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水稻及其近缘物种中一个具有转录活性的玉米类MuDR转座元件

A transcriptionally active maize MuDR-like transposable element in rice and its relatives.

作者信息

Asakura N, Nakamura C, Ishii T, Kasai Y, Yoshida S

机构信息

Laboratory of Biology, Faculty of Engineering, Kanagawa University, Yokohama 221-8686, Japan.

出版信息

Mol Genet Genomics. 2002 Nov;268(3):321-30. doi: 10.1007/s00438-002-0737-7. Epub 2002 Aug 15.

DOI:10.1007/s00438-002-0737-7
PMID:12436254
Abstract

Two Mu-like transposable elements were cloned from a rice genomic library using a partial cDNA clone that exhibits high homology to the mudrA gene of the maize element MuDR. Database searches led to the identification of six other sequences that carried highly homologous terminal inverted repeats (TIRs). All the rice elements possessed approximately 200-bp TIRs, and four were flanked by 9-bp target-site duplications (TSDs). The longer of the two cloned elements, OsMu4-2, could potentially encode a protein colinear with a MURA-like transposase, but it had stop codons in the coding region indicating that it is a pseudogene. All the other elements had large internal deletions. Direct dinucleotide repeats were found in two elements at positions flanking the deleted regions, suggesting that the deletions arose via the interrupted-gap-repair mechanism. Sequences related to empty sites of insertion were found in OsMu4-2 and one of the elements identified in the databases. These results provide evidence that the rice OsMu element was active and transposed in the past. Analysis of OsMu4-2 cDNAs revealed two types of transcripts produced by alternative splicing. Genomic Southern analysis suggested that OsMu4-2 was conserved in rice species with the A genome, but a deleted version was unique to japonica subspecies. Some wild rice species harbored paralogous copies of the OsMu element.

摘要

利用一个与玉米转座元件MuDR的mudrA基因具有高度同源性的部分cDNA克隆,从水稻基因组文库中克隆出两个类Mu转座元件。数据库搜索鉴定出另外六个携带高度同源末端反向重复序列(TIR)的序列。所有水稻元件都具有约200bp的TIR,其中四个元件两侧有9bp的靶位点重复序列(TSD)。两个克隆元件中较长的OsMu4-2可能编码一种与类MURA转座酶共线性的蛋白质,但它在编码区有终止密码子,表明它是一个假基因。所有其他元件都有大片段内部缺失。在两个元件缺失区域两侧的位置发现了直接二核苷酸重复序列,表明这些缺失是通过中断间隙修复机制产生的。在OsMu4-2和数据库中鉴定出的一个元件中发现了与插入空位相关的序列。这些结果提供了水稻OsMu元件过去具有活性并发生转座的证据。对OsMu4-2 cDNA的分析揭示了由可变剪接产生的两种转录本类型。基因组Southern分析表明,OsMu4-2在具有A基因组的水稻物种中是保守的,但一个缺失版本是粳稻亚种特有的。一些野生稻物种含有OsMu元件的旁系同源拷贝。

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