Huntingtin gene evolution in Chordata and its peculiar features in the ascidian <it>Ciona </it>genus

<p>Abstract</p> <p>Background</p> <p>To gain insight into the evolutionary features of the huntingtin (htt) gene in Chordata, we have sequenced and characterized the full-length htt mRNA in the ascidian <it>Ciona intestinalis</it>, a basal chordate emerging...

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Main Authors: Cattaneo Elena, Pesole Graziano, Gissi Carmela, Tartari Marzia
Format: Article
Language:English
Published: BMC 2006-11-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/7/288
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spelling doaj-9bdccd8eb8204e49a1f439e499a9ffc02020-11-25T01:04:48ZengBMCBMC Genomics1471-21642006-11-017128810.1186/1471-2164-7-288Huntingtin gene evolution in Chordata and its peculiar features in the ascidian <it>Ciona </it>genusCattaneo ElenaPesole GrazianoGissi CarmelaTartari Marzia<p>Abstract</p> <p>Background</p> <p>To gain insight into the evolutionary features of the huntingtin (htt) gene in Chordata, we have sequenced and characterized the full-length htt mRNA in the ascidian <it>Ciona intestinalis</it>, a basal chordate emerging as new invertebrate model organism. Moreover, taking advantage of the availability of genomic and EST sequences, the htt gene structure of a number of chordate species, including the cogeneric ascidian <it>Ciona savignyi</it>, and the vertebrates <it>Xenopus </it>and <it>Gallus </it>was reconstructed.</p> <p>Results</p> <p>The <it>C. intestinalis </it>htt transcript exhibits some peculiar features, such as spliced leader trans-splicing in the 98 nt-long 5' untranslated region (UTR), an alternative splicing in the coding region, eight alternative polyadenylation sites, and no similarities of both 5' and 3'UTRs compared to homologs of the cogeneric <it>C. savignyi</it>. The predicted protein is 2946 amino acids long, shorter than its vertebrate homologs, and lacks the polyQ and the polyP stretches found in the the N-terminal regions of mammalian homologs. The exon-intron organization of the htt gene is almost identical among vertebrates, and significantly conserved between <it>Ciona </it>and vertebrates, allowing us to hypothesize an ancestral chordate gene consisting of at least 40 coding exons.</p> <p>Conclusion</p> <p>During chordate diversification, events of gain/loss, sliding, phase changes, and expansion of introns occurred in both vertebrate and ascidian lineages predominantly in the 5'-half of the htt gene, where there is also evidence of lineage-specific evolutionary dynamics in vertebrates. On the contrary, the 3'-half of the gene is highly conserved in all chordates at the level of both gene structure and protein sequence. Between the two <it>Ciona </it>species, a fast evolutionary rate and/or an early divergence time is suggested by the absence of significant similarity between UTRs, protein divergence comparable to that observed between mammals and fishes, and different distribution of repetitive elements.</p> http://www.biomedcentral.com/1471-2164/7/288
collection DOAJ
language English
format Article
sources DOAJ
author Cattaneo Elena
Pesole Graziano
Gissi Carmela
Tartari Marzia
spellingShingle Cattaneo Elena
Pesole Graziano
Gissi Carmela
Tartari Marzia
Huntingtin gene evolution in Chordata and its peculiar features in the ascidian <it>Ciona </it>genus
BMC Genomics
author_facet Cattaneo Elena
Pesole Graziano
Gissi Carmela
Tartari Marzia
author_sort Cattaneo Elena
title Huntingtin gene evolution in Chordata and its peculiar features in the ascidian <it>Ciona </it>genus
title_short Huntingtin gene evolution in Chordata and its peculiar features in the ascidian <it>Ciona </it>genus
title_full Huntingtin gene evolution in Chordata and its peculiar features in the ascidian <it>Ciona </it>genus
title_fullStr Huntingtin gene evolution in Chordata and its peculiar features in the ascidian <it>Ciona </it>genus
title_full_unstemmed Huntingtin gene evolution in Chordata and its peculiar features in the ascidian <it>Ciona </it>genus
title_sort huntingtin gene evolution in chordata and its peculiar features in the ascidian <it>ciona </it>genus
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2006-11-01
description <p>Abstract</p> <p>Background</p> <p>To gain insight into the evolutionary features of the huntingtin (htt) gene in Chordata, we have sequenced and characterized the full-length htt mRNA in the ascidian <it>Ciona intestinalis</it>, a basal chordate emerging as new invertebrate model organism. Moreover, taking advantage of the availability of genomic and EST sequences, the htt gene structure of a number of chordate species, including the cogeneric ascidian <it>Ciona savignyi</it>, and the vertebrates <it>Xenopus </it>and <it>Gallus </it>was reconstructed.</p> <p>Results</p> <p>The <it>C. intestinalis </it>htt transcript exhibits some peculiar features, such as spliced leader trans-splicing in the 98 nt-long 5' untranslated region (UTR), an alternative splicing in the coding region, eight alternative polyadenylation sites, and no similarities of both 5' and 3'UTRs compared to homologs of the cogeneric <it>C. savignyi</it>. The predicted protein is 2946 amino acids long, shorter than its vertebrate homologs, and lacks the polyQ and the polyP stretches found in the the N-terminal regions of mammalian homologs. The exon-intron organization of the htt gene is almost identical among vertebrates, and significantly conserved between <it>Ciona </it>and vertebrates, allowing us to hypothesize an ancestral chordate gene consisting of at least 40 coding exons.</p> <p>Conclusion</p> <p>During chordate diversification, events of gain/loss, sliding, phase changes, and expansion of introns occurred in both vertebrate and ascidian lineages predominantly in the 5'-half of the htt gene, where there is also evidence of lineage-specific evolutionary dynamics in vertebrates. On the contrary, the 3'-half of the gene is highly conserved in all chordates at the level of both gene structure and protein sequence. Between the two <it>Ciona </it>species, a fast evolutionary rate and/or an early divergence time is suggested by the absence of significant similarity between UTRs, protein divergence comparable to that observed between mammals and fishes, and different distribution of repetitive elements.</p>
url http://www.biomedcentral.com/1471-2164/7/288
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