Evidence map›Paper›PMID 20147436›Full record

ArticleMolecular biology and evolution2010

Internal and external paralogy in the evolution of tropomyosin genes in metazoans.

Manuel Irimia, Ignacio Maeso, Peter W Gunning, Jordi Garcia-Fernàndez, Scott William Roy

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.8field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Widespread recurrent evolution of genomic features.Genome biology and evolution · 2012
    Review
  7. Article
  8. Article
  9. Article
  10. Molecular architecture of muscles in an acoel and its evolutionary implications.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2011
    Article
  11. Evolutionarily conserved surface residues constitute actin binding sites of tropomyosin.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  12. Stepwise assembly of the Nova-regulated alternative splicing network in the vertebrate brain.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  13. Article
  14. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 3 countries.

Manuel IrimiaDepartament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Ignacio Maeso
Peter W Gunning
Jordi Garcia-Fernàndez
Scott William Roy
Universitat de Barcelona · ESNational Center for Biotechnology Information · USUNSW Sydney · AU

Funding

Intramural NIH HHS
6 · The paper itself

Abstract

Nature contains a tremendous diversity of forms both at the organismal and genomic levels. This diversity motivates the twin central questions of molecular evolution: what are the molecular mechanisms of adaptation, and what are the functional consequences of genomic diversity. We report a 22-species comparative analysis of tropomyosin (PPM) genes, which exist in a variety of forms and are implicated in the emergence of a wealth of cellular functions, including the novel muscle functions integral to the functional diversification of bilateral animals. TPM genes encode either or both of long-form [284 amino acid (aa)] and short-form (approximately 248 aa) proteins. Consistent with a role of TPM diversification in the origins and radiation of bilaterians, we find evidence that the muscle-specific long-form protein arose in proximal bilaterian ancestors (the bilaterian 'stem'). Duplication of the 5' end of the gene led to alternative promoters encoding long- and short-form transcripts with distinct functions. This dual-function gene then underwent strikingly parallel evolution in different bilaterian lineages. In each case, recurrent tandem exon duplication and mutually exclusive alternative splicing of the duplicates, with further association between these alternatively spliced exons along the gene, led to long- and short-form-specific exons, allowing for gradual emergence of alternative "internal paralogs" within the same gene. We term these Mutually exclusively Alternatively spliced Tandemly duplicated Exon sets "MATEs". This emergence of internal paralogs in various bilaterians has employed every single TPM exon in at least one lineage and reaches striking levels of divergence with up to 77% of long- and short-form transcripts being transcribed from different genomic regions. Interestingly, in some lineages, these internal alternatively spliced paralogs have subsequently been "externalized" by full gene duplication and reciprocal retention/loss of the two transcript isoforms, a particularly clear case of evolution by subfunctionalization. This parallel evolution of TPM genes in diverse metazoans attests to common selective forces driving divergence of different gene transcripts and represents a striking case of emergence of evolutionary novelty by alternative splicing.

Indexed as

Alternative SplicingEvolution, MolecularGene DuplicationAmino Acid SequenceAnimalsBase SequenceExonsMolecular Sequence DataPhylogenySequence Homology, Amino AcidSequence Homology, Nucleic AcidTropomyosinTropomyosin

Identifiers

PMID20147436
PMCPMC2912468
OpenAlexW2098872898

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.