Abstract
Molecular evolution is an expansive and highly interdisciplinary field of research that investigates the evolution of biological molecules and molecular phenomena over time. A notable feature of the field is its ability to embrace and adapt to novel molecular methods, technology, and data while developing and applying a rigorous theoretical framework of population genetics to data interpretation. In the early days of molecular biology, as protein and DNA sequences began to accumulate, molecular evolutionary analyses contributed to the development of several fundamental concepts that remain impactful even after several decades. From preliminary comparisons of protein sequences from distantly related species emerged the idea of a constant molecular clock. In turn, this idea became one of the main inspirations for the neutral theory of molecular evolution, which provides the basis for widely used statistical approaches to test selection using molecular data, including genome sequences. The nearly neutral theory emphasizes that the evolutionary dynamics of many mutations are governed by genetic drift because their effects on fitness are borderline neutral, and this theory can explain many broad patterns of molecular evolution. As the field of molecular evolution embraces the so-called ‘omics’ era, these foundational ideas continue to provide guiding principles.
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References
Akashi H, Osada N, Ohta T (2012) Weak selection and protein evolution. Genetics 192:15–31
Bird A (1980) DNA methylation and the frequency of CpG in animal DNA. Nucleic Acids Res 8:1499–1504
Dickerson RE (1971) The structure of cytochrome c and the rates of molecular evolution. J Mol Evol 1:26–45
Dietrich MR (1998) Paradox and persuasion: negotiating the place of molecular evolution within evolutionary biology. J Hist Biol 31:85–111
Doolittle RF, Blombäck B (1964) Amino-acid sequence investigations of fibrinopeptides from various mammals: evolutionary implications. Nature 202:147–152
Goodman M (1961) The role of immunologic differences in the phyletic development of human behavior. Hum Biol 33:131–162
Goodman M (1962) Evolution of the immunologic species specificity of human serum proteins. Hum Biol 34:104–150
Goodman M (1963) Man’s place in the phylogeny of the primates as reflected in serum proteins. In: Washburn SL (ed) Classification and human evolution. Aldine Press, Chicago, IL, pp 204–234
Haldane JBS (1947) The mutation rate of the gene for hemophilia, and its segregation ratios in males and females. Ann Eugenics 13:262–272
Haldane JBS (1957) The cost of natural selection. J Genet 55:511–524
Hubby JL, Lewontin RC (1966) A molecular approach to the study of genic heterozygosity in natural populations. I. The number of alleles at different loci in Drosophila pseudoobscura. Genetics 54:577–594
Hudson RR, Kreitman M, Aguadé M (1987) A test of neutral molecular evolution based on nucleotide data. Genetics 116:153–159
Kim S-H, Elango N, Warden CW, Vigoda E, Yi S (2006) Heterogeneous genomic molecular clocks in primates. PLOS Genet 2:e163
Kimura M (1960) Optimum mutation rate and degree of dominance as determined by the principle of minimum genetic load. J Genet 57:21–34
Kimura M (1968) Evolutionary rate at the molecular level. Nature 217:624–626
Kimura M (1977) Preponderance of synonymous changes as evidence for the neutral theory of molecular evolution. Nature 267:275–276
Kimura M (1983) The neutral theory of molecular evolution. Cambridge University Press, Cambridge
Kimura M, Ohta T (1971a) On the rate of molecular evolution. J Mol Evol 1:1–17
Kimura M, Ohta T (1971b) Protein polymorphism as a phase of molecular evolution. Nature 229:467–469
King JL, Jukes T (1969) Non-Darwinian evolution. Science 164:788–798
Kohne C (1970) Evolution of higher-organism DNA. Q Rev Biophys 3:327–375
Kosiol C, Vinar T, da Fonseca RR, Hubisz MJ, Bustamante CD, Nielsen R, Siepel A (2008) Patterns of positive selection in six mammalian genomes. PLOS Genet 4:e1000144
Laird CD, McConaughy BL, McCarthy BJ (1969) Rate of fixation of nucleotide substitutions in evolution. Nature 224:149–154
Lewontin RC, Hubby JL (1966) A molecular approach to the study of genetic heterozygosity in natural populations. II. Amount of variation and degree of heterozygosity in natural populations of Drosophila pseudoobscura. Genetics 54:595–609
Li W-H, Gojobori T, Nei M (1981) Pseudogenes as a paradigm of neutral evolution. Nature 292:237–239
Lynch M (2007) The origins of genome architecture. Sinauer Associates, Sunderland, MA
Lynch M, Conery JS (2003) The origins of genome complexity. Science 302:1401–1404
Lynch M, Ackerman MS, Gout J-F, Long H, Sung W, Thomas WK, Foster PL (2016) Genetic drift, selection and the evolution of the mutation rate. Nat Rev Genet 17:704–714
