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Early vertebrate chromosome duplications and the evolution of the neuropeptide Y receptor gene regions

Authors: Larsson, T.A; Olsson, F; Sundstrom, G; Lundin, L.-G; Brenner, S; Venkatesh, B; Larhammar, D;

Early vertebrate chromosome duplications and the evolution of the neuropeptide Y receptor gene regions

Abstract

AbstractBackgroundOne of the many gene families that expanded in early vertebrate evolution is the neuropeptide (NPY) receptor family of G-protein coupled receptors. Earlier work by our lab suggested that several of the NPY receptor genes found in extant vertebrates resulted from two genome duplications before the origin of jawed vertebrates (gnathostomes) and one additional genome duplication in the actinopterygian lineage, based on their location on chromosomes sharing several gene families. In this study we have investigated, in five vertebrate genomes, 45 gene families with members close to the NPY receptor genes in the compact genomes of the teleost fishesTetraodon nigroviridisandTakifugu rubripes. These correspond toHomo sapienschromosomes 4, 5, 8 and 10.ResultsChromosome regions with conserved synteny were identified and confirmed by phylogenetic analyses inH. sapiens, M. musculus, D. rerio, T. rubripesandT. nigroviridis. 26 gene families, including the NPY receptor genes, (plus 3 described recently by other labs) showed a tree topology consistent with duplications in early vertebrate evolution and in the actinopterygian lineage, thereby supporting expansion through block duplications. Eight gene families had complications that precluded analysis (such as short sequence length or variable number of repeated domains) and another eight families did not support block duplications (because the paralogs in these families seem to have originated in another time window than the proposed genome duplication events). RT-PCR carried out with several tissues inT. rubripesrevealed that all five NPY receptors were expressed in the brain and subtypes Y2, Y4 and Y8 were also expressed in peripheral organs.ConclusionWe conclude that the phylogenetic analyses and chromosomal locations of these gene families support duplications of large blocks of genes or even entire chromosomes. Thus, these results are consistent with two early vertebrate tetraploidizations forming a paralogon comprising human chromosomes 4, 5, 8 and 10 and one teleost tetraploidization. The combination of positional and phylogenetic data further strengthens the identification of orthologs and paralogs in the NPY receptor family.

Country
Singapore
Keywords

mitogen activated protein kinase phosphatase 1, phylogeny, Mice, vertebrate, Gene Duplication, ADAM protein, animal, genetics, chromosome, Phylogeny, mitogen activated protein kinase, Reverse Transcriptase Polymerase Chain Reaction, ADAMTS3 protein, synteny, article, chromosome duplication, Gnathostomata (vertebrate), actin binding protein, Multigene Family, fibroblast growth factor receptor, LIM protein, Vertebrates, Research Article, zinc finger protein, 570, oxoglutarate dehydrogenase, tachykinin receptor, Evolution, G protein coupled receptor, Chromosomes, reverse transcription polymerase chain reaction, Evolution, Molecular, annexin, chromosome 10, ankyrin, statistical analysis, evolution, chromosome 8, QH359-425, chromosome 5, Mus musculus, Animals, Humans, neuropeptide Y receptor, human, chromosome 4, ADAMTS14 protein, paralogy, multigene family, mouse, Ecology, Evolution, Behavior and Systematics, Takifugu rubripes, secreted frizzled related protein 1, nonhuman, Danio rerio, Homo sapiens, molecular evolution, Tetraodontiformes, gene duplication, nucleotide sequence, ADAMTS2 protein, RNA binding protein, Receptors, Neuropeptide Y, Takifugu, tetraspanin, puffer fish

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
61
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