92-102. http://omicsonline.com/ArchiveJCSB/Ab01/JCSB1.092.html
  6. ^ Kimura, Motoo (1968). "Evolutionary rate at the molecular level". Nature 217 (5129): 624–626. doi:10.1038/217624a0. PMID 5637732. 
  7. ^ benton, M. J. and Donoghue, P. C. J. (200t). "Paleontological evidence to date the Tree of Life". Molecular Biology & Evolution 24 (1): 26–53. doi:10.1093/molbev/msl150. PMID 17047029. 
  8. ^ Ochman H, Wilson AC. (1987). "Evolution in bacteria: evidence for a universal substitution rate in cellular genomes". J Mol Evol. 26 (1–2): 74–86.. doi:10.1007/BF02111283. PMID 3125340. 
  9. ^ Douzery, E.J.P., Delsuc, F., Stanhope, M.J. and Huchon, D. (2003). "Local molecular clocks in three nuclear genes: divergence times for rodents and other mammals, and incompatibility among fossil calibrations". Journal of Molecular Evolution 57: S201–S213. doi:10.1007/s00239-003-0028-x. PMID 15008417. 
  10. ^ Hunt, J.S., Bermingham, E., and Ricklefs, R.E. (2001). "Molecular systematics and biogeography of Antillean thrashers, tremblers, and mockingbirds (Aves: Mimidae)". Auk 118 (1): 35–55. doi:10.1642/0004-8038(2001)118[0035:MSABOA]2.0.CO;2. http://findarticles.com/p/articles/mi_qa3793/is_200101/ai_n8930531. 
  11. ^ Rheindt, F. E. and Austin, J. (2005). "Major analytical and conceptual shortcomings in a recent taxonomic revision of the Procellariiformes - A reply to Penhallurick and Wink (2004)". Emu 105 (2): 181–186. doi:10.1071/MU04039. http://www.publish.csiro.au/?act=view_file&file_id=MU04039.pdf. 
  12. ^ Avise, J.C., Bowen, W., Lamb, T., Meylan, A.B. and Bermingham, E. (1 May 1992). "Mitochondrial DNA Evolution at a Turtle's Pace: Evidence for Low Genetic Variability and Reduced Microevolutionary Rate in the Testudines". Molecular Biology and Evolution 9 (3): 457–473. PMID 1584014. http://mbe.oxfordjournals.org/cgi/reprint/9/3/457. 
  13. ^ Ayala, F.J. (1999). "Molecular clock mirages". BioEssays 21 (1): 71–75. doi:10.1002/(SICI)1521-1878(199901)21:1<71::AID-BIES9>3.0.CO;2-B. PMID 10070256. http://www3.interscience.wiley.com/cgi-bin/abstract/60000186/ABSTRACT?CRETRY=1&SRETRY=0. 
  14. ^ Schwartz, J. H. and Maresca, B. (2006). "Do Molecular Clocks Run at All? A Critique of Molecular Systematics". Biological Theory 1 (4): 357–371. doi:10.1162/biot.2006.1.4.357. Lay summary – Science Daily. 
  15. ^ Drummond, A.J., Ho, S.Y.W., Phillips, M.J. and Rambaut A. (2006). "Relaxed Phylogenetics and Dating with Confidence". PLoS Biology 4 (5): e88. doi:10.1371/journal.pbio.0040088. PMC 1395354. PMID 16683862. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1395354. 
  16. ^ Ho SYW, Phillips MJ, Cooper A, Drummond AJ (2005). "Time dependency of molecular rate estimates and systematic overestimation of recent divergence times". Molecular Biology & Evolution 22 (7): 1561–1568. doi:10.1093/molbev/msi145. PMID 15814826. 
  17. ^ Peterson GI, Masel J (2009). "Quantitative Prediction of Molecular Clock and Ka/Ks at Short Timescales". Molecular Biology & Evolution 26 (11): 2595–2603. doi:10.1093/molbev/msp175. PMC 2912466. PMID 19661199. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2912466. 

Further reading

External links


Wikimedia Foundation. 2010.

Игры ⚽ Поможем написать курсовую

Look at other dictionaries:

  • molecular clock — n a measure of evolutionary change over time at the molecular level that is based on the theory that specific DNA sequences or the proteins they encode spontaneously mutate at constant rates and that is used chiefly for estimating how long ago… …   Medical dictionary

  • molecular clock — molekulinis laikrodis statusas T sritis Standartizacija ir metrologija apibrėžtis Laikrodis, kuriame laiko masteliui sudaryti naudojami molekulių virpesiai. atitikmenys: angl. molecular clock vok. molekulare Uhr, f rus. молекулярные часы, m pranc …   Penkiakalbis aiškinamasis metrologijos terminų žodynas

  • molecular clock — molekulinis laikrodis statusas T sritis fizika atitikmenys: angl. molecular clock vok. molekulare Uhr, f rus. молекулярные часы pranc. horloge moléculaire, f …   Fizikos terminų žodynas

  • molecular clock — noun : a measure of evolutionary change over time at the molecular level that is based on the theory that specific DNA sequences or the proteins they encode spontaneously mutate at constant rates and that is used chiefly for estimating how long… …   Useful english dictionary

  • molecular clock — This term has two separate uses. In one sense it means the rate of fixation of mutations in DNA and thus times the rate of genetic diversification. In the second sense it means a biological system capable of maintaining a timing rhythm or pulse.… …   Dictionary of molecular biology

  • molecular clock — the changes in the amino acid sequences of proteins that take place during evolution and speciation, and from which the dates of branchings of taxonomic groups can be deduced. * * * …   Universalium

  • Molecular phylogenetics — (pronounced /məˈlɛkjʊlər faɪlɵdʒɪˈnɛtɪks/) is the analysis of hereditary molecular differences, mainly in DNA sequences, to gain information on an organism s evolutionary relationships. The result of a molecular phylogenetic analysis is… …   Wikipedia

  • Molecular anthropology — is a field of anthropology in which molecular analysis is used to determine evolutionary links between ancient and modern human populations, as well as between contemporary species. Generally, comparisons are made between sequence, either DNA or… …   Wikipedia

  • Molecular evolution — Part of a series on Evolutionary Biology …   Wikipedia

  • CLOCK — For other uses, see Clock (disambiguation). Clock homolog (mouse) Identifiers Symbols CLOCK; KAT13D; KIAA0334; bHLHe8 External IDs …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”