甜菜杂种H20抗病启动基因NPR1附近的LTR反转录转座子巢

International journal of plant genomics Pub Date : 2009-01-01 Epub Date: 2009-04-15 DOI:10.1155/2009/576742
David Kuykendall, Jonathan Shao, Kenneth Trimmer
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引用次数: 19

摘要

通过LTR_STRUC分析,在甜菜杂交品种US H20中编码NPR1抗病激活因子和HSF-样蛋白的核心基因附近发现了一个长末端重复(LTR)反转录转座子(RTRs)巢。SCHULTE是一个10833 bp的LTR逆转录转座子,其1372 bp的LTRs有0.7%的差异,具有两个意想不到的内含子的orf,但编码具有与Ty1/复制型逆转录转座子相似的rve和Rvt2结构域的逆转录酶和一种假设的蛋白质。SCHULTE与TIGR植物重复序列数据库(PRD)中所有四个植物家族的重复DNA元素进行了显著的核苷酸BLAST比对;番茄中ToRTL1的核苷酸序列比对效果最好。另一个甜菜LTR反转录转座子SCHMIDT长度为11 565 bp,其长度为2561 bp的LTR彼此具有100%的同源性,并且与drv具有超过10%长度的98-99%的核苷酸序列同源性,drv是一个高度重复的相对较小的DNA序列家族,广泛分布在甜菜基因组中。施密特在一个ORF中编码了一个完整的吉普赛样多蛋白。利用LTR_STRUC对上述两个LTR反转录转座子的缺失进行分析发现,SCHULTE和SCHMIDT插入了一个较老的LTR反转录转座子,在甜菜杂交株US H20中,在NPR1上游约10 Kb处形成了一个巢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Nest of LTR Retrotransposons Adjacent the Disease Resistance-Priming Gene NPR1 in Beta vulgaris L. U.S. Hybrid H20.

A nest of long terminal repeat (LTR) retrotransposons (RTRs), discovered by LTR_STRUC analysis, is near core genes encoding the NPR1 disease resistance-activating factor and a heat-shock-factor-(HSF-) like protein in sugarbeet hybrid US H20. SCHULTE, a 10 833 bp LTR retrotransposon, with 1372 bp LTRs that are 0.7% divergent, has two ORFs with unexpected introns but encoding a reverse transcriptase with rve and Rvt2 domains similar to Ty1/copia-type retrotransposons and a hypothetical protein. SCHULTE produced significant nucleotide BLAST alignments with repeat DNA elements from all four families of plants represented in the TIGR plant repeat database (PRD); the best nucleotide sequence alignment was to ToRTL1 in Lycopersicon esculentum. A second sugarbeet LTR retrotransposon, SCHMIDT, 11 565 bp in length, has 2561 bp LTRs that share 100% identity with each other and share 98-99% nucleotide sequence identity over 10% of their length with DRVs, a family of highly repetitive, relatively small DNA sequences that are widely dispersed over the sugarbeet genome. SCHMIDT encodes a complete gypsy-like polyprotein in a single ORF. Analysis using LTR_STRUC of an in silico deletion of both of the above two LTR retrotransposons found that SCHULTE and SCHMIDT had inserted within an older LTR retrotransposon, resulting in a nest that is only about 10 Kb upstream of NPR1 in sugarbeet hybrid US H20.

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