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利用EST数据对海鞘线粒体DNA进行转录本定位和基因组注释。

Transcript mapping and genome annotation of ascidian mtDNA using EST data.

作者信息

Gissi Carmela, Pesole Graziano

机构信息

Dipartimento di Scienze Biomolecolari e Biotecnologie, Università di Milano, Milano, Italy.

出版信息

Genome Res. 2003 Sep;13(9):2203-12. doi: 10.1101/gr.1227803. Epub 2003 Aug 12.

Abstract

Mitochondrial transcripts of two ascidian species were reconstructed through sequence assembly of publicly available ESTs resembling mitochondrial DNA sequences (mt-ESTs). This strategy allowed us to analyze processing and mapping of the mitochondrial transcripts and to investigate the gene organization of a previously uncharacterized mitochondrial genome (mtDNA). This new strategy would greatly facilitate the sequencing and annotation of mtDNAs. In Ciona intestinalis, the assembled mt-ESTs covered 22 mitochondrial genes ( approximately 12,000 bp) and provided the partial sequence of the mtDNA and the prediction of its gene organization. Such sequences were confirmed by amplification and sequencing of the entire Ciona mtDNA. For Halocynthia roretzi, for which the mtDNA sequence was already available, the inferred mt transcripts allowed better definition of gene boundaries (16S rRNA, ND1, ATP6, and tRNA-Ser genes) and the identification of a new gene (an additional Phe-tRNA). In both species, polycistronic and immature transcripts, creation of stop codons by polyadenylation, tRNA signal processing, and rRNA transcript termination signals were identified, thus suggesting that the main features of mitochondrial transcripts are conserved in Chordata.

摘要

通过对类似于线粒体DNA序列(mt-ESTs)的公开可用ESTs进行序列组装,重建了两种海鞘的线粒体转录本。这种策略使我们能够分析线粒体转录本的加工和定位,并研究以前未表征的线粒体基因组(mtDNA)的基因组织。这种新策略将极大地促进mtDNA的测序和注释。在玻璃海鞘中,组装的mt-ESTs覆盖了22个线粒体基因(约12,000 bp),提供了mtDNA的部分序列及其基因组织的预测。通过对整个玻璃海鞘mtDNA的扩增和测序,证实了这些序列。对于已具有mtDNA序列的柄海鞘,推断的mt转录本能够更好地定义基因边界(16S rRNA、ND1、ATP6和tRNA-Ser基因),并鉴定出一个新基因(一个额外的苯丙氨酸tRNA)。在这两个物种中,均鉴定出多顺反子和未成熟转录本、通过多聚腺苷酸化产生终止密码子、tRNA信号加工以及rRNA转录本终止信号,因此表明线粒体转录本的主要特征在脊索动物中是保守的。

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