Literature DB >> 7815925

Molecular evolution at subzero temperatures: mitochondrial and nuclear phylogenies of fishes from Antarctica (suborder Notothenioidei), and the evolution of antifreeze glycopeptides.

L Bargelloni1, P A Ritchie, T Patarnello, B Battaglia, D M Lambert, A Meyer.   

Abstract

Most fishes of the perciform suborder Notothenioidei are endemic to the subzero marine waters of Antarctica. A number of remarkable physiological attributes allow them to inhabit this extreme environment; for example, the blood of almost all notothenioid species contains antifreeze glycopeptides. To establish a molecular phylogenetic hypothesis for these fishes, DNA sequences from two mitochondrial genes, portions of the 12S and 16S ribosomal genes (928 base pairs [bp]), were determined for 18 species. These belong to 15 genera in five families of the suborder. The DNA data suggest that two of these families are unnatural groups and consequently that the classification and phylogeny of this suborder is in need of revision. In terms of DNA variation, the Bovichtidae are a distantly related sister group to the other families of the suborder that includes the icefishes, the only vertebrates without hemoglobin. The fishes of the suborder (except the Bovichtidae) seem to have speciated rapidly, forming an adaptive radiation in the Antarctic waters. A phylogenetic analysis of published hemoglobin amino acid sequences for other notothenioid fishes supports these results from mtDNA. On the basis of molecular phylogeny, the evolution of antifreeze glycopeptides was studied. The age of the radiation of notothenioid fishes had been estimated to be at least 38 Mya. However, the level of mtDNA variation detected in notothenioid fishes appears to be too low to agree with this date of origin and might instead suggest a younger age (10-15 Mya). Alternatively, the low level of detected mtDNA variation would agree with the traditional old-age estimate if an extremely slow rate of mtDNA evolution is postulated for this group. This slow-rate hypothesis, if true, could be explained by decreased metabolic rates slowing down the tempo of molecular evolution.

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Year:  1994        PMID: 7815925     DOI: 10.1093/oxfordjournals.molbev.a040168

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


  17 in total

1.  Atypically low rate of cytochrome b evolution in the scleractinian coral genus Acropora.

Authors:  M J van Oppen; B L Willis; D J Miller
Journal:  Proc Biol Sci       Date:  1999-01-22       Impact factor: 5.349

2.  Structure and function of the Gondwanian hemoglobin of Pseudaphritis urvillii, a primitive notothenioid fish of temperate latitudes.

Authors:  Cinzia Verde; Barry D Howes; M Cristina De Rosa; Luca Raiola; Giulietta Smulevich; Richard Williams; Bruno Giardina; Elio Parisi; Guido Di Prisco
Journal:  Protein Sci       Date:  2004-08-31       Impact factor: 6.725

3.  Molecular evolution of hemoglobins of Antarctic fishes (Notothenioidei).

Authors:  W T Stam; J J Beintema; R D'Avino; M Tamburrini; G di Prisco
Journal:  J Mol Evol       Date:  1997-10       Impact factor: 2.395

4.  Origin of antifreeze protein genes: a cool tale in molecular evolution.

Authors:  J M Logsdon; W F Doolittle
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-15       Impact factor: 11.205

5.  Evolution of antifreeze glycoprotein gene from a trypsinogen gene in Antarctic notothenioid fish.

Authors:  L Chen; A L DeVries; C H Cheng
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-15       Impact factor: 11.205

6.  Convergent evolution of antifreeze glycoproteins in Antarctic notothenioid fish and Arctic cod.

Authors:  L Chen; A L DeVries; C H Cheng
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-15       Impact factor: 11.205

7.  Iterative Calibration: A Novel Approach for Calibrating the Molecular Clock Using Complex Geological Events.

Authors:  Tzitziki Loeza-Quintana; Sarah J Adamowicz
Journal:  J Mol Evol       Date:  2018-02-10       Impact factor: 2.395

8.  Variable expression of myoglobin among the hemoglobinless Antarctic icefishes.

Authors:  B D Sidell; M E Vayda; D J Small; T J Moylan; R L Londraville; M L Yuan; K J Rodnick; Z A Eppley; L Costello
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-01       Impact factor: 11.205

9.  The complete mitochondrial genome of rock carp Procypris rabaudi (Cypriniformes: Cyprinidae) and phylogenetic implications.

Authors:  Xiuyue Zhang; Bisong Yue; Wanxiang Jiang; Zhaobin Song
Journal:  Mol Biol Rep       Date:  2008-05-22       Impact factor: 2.316

10.  Antarctic fish hemoglobins: evidence for adaptive evolution at subzero temperature.

Authors:  L Bargelloni; S Marcato; T Patarnello
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-21       Impact factor: 11.205

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