ArticlePloS one2009
Intron evolution: testing hypotheses of intron evolution using the phylogenomics of tetraspanins.
Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
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21 citing papers in PubMed, 43 citations in OpenAlex.
- MixtureFinder: Estimating DNA Mixture Models for Phylogenetic Analyses.Molecular biology and evolution · 2025Article
- Origin and Evolution of RAS Membrane Targeting.Oncogene · 2023Article
- Origin and evolution of RAS oncoprotein membrane targeting.Research square · 2023Article
- Open conformation of tetraspanins shapes interaction partner networks on cell membranes.The EMBO journal · 2020Article
- Differential tetraspanin genes expression and subcellular localization during mutualistic interactions in Phaseolus vulgaris.PloS one · 2019Article
- Genome-wide analyses supported by RNA-Seq reveal non-canonical splice sites in plant genomes.BMC genomics · 2018Article
- Phosphotyrosine phosphatase R3 receptors: Origin, evolution and structural diversification.PloS one · 2017Article
- The Tetraspanin-Associated Uroplakins Family (UPK2/3) Is Evolutionarily Related to PTPRQ, a Phosphotyrosine Phosphatase Receptor.PloS one · 2017Article
- Comprehensive Expression Profiling of Rice Tetraspanin Genes Reveals Diverse Roles During Development and Abiotic Stress.Frontiers in plant science · 2015Article
- Generation of divergent uroplakin tetraspanins and their partners during vertebrate evolution: identification of novel uroplakins.BMC evolutionary biology · 2014Article
- Molecular cloning, sequence characterization and expression analysis of a CD63 homologue from the coleopteran beetle, Tenebrio molitor.International journal of molecular sciences · 2013Article
- Analysis of the Ush2a gene in medaka fish (Oryzias latipes).PloS one · 2013Article
- PIECE: a database for plant gene structure comparison and evolution.Nucleic acids research · 2013Article
- Origin and evolution of spliceosomal introns.Biology direct · 2012Review
- A transcriptomic analysis of Echinococcus granulosus larval stages: implications for parasite biology and host adaptation.PLoS neglected tropical diseases · 2012Article
- DOR/Tp53inp2 and Tp53inp1 constitute a metazoan gene family encoding dual regulators of autophagy and transcription.PloS one · 2012Article
- Identification and characterization of six novel tetraspanins from Schistosoma japonicum.Parasites & vectors · 2011Article
- Phylogenetic distribution of intron positions in alpha-amylase genes of bilateria suggests numerous gains and losses.PloS one · 2011Article
- The evolution of vertebrate tetraspanins: gene loss, retention, and massive positive selection after whole genome duplications.BMC evolutionary biology · 2010Article
- Evolutionary genetic insights into Plasmodium falciparum functional genes.Parasitology research · 2010Article
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Authors and funding
4 authors at 3 institutions in 2 countries.
Funding
Abstract
backgroundAlthough large scale informatics studies on introns can be useful in making broad inferences concerning patterns of intron gain and loss, more specific questions about intron evolution at a finer scale can be addressed using a gene family where structure and function are well known. Genome wide surveys of tetraspanins from a broad array of organisms with fully sequenced genomes are an excellent means to understand specifics of intron evolution. Our approach incorporated several new fully sequenced genomes that cover the major lineages of the animal kingdom as well as plants, protists and fungi. The analysis of exon/intron gene structure in such an evolutionary broad set of genomes allowed us to identify ancestral intron structure in tetraspanins throughout the eukaryotic tree of life. METHODOLOGY/PRINCIPAL
findingsWe performed a phylogenomic analysis of the intron/exon structure of the tetraspanin protein family. In addition, to the already characterized tetraspanin introns numbered 1 through 6 found in animals, three additional ancient, phase 0 introns we call 4a, 4b and 4c were found. These three novel introns in combination with the ancestral introns 1 to 6, define three basic tetraspanin gene structures which have been conserved throughout the animal kingdom. Our phylogenomic approach also allows the estimation of the time at which the introns of the 33 human tetraspanin paralogs appeared, which in many cases coincides with the concomitant acquisition of new introns. On the other hand, we observed that new introns (introns other than 1-6, 4a, b and c) were not randomly inserted into the tetraspanin gene structure. The region of tetraspanin genes corresponding to the small extracellular loop (SEL) accounts for only 10.5% of the total sequence length but had 46% of the new animal intron insertions. CONCLUSIONS/SIGNIFICANCE: Our results indicate that tests of intron evolution are strengthened by the phylogenomic approach with specific gene families like tetraspanins. These tests add to our understanding of genomic innovation coupled to major evolutionary divergence events, functional constraints and the timing of the appearance of evolutionary novelty.
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