Literature DB >> 1501250

Molecules, fossils, and the origin of tetrapods.

A Meyer1, S I Dolven.   

Abstract

Since the discovery of the coelacanth, Latimeria chalumnae, more than 50 years ago, paleontologists and comparative morphologists have debated whether coelacanths or lungfishes, two groups of lobe-finned fishes, are the closest living relatives of land vertebrates (Tetrapoda). Previously, Meyer and Wilson (1990) determined partial DNA sequences from two conservative mitochondrial genes and found support for a close relationship of lungfishes to tetrapods. We present additional DNA sequences from the 12S rRNA mitochondrial gene for three species of the two lineages of lungfishes that were not represented in the first study: Protopterus annectens and Protopterus aethiopicus from Africa and Neoceratodus forsteri (kindly provided by B. Hedges and L. Maxson) from Australia. This extended data set tends to group the two lepidosirenid lungfish lineages (Lepidosiren and Protopterus) with Neoceratodus as their sister group. All lungfishes seem to be more closely related to tetrapods than the coelacanth is. This result appears to rule out the possibility that the coelacanth lineage gave rise to land vertebrates. The common ancestor of lungfishes and tetrapods might have possessed multiple morphological traits that are shared by lungfishes and tetrapods [Meyer and Wilson (1990) listed 14 such traits]. Those traits that seem to link Latimeria and tetrapods are arguably due to convergent evolution or reversals and not to common descent. In this way, the molecular tree facilitates an evolutionary interpretation of the morphological differences among the living forms. We recommended that the extinct groups of lobe-finned fishes be placed onto the molecular tree that has lungfishes and not the coelacanth more closely related to tetrapods. The placement of fossils would help to further interpret the sequence of morphological events and innovations associated with the origin of tetrapods but appears to be problematic because the quality of fossils is not always high enough, and differences among paleontologists in the interpretation of the fossils have stood in the way of a consensus opinion for the branching order among lobefinned fishes. Marshall and Schultze (1992) criticized the morphological analysis presented by Meyer and Wilson (1990) and suggest that 13 of the 14 morphological traits that support the sister group relationship of lungfishes and tetrapods are not shared derived characters. Here we present further alternative viewpoints to the ones of Marshall and Schultze (1992) from the paleontological literature. We argue that all available information (paleontological, neontological, and molecular data) and rigorous cladistic methodology should be used when relating fossils and extant taxa in a phylogenetic framework.

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Year:  1992        PMID: 1501250     DOI: 10.1007/bf00183221

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


  15 in total

1.  Monophyletic origin of Lake Victoria cichlid fishes suggested by mitochondrial DNA sequences.

Authors:  A Meyer; T D Kocher; P Basasibwaki; A C Wilson
Journal:  Nature       Date:  1990-10-11       Impact factor: 49.962

2.  Close tetrapod relationships of the coelacanth Latimeria indicated by haemoglobin sequences.

Authors:  T Gorr; T Kleinschmidt; H Fricke
Journal:  Nature       Date:  1991-05-30       Impact factor: 49.962

3.  Phylogenetic relationships of neopterygian fishes, inferred from mitochondrial DNA sequences.

Authors:  B B Normark; A R McCune; R G Harrison
Journal:  Mol Biol Evol       Date:  1991-11       Impact factor: 16.240

4.  CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP.

Authors:  Joseph Felsenstein
Journal:  Evolution       Date:  1985-07       Impact factor: 3.694

5.  PATTERNS OF VARIATION IN LEVELS OF HOMOPLASY.

Authors:  Michael J Sanderson; Michael J Donoghue
Journal:  Evolution       Date:  1989-12       Impact factor: 3.694

6.  Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers.

Authors:  T D Kocher; W K Thomas; A Meyer; S V Edwards; S Pääbo; F X Villablanca; A C Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

7.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

8.  Origin of tetrapods inferred from their mitochondrial DNA affiliation to lungfish.

Authors:  A Meyer; A C Wilson
Journal:  J Mol Evol       Date:  1990-11       Impact factor: 2.395

Review 9.  Relative importance of molecular, neontological, and paleontological data in understanding the biology of the vertebrate invasion of land.

Authors:  C Marshall; H P Schultze
Journal:  J Mol Evol       Date:  1992-08       Impact factor: 2.395

10.  Inner ear of the coelacanth fish Latimeria has tetrapod affinities.

Authors:  B Fritzsch
Journal:  Nature       Date:  1987 May 14-20       Impact factor: 49.962

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  19 in total

1.  The complete nucleotide sequence of the mitochondrial genome of the lungfish (Protopterus dolloi) supports its phylogenetic position as a close relative of land vertebrates.

Authors:  R Zardoya; A Meyer
Journal:  Genetics       Date:  1996-04       Impact factor: 4.562

2.  Complete mitochondrial genome sequences of the South american and the Australian lungfish: testing of the phylogenetic performance of mitochondrial data sets for phylogenetic problems in tetrapod relationships.

Authors:  Henner Brinkmann; Angelika Denk; Jürgen Zitzler; Jean J Joss; Axel Meyer
Journal:  J Mol Evol       Date:  2004-12       Impact factor: 2.395

3.  The complete DNA sequence of the mitochondrial genome of a "living fossil," the coelacanth (Latimeria chalumnae).

Authors:  R Zardoya; A Meyer
Journal:  Genetics       Date:  1997-07       Impact factor: 4.562

4.  Analysis of the transcriptome of the Indonesian coelacanth Latimeria menadoensis.

Authors:  Alberto Pallavicini; Adriana Canapa; Marco Barucca; Jessica Alfőldi; Maria Assunta Biscotti; Francesco Buonocore; Gianluca De Moro; Federica Di Palma; Anna Maria Fausto; Mariko Forconi; Marco Gerdol; Daisy Monica Makapedua; Jason Turner-Meier; Ettore Olmo; Giuseppe Scapigliati
Journal:  BMC Genomics       Date:  2013-08-08       Impact factor: 3.969

5.  Evolutionary relationships of the coelacanth, lungfishes, and tetrapods based on the 28S ribosomal RNA gene.

Authors:  R Zardoya; A Meyer
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-28       Impact factor: 11.205

6.  Lungfishes, like tetrapods, possess a vomeronasal system.

Authors:  Agustín González; Ruth Morona; Jesús M López; Nerea Moreno; R Glenn Northcutt
Journal:  Front Neuroanat       Date:  2010-09-01       Impact factor: 3.856

7.  Relationship among coelacanths, lungfishes, and tetrapods: a phylogenetic analysis based on mitochondrial cytochrome oxidase I gene sequences.

Authors:  S Yokobori; M Hasegawa; T Ueda; N Okada; K Nishikawa; K Watanabe
Journal:  J Mol Evol       Date:  1994-06       Impact factor: 2.395

Review 8.  Relative importance of molecular, neontological, and paleontological data in understanding the biology of the vertebrate invasion of land.

Authors:  C Marshall; H P Schultze
Journal:  J Mol Evol       Date:  1992-08       Impact factor: 2.395

9.  Phylogeny of African monkeys based upon mitochondrial 12S rRNA sequences.

Authors:  A C van der Kuyl; C L Kuiken; J T Dekker; J Goudsmit
Journal:  J Mol Evol       Date:  1995-02       Impact factor: 2.395

10.  Nuclear protein-coding genes support lungfish and not the coelacanth as the closest living relatives of land vertebrates.

Authors:  Henner Brinkmann; Byrappa Venkatesh; Sydney Brenner; Axel Meyer
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-22       Impact factor: 11.205

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