日本莲基因组的结构分析。2覆盖基因组6.5 mb区域的65个TAC克隆的序列特征和图谱。

Yasukazu Nakamura, T. Kaneko, E. Asamizu, Tomohiko Kato, Shusei Sato, S. Tabata
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引用次数: 37

摘要

利用表达序列标签(est)、cDNA和基因信息,从日本莲苗mg20基因组文库中筛选出65个具有转化能力的人工染色体(TAC)克隆,并对其核苷酸序列进行了测定。TAC克隆的平均插入长度约为100 kb,本研究测序区域的总长度为6,556,100 bp。加上先前报道的56个TAC克隆的核苷酸序列,目前测序的区域总数为12029295 bp。通过与蛋白质数据库和EST数据库中的序列比对,并通过计算机程序进行基因建模分析,在新测序区域中共鉴定出711个已知或预测功能的潜在蛋白质编码基因,239个基因片段和90个假基因。平均基因密度为1个基因/9140 bp。分配基因的平均长度为2.6 kb,明显大于拟南芥基因组(6451个基因的平均长度为1.9 kb)。在约73%的潜在基因中鉴定出内含子,每个基因平均内含子数和长度分别为3.4 bp和377 bp。根据获得的基因组克隆核苷酸序列,生成简单序列重复长度多态性(SSLP)或衍生的cleaved amplified polymorphic sequence (dCAPS)标记,并利用日本l.l japonicus Gifu B-129和Miyakojima MG-20杂交获得的F2定位群体,将每个克隆定位到连锁图谱上。序列数据、基因信息和图谱信息可通过万维网(http://www.kazusa.or.jp/lotus/)获得。
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Structural analysis of a Lotus japonicus genome. II. Sequence features and mapping of sixty-five TAC clones which cover the 6.5-mb regions of the genome.
Sixty-five TAC (transformation-competent artificial chromosomes) clones were selected from a genomic library of Lotus japonicus accession MG-20 based on the sequence information of expressed sequences tags (ESTs), cDNA and gene information, and their nucleotide sequences were determined. The average insert size of the TAC clone was approximately 100 kb, and the total length of the sequenced regions in this study is 6,556,100 bp. Together with the nucleotide sequences of 56 TAC clones previously reported, the regions sequenced so far total 12,029,295 bp. By comparison with the sequences in protein and EST databases and by analysis with computer programs for gene modeling, a total of 711 potential protein-encoding genes with known or predicted functions, 239 gene segments and 90 pseudogenes were identified in the newly sequenced regions. The average gene density assigned so far was 1 gene/9140 bp. The average length of the assigned genes was 2.6 kb, which is considerably larger than that assigned in the Arabidopsis thaliana genome (1.9 kb for 6451 genes). Introns were identified in approximately 73% of the potential genes, and the average number and length of the introns per gene were 3.4 and 377 bp, respectively. Simple sequence repeat length polymorphism (SSLP) or derived cleaved amplified polymorphic sequence (dCAPS) markers were generated based on the nucleotide sequences of the genomic clones obtained, and each clone was mapped onto the linkage map using the F2 mapping population derived from a cross of two accessions of L. japonicus, Gifu B-129 and Miyakojima MG-20. The sequence data, gene information and mapping information are available through the World Wide Web at http://www.kazusa.or.jp/lotus/.
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