Margoliash E (1963) Primary structure and evolution of cytochrome c. Proc Natl Acad Sci USA 50:672–679
Margulies EH, Blanchette M, Comparative Sequencing Program NISC, Haussler D, Green ED (2003) Identification and characterization of multi-species conserved sequences. Genome Res 13:2507–2518
McDonald JH, Kreitman M (1991) Adaptive protein evolution at the Adh locus in Drosophila. Nature 351:652–654
Moorjani P, Amorim CEG, Arndt PF, Przeworski M (2016) Variation in the molecular clock of primates. Proc Natl Acad Sci USA 113:10607–10612
Morgan GJ (1998) Emile Zuckerkandl, Linus Pauling, and the molecular evolutionary clock, 1959–1965. J Hist Biol 31:155–178
Muller HJ (1954) The nature of the genetic effects produced by radiation. In: Hollaender A (ed) Radiation biology. McGraw-Hill, New York, pp 351–473
Nei M (2005) Selectionism and neutralism in molecular evolution. Mol Biol Evol 22:2318–2342
Nuttall GHF (1904) Blood immunity and blood relationship. Cambridge University Press, Cambridge
Ohta T (1972a) Evolutionary rate of cistrons and DNA divergence. J Mol Evol 1:150–157
Ohta T (1972b) Population size and rate of evolution. J Mol Evol 1:305–314
Ohta T (1973) Slightly deleterious mutant substitutions in evolution. Nature 246:96–98
Ohta T (1974) Mutational pressure as the main cause of molecular evolution and polymorphism. Nature 252:351–354
Ohta T (1995) Synonymous and nonsynonymous substitutions in mammalian genes and the nearly neutral theory. J Mol Evol 40:56–63
Ohta T (2002) Near-neutrality in evolution of genes and gene regulation. Proc Natl Acad Sci USA 99:16134–16137
Ohta T (2011) Near-neutrality, robustness, and epigenetics. Genome Biol Evol 3:1034–1038
Ohta T, Kimura M (1971) On the constancy of the evolutionary rate of cistrons. J Mol Evol 1:18–25
Rhesus Macaque Genome Sequencing and Analysis Consortium (2007) Evolutionary and biomedical insights from the rhesus macaque genome. Science 316:222–234
Sarich VM, Wilson AC (1967) Immunological time scale for hominid evolution. Science 158:1200–1203
Sung W, Ackerman MS, Miller SF, Doak TG, Lynch M (2012) Drift-barrier hypothesis and mutation-rate evolution. Proc Natl Acad Sci USA 109:18488–18492
Suzuki MM, Bird A (2008) DNA methylation landscapes: provocative insights from epigenomics. Nat Rev Genet 9:465–476
Tajima F (1989) Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123:585–595
Takahata N (2007) Molecular clock: an anti-neo-Darwinian legacy. Genetics 176:1–6
Thomas JA, Welch JJ, Lanfear R, Bromham L (2010) A generation time effect on the rate of molecular evolution in invertebrates. Mol Biol Evol 27:1173–1180
Tsantes C, Steiper ME (2009) Age at first reproduction explains rate variation in the strepsirrhine molecular clock. Proc Natl Acad Sci USA 106:18165–18170
Vandiver AR, Idrizi A, Rizzardi L, Feinberg AP, Hansen KD (2015) DNA methylation is stable during replication and cell cycle arrest. Sci Rep 5:17911
Welch JJ, Bininda-emonds ORP, Bromham L (2008) Correlates of substitution rate variation in mammalian protein-coding sequences. BMC Evol Biol 8:53
Wilson AC, Sarich VM (1969) A molecular time scale for human evolution. Proc Natl Acad Sci USA 63:1088–1093
Woolfe A, Goodson M, Goode DK, Snell P, McEwen GK, Vavouri T, Smith SF, North P, Callaway H, Kelly K, Walter K, Abnizova I, Gilks W, Edwards YJK, Cooke JE, Elgar G (2004) Highly conserved non-coding sequences are associated with vertebrate development. PLOS Biol 3:e7
Wu C-I, Li W-H (1985) Evidence for higher rates of nucleotide substitution in rodents than in man. Proc Natl Acad Sci USA 82:1741–1745
Yi S (2012) Birds do it, bees do it, worms and ciliates do it too: DNA methylation from unexpected corners of the tree of life. Genome Biol 13:174
Yi S, Ellsworth DL, Li WH (2002) Slow molecular clocks in Old World monkeys, apes, and humans. Mol Biol Evol 19:2191–2198
Zuckerkandl E, Pauling L (1962) Molecular disease, evolution, and genic heterogeneity. In: Kasha M, Pullman B (eds) Horizons in biochemistry. Academic, New York, pp 189–225
Zuckerkandl E, Pauling L (1965) Evolutionary divergence and convergence in proteins. In: Bryson V, Vogel HJ (eds) Evolving genes and proteins. Academic, New York, pp 97–166
Zuckerkandl E, Jones RT, Pauling L (1960) A comparison of animal hemoglobin by tryptic peptide pattern analysis. Proc Natl Acad Sci USA 46:1349–1360
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Yi, S.V. (2020). Molecular Evolution: A Brief Introduction. In: Ho, S.Y.W. (eds) The Molecular Evolutionary Clock. Springer, Cham. https://doi.org/10.1007/978-3-030-60181-2_2
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DOI: https://doi.org/10.1007/978-3-030-60181-2_2
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