Literature DB >> 1901091

Uniformity in the nonsynonymous substitution rates of embryonic beta-globin genes of several vertebrate species.

S G Shapiro1.   

Abstract

The nucleotide substitution rate in structural portions of the embryonic beta-globin genes of placental mammals is lower than that for the adult beta-globin genes. This difference occurs entirely within the class of substitutions that result in nonsynonymous (replacement) differences between these genes, and therefore represents a constraint on the structure of the mammalian embryonic beta-globin proteins relative to the adult proteins (Shapiro et al. 1983; Hardison 1984). A similar effect has also been observed in marsupial mammals (Koop and Goodman 1988). In an effort to determine whether the observed rates are evidence of a uniform degree of selective constraint on the embryonic beta-globin genes, analyses were performed that compared replacement substitution rates. The analyses reveal that embryonic beta-globin genes appear to have been fixing replacement substitutions at nearly the same average rate not only in placental and marsupial mammals but in avian and amphibian species as well. In contrast, the adult beta-globin genes from these organisms appear to have a more variable rate of replacement substitution with an especially low rate for birds. In the chicken (Gallus gallus), the adult beta-globin gene replacement substitution rate appears to be lower than the embryonic replacement substitution rate.

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Year:  1991        PMID: 1901091     DOI: 10.1007/bf02515384

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


  29 in total

1.  Variances of the average numbers of nucleotide substitutions within and between populations.

Authors:  M Nei; L Jin
Journal:  Mol Biol Evol       Date:  1989-05       Impact factor: 16.240

2.  The evolution and sequence comparison of two recently diverged mouse chromosomal beta--globin genes.

Authors:  D A Konkel; J V Maizel; P Leder
Journal:  Cell       Date:  1979-11       Impact factor: 41.582

3.  Natural selection and the molecular clock.

Authors:  J H Gillespie
Journal:  Mol Biol Evol       Date:  1986-03       Impact factor: 16.240

4.  Structure and evolution of goat gamma-, beta C- and beta A-globin genes: three developmentally regulated genes contain inserted elements.

Authors:  E A Schon; M L Cleary; J R Haynes; J B Lingrel
Journal:  Cell       Date:  1981-12       Impact factor: 41.582

5.  The sequence of a mouse embryonic beta-globin gene. Evolution of the gene and its signal region.

Authors:  J N Hansen; D A Konkel; P Leder
Journal:  J Biol Chem       Date:  1982-01-25       Impact factor: 5.157

6.  The nucleotide sequence of rabbit embryonic globin gene beta 3.

Authors:  R C Hardison
Journal:  J Biol Chem       Date:  1981-11-25       Impact factor: 5.157

7.  Analysis of the adult chicken beta-globin gene. Nucleotide sequence of the locus, microheterogeneity at the 5'-end of beta-globin mRNA, and aberrant nuclear RNA species.

Authors:  M Dolan; J B Dodgson; J D Engel
Journal:  J Biol Chem       Date:  1983-03-25       Impact factor: 5.157

8.  Molecular evolution of myoglobin and the fossil record: a phylogenetic synthesis.

Authors:  A E Romero-Herrera; H Lehmann; K A Joysey; A E Friday
Journal:  Nature       Date:  1973-12-14       Impact factor: 49.962

9.  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

10.  The complete nucleotide sequence of the major adult beta globin gene of Xenopus laevis.

Authors:  R K Patient; R Harris; M E Walmsley; J G Williams
Journal:  J Biol Chem       Date:  1983-07-25       Impact factor: 5.157

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  3 in total

1.  Error in estimation of rate and time inferred from the early amniote fossil record and avian molecular clocks.

Authors:  Marcel van Tuinen; Elizabeth A Hadly
Journal:  J Mol Evol       Date:  2004-08       Impact factor: 2.395

2.  The evolutionary relationship of avian and mammalian myosin heavy-chain genes.

Authors:  L A Moore; W E Tidyman; M J Arrizubieta; E Bandman
Journal:  J Mol Evol       Date:  1993-01       Impact factor: 2.395

3.  Genomic organization and differential signature of positive selection in the alpha and beta globin gene clusters in two cetacean species.

Authors:  Mariana F Nery; José Ignacio Arroyo; Juan C Opazo
Journal:  Genome Biol Evol       Date:  2013       Impact factor: 3.416

  3 in total

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