Literature DB >> 7161811

Accepted mutations in a gene family: evolutionary diversification of duplicated DNA.

C W Jones, F C Kafatos.   

Abstract

We report and compare the DNA sequences of 14 silkmoth (Antheraea polyphemus) chorion genes, derived from either cDNA or chromosomal DNA clones. Seven of these genes are members of the A multigene family, and seven are members of the B family. Where available, the previously reported (Jones and Kafatos 1980) intronic and extragenic flanking DNA sequences are also considered. Closely related sequences are compared, revealing the types of spontaneous mutations that were fixed during paralogous evolution. Segmental mutations (i.e. mutations other than substitutions) are nearly always interpretable as small duplications or deletions, related to small direct repeats. Segmental mutations are strongly constrained in the coding regions, although they do occur. Nucleotide substitutions also appear to be under selective constraints: relatively few substitutions leading to amino acid replacements are accepted, silent substitutions leading to some codons (especially purine-terminated ones) are disfavored, and different compositional biases are maintained in different parts of the sequences. Other sequence differences can be interpreted as indicative of neutral drift, including most differences in non-coding regions and most T/C transitions in third-base positions. In the non-coding regions, which are thought to be only loosely constrained by selection, transitions are observed more frequently than might be expected: they account for 52% of all substitutions, and they appear to be favored two to threefold over transversions when allowance is made for the skewed base composition of these regions.

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Year:  1982        PMID: 7161811     DOI: 10.1007/bf02100227

Source DB:  PubMed          Journal:  J Mol Evol        ISSN: 0022-2844            Impact factor:   2.395


  31 in total

1.  Complementary base pairing and the origin of substitution mutations.

Authors:  M D Topal; J R Fresco
Journal:  Nature       Date:  1976-09-23       Impact factor: 49.962

2.  Genetic studies of the lac repressor. VII. On the molecular nature of spontaneous hotspots in the lacI gene of Escherichia coli.

Authors:  P J Farabaugh; U Schmeissner; M Hofer; J H Miller
Journal:  J Mol Biol       Date:  1978-12-25       Impact factor: 5.469

3.  Protein polymorphism as a phase of molecular evolution.

Authors:  M Kimura; T Ohta
Journal:  Nature       Date:  1971-02-12       Impact factor: 49.962

4.  Structure, organization and evolution of developmentally regulated chorion genes in a silkmoth.

Authors:  C W Jones; F C Kafatos
Journal:  Cell       Date:  1980-12       Impact factor: 41.582

5.  The structure and evolution of the human beta-globin gene family.

Authors:  A Efstratiadis; J W Posakony; T Maniatis; R M Lawn; C O'Connell; R A Spritz; J K DeRiel; B G Forget; S M Weissman; J L Slightom; A E Blechl; O Smithies; F E Baralle; C C Shoulders; N J Proudfoot
Journal:  Cell       Date:  1980-10       Impact factor: 41.582

6.  Some rules in the ordering of nucleotides in the DNA.

Authors:  R Nussinov
Journal:  Nucleic Acids Res       Date:  1980-10-10       Impact factor: 16.971

7.  The evolution of genes: the chicken preproinsulin gene.

Authors:  F Perler; A Efstratiadis; P Lomedico; W Gilbert; R Kolodner; J Dodgson
Journal:  Cell       Date:  1980-06       Impact factor: 41.582

8.  Complete nucleotide sequence of bacteriophage MS2 RNA: primary and secondary structure of the replicase gene.

Authors:  W Fiers; R Contreras; F Duerinck; G Haegeman; D Iserentant; J Merregaert; W Min Jou; F Molemans; A Raeymaekers; A Van den Berghe; G Volckaert; M Ysebaert
Journal:  Nature       Date:  1976-04-08       Impact factor: 49.962

9.  Mitochondrial DNA sequences of primates: tempo and mode of evolution.

Authors:  W M Brown; E M Prager; A Wang; A C Wilson
Journal:  J Mol Evol       Date:  1982       Impact factor: 2.395

10.  Use of a cDNA library for studies on evolution and developmental expression of the chorion multigene families.

Authors:  G K Sim; F C Kafatos; C W Jones; M D Koehler; A Efstratiadis; T Maniatis
Journal:  Cell       Date:  1979-12       Impact factor: 41.582

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  39 in total

1.  Melamine deaminase and atrazine chlorohydrolase: 98 percent identical but functionally different.

Authors:  J L Seffernick; M L de Souza; M J Sadowsky; L P Wackett
Journal:  J Bacteriol       Date:  2001-04       Impact factor: 3.490

Review 2.  Evolutionary consequences of nonrandom damage and repair of chromatin domains.

Authors:  T Boulikas
Journal:  J Mol Evol       Date:  1992-08       Impact factor: 2.395

3.  Nonuniform evolution of duplicated, developmentally controlled chorion genes in a silkmoth.

Authors:  S G Tsitilou; F C Kafatos
Journal:  J Mol Evol       Date:  1989-11       Impact factor: 2.395

4.  Temporal regulation in development: negative and positive cis regulators dictate the precise timing of expression of a Drosophila chorion gene.

Authors:  B D Mariani; J R Lingappa; F C Kafatos
Journal:  Proc Natl Acad Sci U S A       Date:  1988-05       Impact factor: 11.205

5.  Evolution of the IgA heavy chain gene in the genus Mus.

Authors:  B A Osborne; T E Golde; R L Schwartz; S Rudikoff
Journal:  Genetics       Date:  1988-08       Impact factor: 4.562

6.  Coding and potential regulatory sequences of a cluster of chorion genes in Drosophila melanogaster.

Authors:  Y C Wong; J Pustell; N Spoerel; F C Kafatos
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

7.  The legumin gene family: structure and evolutionary implications of Vicia faba B-type genes and pseudogenes.

Authors:  U Heim; R Schubert; H Bäumlein; U Wobus
Journal:  Plant Mol Biol       Date:  1989-12       Impact factor: 4.076

8.  Novel B family sequence from an early chorion cDNA library of Bombyx mori.

Authors:  R Lecanidou; T H Eickbush; G C Rodakis; F C Kafatos
Journal:  Proc Natl Acad Sci U S A       Date:  1983-04       Impact factor: 11.205

9.  Structural analysis of a rabbit immunoglobulin kappa 2 J-C locus reveals multiple deletions.

Authors:  L Emorine; E E Max
Journal:  Nucleic Acids Res       Date:  1983-12-20       Impact factor: 16.971

10.  Structure and evolution of a mouse tRNA gene cluster encoding tRNAAsp, tRNAGly and tRNAGlu and an unlinked, solitary gene encoding tRNAAsp.

Authors:  J E Looney; J D Harding
Journal:  Nucleic Acids Res       Date:  1983-12-20       Impact factor: 16.971

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