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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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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