Literature DB >> 2835574

Evolutionary change of restriction cleavage sites and phylogenetic inference for man and apes.

M Nei1, F Tajima.   

Abstract

A mathematical theory for the evolutionary change of restriction endonuclease cleavage sites is developed, and the probabilities of various types of restriction-site changes are evaluated. A computer simulation is also conducted to study properties of the evolutionary change of restriction sites. These studies indicate that parsimony methods of constructing phylogenetic trees often make erroneous inferences about evolutionary changes of restriction sites unless the number of nucleotide substitutions per site is less than 0.01 for all branches of the tree. This introduces a systematic error in estimating the number of mutational changes for each branch and, consequently, in constructing phylogenetic trees. Therefore, parsimony methods should be used only in cases where nucleotide sequences are closely related. Reexamination of Ferris et al.'s data on restriction-site differences of mitochondrial DNAs does not support Templeton's conclusions regarding the phylogenetic tree for man and apes and the molecular clock hypothesis. Templeton's claim that Nei and Li's method of estimating the number of nucleotide substitutions per site is seriously affected by parallel losses and loss-gains of restriction sites is also unsupported.

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Year:  1985        PMID: 2835574     DOI: 10.1093/oxfordjournals.molbev.a040345

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  12 in total

1.  Evolution of four human Y chromosomal unique sequences.

Authors:  R P Erickson
Journal:  J Mol Evol       Date:  1987       Impact factor: 2.395

2.  The number of nucleotides required to determine the branching order of three species, with special reference to the human-chimpanzee-gorilla divergence.

Authors:  N Saitou; M Nei
Journal:  J Mol Evol       Date:  1986       Impact factor: 2.395

3.  Evolutionary change of restriction sites under unequal rates of nucleotide substitution among the three positions of codons.

Authors:  W H Li
Journal:  J Mol Evol       Date:  1986       Impact factor: 2.395

4.  Correcting coalescent analyses for panel-based SNP ascertainment.

Authors:  James R McGill; Elizabeth A Walkup; Mary K Kuhner
Journal:  Genetics       Date:  2013-01-18       Impact factor: 4.562

5.  DNA hybridization evidence of hominoid phylogeny: results from an expanded data set.

Authors:  C G Sibley; J E Ahlquist
Journal:  J Mol Evol       Date:  1987       Impact factor: 2.395

6.  Tricky relatives: consecutive dichotomous speciation of gorilla, chimpanzee and hominids testified by immunological determinants.

Authors:  K Bauer; A Schreiber
Journal:  Naturwissenschaften       Date:  1995-11

7.  Parasite polymorphism and severe malaria in Dakar (Senegal): a West African urban area.

Authors:  Ndeye Sakha Bob; Bernard Marcel Diop; Francois Renaud; Laurence Marrama; Patrick Durand; Adama Tall; Boubacar Ka; Marie Therese Ekala; Christiane Bouchier; Odile Mercereau-Puijalon; Ronan Jambou
Journal:  PLoS One       Date:  2010-03-23       Impact factor: 3.240

8.  Man's place in Hominoidea as inferred from molecular clocks of DNA.

Authors:  M Hasegawa; H Kishino; T Yano
Journal:  J Mol Evol       Date:  1987       Impact factor: 2.395

9.  Genetic absolute dating based on microsatellites and the origin of modern humans.

Authors:  D B Goldstein; A Ruiz Linares; L L Cavalli-Sforza; M W Feldman
Journal:  Proc Natl Acad Sci U S A       Date:  1995-07-18       Impact factor: 11.205

10.  CoPAP: Coevolution of presence-absence patterns.

Authors:  Ofir Cohen; Haim Ashkenazy; Eli Levy Karin; David Burstein; Tal Pupko
Journal:  Nucleic Acids Res       Date:  2013-06-08       Impact factor: 16.971

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