Masatoshi Nei

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Masatoshi Nei
Masatoshi Nei - 2013.jpg
Born January 2, 1931
Miyazaki Prefecture, Japan
Fields molecular evolution
molecular phylogenetics
Institutions Pennsylvania State University
Alma mater University of Miyazaki(1953)
Kyoto University
Known for statistical theories of molecular evolution and development of the theory of mutation-driven evolution
Notable awards Member, National Academy of Sciences (1997)
International Prize for Biology (2002)
Thomas Hunt Morgan Medal (2006)
Kyoto Prize (2013)

Masatoshi Nei (根井正利 Nei Masatoshi?) is Evan Pugh Professor of Biology at Pennsylvania State University and Director of the Institute of Molecular Evolutionary Genetics since 1990. He was born in 1931 in Miyazaki Prefecture, on Kyūshū Island, Japan. He was associate professor and professor of biology at Brown University from 1969 to 1972 and professor of population genetics at the Center for Demographic and Population Genetics, University of Texas at Houston, from 1972 to 1990. He is a theoretical population geneticist and evolutionary biologist. Acting alone or working with his students, he has continuously developed new statistical theories of molecular evolution taking into account frontier knowledge of molecular biology. He has also developed several new concepts of evolutionary theory and proposed the theory of mutation-driven evolution.

Work in population genetics[edit]

Theoretical studies[edit]

He is the first to show mathematically that in the presence of gene interaction natural selection always tends to enhance the linkage intensity between genetic loci or maintain the same linkage relationship.[1] He then observed that the average recombination value per genome is generally lower in higher organisms than in lower organisms and attributed this observation to his theory of linkage modification.[2] Recent molecular data indicate that many sets of interacting genes such as Hox genes, immunoglobulin genes, and histone genes have often existed as gene clusters for a long evolutionary time. This observation can also be explained by his theory of linkage modification. He also showed that, unlike R. A. Fisher’s argument, deleterious mutations can accumulate rather quickly on the Y chromosome or duplicate genes in finite populations.[3][4] In 1969, considering the rates of amino acid substitution, gene duplication, and gene inactivation, he predicted that higher organisms contain a large number of duplicate genes and nonfunctional genes (now called pseudogenes).[5] This prediction was shown to be correct when many multigene families and pseudogenes were discovered in the 1980s and 1990s. His notable contribution in the early 1970s is the proposal of a new measure of genetic distance (Nei’s distance) between populations and its use for studying evolutionary relationships of populations or closely related species.[6] He later developed another distance measure called DA, which is appropriate for finding the topology of a phylogenetic tree of populations.[7] He also developed statistics of measuring the extent of population differentiation for any types of mating system using GST measure.[8] In 1975, he and collaborators presented a mathematical formulation of population bottleneck effects and clarified the genetic meaning of bottleneck effects.[9] In 1979, he proposed a statistical measure called nucleotide diversity,[10] which is now widely used for measuring the extent of nucleotide polymorphism. He also developed several different models of speciation and concluded that the reproductive isolation between species occurs as a passive process of accumulation of interspecific incompatibility mutations [11][12]

Protein polymorphism and neutral theory[edit]

In the early 1960s and 1970s, there was a great controversy over the mechanism of protein evolution and the maintenance of protein polymorphism. Nei and his collaborators developed various statistical methods for testing the neutral theory of evolution by using polymorphism data. Their analysis of the allele frequency distribution, the relationship between average heterozygosity and protein divergence between species, etc., showed that a large portion of protein polymorphism can be explained by neutral theory.[13] [14] The only exception was the major histocompatibility complex (MHC) loci, which show an extraordinarily high degree of polymorphism. For these reasons, he accepted the neutral theory of evolution.[14][15]

Human evolution[edit]

Using his genetic distance theory, he and A. K. Roychoudhury showed that the genetic variation between Europeans, Asians, and Africans is only about 11 percent of the total genetic variation of the human population. They then estimated that Europeans and Asians diverged about 55,000 years ago and these two populations diverged from Africans about 115,000 years ago.[16][17] This conclusion was supported by many later studies using larger numbers of genes and populations, and the estimates appear to be still roughly correct. This finding represents the first indication of the out-of-Africa theory of human origins.

Molecular phylogenetics[edit]

Around 1980, Nei and his students initiated a study of inference of phylogenetic trees based on distance data. In 1985 they developed a statistical method for testing the accuracy of a phylogenetic tree by examining the statistical significance of interior branch lengths. They then developed the neighbor-joining and minimum-evolution methods of tree inference.[18] [19] At present, the neighbor-joining method is most widely used in molecular phylogenetics, though some theoreticians advocate the likelihood and the Bayesian methods.[20] They also developed statistical methods for estimating evolutionary times from molecular phylogenies. In collaboration with Sudhir Kumar and Koichiro Tamura, he developed a widely used computer program package for phylogenetic analysis called MEGA.[21]

MHC loci and positive Darwinian selection[edit]

Nei’s group invented a simple statistical method for detecting positive Darwinian selection by comparing the numbers of synonymous nucleotide substitutions and nonsynonymous nucleotide substitutions. .[22] Applying this method, they showed that the exceptionally high degree of sequence polymorphism at MHC loci is caused by overdominant selection.[23] Although various statistical methods for this test have been developed later, their original methods are still widely used.[24]

New evolutionary concepts[edit]

Nei and his students studied the evolutionary patterns of a large number of multigene families and showed that they generally evolve following the model of a birth-and-death process.[25] In some gene families this process is very fast and caused by random events of gene duplication and gene deletion and generates genomic drift of gene copy number. Nei has long maintained the view that the driving force of evolution is mutation including any types of DNA changes (nucleotide changes, chromosomal changes, and genome duplication) and natural selection is merely a force eliminating less fit genotypes (theory of mutation-driven evolution).[14][24] He conducted statistical analyses of evolution of genes controlling phenotypic characters such as immunity and olfactory reception and obtained evidence supporting this theory.[24]

