Molecules, fossils, and the origin of tetrapods
- PMID: 1501250
- DOI: 10.1007/BF00183221
Molecules, fossils, and the origin of tetrapods
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.
Similar articles
-
Evolutionary relationships of the coelacanth, lungfishes, and tetrapods based on the 28S ribosomal RNA gene.Proc Natl Acad Sci U S A. 1996 May 28;93(11):5449-54. doi: 10.1073/pnas.93.11.5449. Proc Natl Acad Sci U S A. 1996. PMID: 8643595 Free PMC article.
-
Origin of tetrapods inferred from their mitochondrial DNA affiliation to lungfish.J Mol Evol. 1990 Nov;31(5):359-64. doi: 10.1007/BF02106050. J Mol Evol. 1990. PMID: 2124628
-
Relative importance of molecular, neontological, and paleontological data in understanding the biology of the vertebrate invasion of land.J Mol Evol. 1992 Aug;35(2):93-101. doi: 10.1007/BF00183220. J Mol Evol. 1992. PMID: 1501257 Review.
-
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.J Mol Evol. 2004 Dec;59(6):834-48. doi: 10.1007/s00239-004-0122-8. J Mol Evol. 2004. PMID: 15599515
-
Molecular phylogenetic information on the identity of the closest living relative(s) of land vertebrates.Naturwissenschaften. 1997 Sep;84(9):389-97. doi: 10.1007/s001140050415. Naturwissenschaften. 1997. PMID: 9353759 Review.
Cited by
-
Lungfishes, like tetrapods, possess a vomeronasal system.Front Neuroanat. 2010 Sep 1;4:130. doi: 10.3389/fnana.2010.00130. eCollection 2010. Front Neuroanat. 2010. PMID: 20941371 Free PMC article.
-
New nucleotide sequence data on the EMBL File Server.Nucleic Acids Res. 1992 Nov 11;20(21):5865-85. doi: 10.1093/nar/20.21.5865. Nucleic Acids Res. 1992. PMID: 1454557 Free PMC article. No abstract available.
-
Asymmetric paralog evolution between the "cryptic" gene Bmp16 and its well-studied sister genes Bmp2 and Bmp4.Sci Rep. 2019 Feb 28;9(1):3136. doi: 10.1038/s41598-019-40055-1. Sci Rep. 2019. PMID: 30816280 Free PMC article.
-
Evolutionary relationships of the coelacanth, lungfishes, and tetrapods based on the 28S ribosomal RNA gene.Proc Natl Acad Sci U S A. 1996 May 28;93(11):5449-54. doi: 10.1073/pnas.93.11.5449. Proc Natl Acad Sci U S A. 1996. PMID: 8643595 Free PMC article.
-
Rise of the earliest tetrapods: an early Devonian origin from marine environment.PLoS One. 2011;6(7):e22136. doi: 10.1371/journal.pone.0022136. Epub 2011 Jul 14. PLoS One. 2011. PMID: 21779385 Free PMC article.
References
Publication types
MeSH terms
Substances
Associated data
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions