Literature DB >> 9767692

Phylogenetic analysis of reptilian hemoglobins: trees, rates, and divergences.

T A Gorr1, B K Mable, T Kleinschmidt.   

Abstract

Phylogenetic relationships among reptiles were examined using previously published and newly determined hemoglobin sequences. Trees reconstructed from these sequences using maximum-parsimony, neighbor-joining, and maximum-likelihood algorithms were compared with a phylogenetic tree of Amniota, which was assembled on the basis of published morphological data. All analyses differentiated alpha chains into alphaA and alphaD types, which are present in all reptiles except crocodiles, where only alphaA chains are expressed. The occurrence of the alphaD chain in squamates (lizards and snakes only in this study) appears to be a general characteristic of these species. Lizards and snakes also express two types of beta chains (betaI and betaII), while only one type of beta chain is present in birds and crocodiles. Reconstructed hemoglobin trees for both alpha and beta sequences did not yield the monophyletic Archosauria (i.e., crocodilians + birds) and Lepidosauria (i.e., Sphenodon + squamates) groups defined by the morphology tree. This discrepancy, as well as some other poorly resolved nodes, might be due to substantial heterogeneity in evolutionary rates among single hemoglobin lineages. Estimation of branch lengths based on uncorrected amino acid substitutions and on distances corrected for multiple substitutions (PAM distances) revealed that relative rates for squamate alphaA and alphaD chains and crocodilian beta chains are at least twice as high as those of the rest of the chains considered. In contrast to these rate inequalities between reptilian orders, little variation was found within squamates, which allowed determination of absolute evolutionary rates for this subset of hemoglobins. Rate estimates for hemoglobins of lizards and snakes yielded 1.7 (alphaA) and 3.3 (beta) million years/PAM when calibrated with published divergence time vs. PAM distance correlates for several speciation events within snakes and for the squamate left and right arrow sphenodontid split. This suggests that hemoglobin chains of squamate reptiles evolved approximately 3.5 (alphaA) or approximately 1.7 times (beta) faster than their mammalian equivalents. These data also were used to obtain a first estimate of some intrasquamate divergence times.

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Year:  1998        PMID: 9767692     DOI: 10.1007/pl00006404

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


  11 in total

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3.  The Primary Structure of β(I)-Chain of Hemoglobin from Snake Sindhi Krait (Bungarus sindanus sindanus).

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4.  Oxygenation properties and isoform diversity of snake hemoglobins.

Authors:  Jay F Storz; Chandrasekhar Natarajan; Hideaki Moriyama; Federico G Hoffmann; Tobias Wang; Angela Fago; Hans Malte; Johannes Overgaard; Roy E Weber
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2015-09-09       Impact factor: 3.619

5.  Globin gene structure in a reptile supports the transpositional model for amniote α- and β-globin gene evolution.

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7.  Lineage-specific patterns of functional diversification in the alpha- and beta-globin gene families of tetrapod vertebrates.

Authors:  Federico G Hoffmann; Jay F Storz; Thomas A Gorr; Juan C Opazo
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8.  Lack of conventional oxygen-linked proton and anion binding sites does not impair allosteric regulation of oxygen binding in dwarf caiman hemoglobin.

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9.  Integration of molecules and new fossils supports a Triassic origin for Lepidosauria (lizards, snakes, and tuatara).

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10.  Gene Turnover and Diversification of the α- and β-Globin Gene Families in Sauropsid Vertebrates.

Authors:  Federico G Hoffmann; Michael W Vandewege; Jay F Storz; Juan C Opazo
Journal:  Genome Biol Evol       Date:  2018-01-01       Impact factor: 3.416

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