New journal, new society, and students[edit]

He founded the journal Molecular Biology and Evolution in 1983 and the Society for Molecular Biology and Evolution in 1993, together with Walter M. Fitch. He also trained many graduate students and postdoctorals who later became leading figures in molecular evolutionary biology including Margaret Kidwell, Wen-Hsiung Li, Ranajit Chakraborty, Shozo Yokoyama, Aravinda Chakravarti, Dan Graur, Fumio Tajima, Naruya Saitou, Chung-I Wu, Naoyuki Takahata, Takashi Gojobori, Pekka Pamilo, Austin Hughes, Andrey Rzhetsky, Jianzhi (George) Zhang, and Sudhir Kumar.

Recognition[edit]

See also[edit]

References[edit]

  1. ^ Nei, Masatoshi (1967). "Modification of linkage intensity by natural selection". Genetics 57 (3): 625–641. PMC 1211753. PMID 5583732. 
  2. ^ Nei, Masatoshi (1968). "Evolutionary change of linkage intensity". Nature 218 (5147): 1160–1161. doi:10.1038/2181160a0. PMID 5656638. 
  3. ^ Nei, M. (1970) Accumulation of nonfunctional genes on sheltered chromosomes. Am. Nat. 104:311-322
  4. ^ Nei, M. and A. K. Roychoudhury (1973) Probability of fixation of nonfunctional genes at duplicate loci. Am. Nat. 107:362-372
  5. ^ Nei, M. (1969) Gene duplication and nucleotide substitution in evolution. Nature 221:40-42
  6. ^ Nei, M. (1972) Genetic distance between populations. Am. Nat. 106:283-292
  7. ^ Nei, M., F. Tajima, & Y. Tateno (1983) Accuracy of estimated phylogenetic trees from molecular data. II. Gene frequency data. J. Mol. Evol. 19:153-170.
  8. ^ Nei, M. (1973) Analysis of gene diversity in subdivided populations. Proc. Natl. Acad. Sci. USA 70:3321-3323.
  9. ^ Nei, M., T. Maruyama and R. Chakraborty (1975) The bottleneck effect and genetic variability in populations. Evolution 29:1-10
  10. ^ Nei, Masatoshi; Li, Wen-Hsiung (October 1979). "Mathematical model for studying genetic variation in terms of restriction endonucleases". Proc. Natl. Acad. Sci. USA 76 (10):5269-5273. PMC 413122. PMID 291943,
  11. ^ Nei, M. T. Maruyama, and C. I. Wu (1983) Models of evolution of reproductive isolation. Genetics 103:557-579.
  12. ^ Nei, M., and M. Nozawa (2011) Roles of Mutation and Selection in Speciation: From Hugo de Vries to the modern genomic era. Genome Biol Evol 3:812-829.
  13. ^ Nei, M. (1983) Genetic polymorphism and the role of mutation in evolution (P. K. Koehn and M. Nei, eds.) Evolution of Genes and Proteins. Sinauer Assoc., Sunderland, MA, pp. 165-190.
  14. ^ a b c Nei, M. (1987) Molecular Evolutionary Genetics. Columbia University Press, New York.
  15. ^ Li, W. H., T. Gojobori, and M. Nei (1981) Pseudogenes as a paradigm of neutral evolution. Nature 292:237-239.
  16. ^ Nei, M. and A. K. Roychoudhury (1974) Genic variation within and between the three major races of man, Caucasoids, Negroids, and Mongoloids. Am. J. Hum. Genet. 26:421-443.
  17. ^ Nei, M. and A. K. Roychoudhury (1982) Genetic relationship and evolution of human races. Evol. Biol. 14:1-59.
  18. ^ Saitou, N. and M. Nei (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol. Biol. Evol. 4:406-425.
  19. ^ Rzhetsky, A. and M. Nei (1993) Theoretical foundation of the minimum-evolution method of phylogenetic inference. Mol. Biol. Evol. 10:1073-1095.
  20. ^ Nei, M., and S. Kumar (2000) Molecular Evolution and Phylogenetics. Oxford University Press, Oxford.
  21. ^ Kumar, S., K. Tamura, and M. Nei (1993) MEGA: Molecular Evolutionary Genetics Analysis. Ver. 1.02, The Pennsylvania State University, University Park, PA.
  22. ^ Nei, M. and T. Gojobori (1986) Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions. Mol. Biol. Evol. 3:418-426.
  23. ^ Hughes, A. L. and M. Nei (1988) Pattern of nucleotide substitution at major histocompatibility complex class I loci reveals overdominant selection. Nature 335:167-170.
  24. ^ a b c Nei, M. (2013) Mutation-Driven Evolution. Oxford University Press, Oxford.
  25. ^ Nei, M. and A. P. Rooney (2005) Concerted and birth-and-death evolution of multigene families.

Books[edit]

  • Nei, M.(2013) Mutation-Driven Evolution. Oxford University Press, Oxford.
  • Nei, M., and S. Kumar (2000) Molecular Evolution and Phylogenetics. Oxford University Press, Oxford.
  • Roychoudhury, A. K., and M. Nei (1988) Human Polymorphic Genes: World Distribution. Oxford University Press, Oxford and New York.
  • Nei, M. (1987) Molecular Evolutionary Genetics. Columbia University Press, New York.
  • Nei, M., and R. K. Koehn (eds). (1983) Evolution of Genes and Proteins. Sinauer Assoc., Sunderland, MA.
  • Nei, M. (1975) Molecular Population Genetics and Evolution. North-Holland, Amsterdam and New York.

External links[edit]