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有效隔离小麦基因组中的逆转座子和重复 DNA 家族。

Effective isolation of retrotransposons and repetitive DNA families from the wheat genome.

机构信息

Molecular Genetics Laboratory, Faculty of Agriculture, Tottori University, Tottori 680-8553, Japan.

出版信息

J Integr Plant Biol. 2010 Jul;52(7):679-91. doi: 10.1111/j.1744-7909.2010.00954.x.

Abstract

New classes of repetitive DNA elements were effectively identified by isolating small fragments of the elements from the wheat genome. A wheat A genome library was constructed from Triticum monococcum by degenerate cleavage with EcoO109I, the recognition sites of which consisted of 5'-PuGGNCCPy-3' multi-sequences. Three novel repetitive sequences pTm6, pTm69 and pTm58 derived from the A genome were screened and tested for high copy number using a blotting approach. pTm6 showed identity with integrase domains of the barley Ty1-Copia-retrotransposon BARE-1 and pTm58 showed similarity to the barley Ty3-gypsy-like retrotransposon Romani. pTm69, however, constituted a tandem array with useful genomic specificities, but did not share any identity with known repetitive elements. This study also sought to isolate wheat D-genome-specific repetitive elements regardless of the level of methylation, by genomic subtraction. Total genomic DNA of Aegilops tauschii was cleaved into short fragments with a methylation-insensitive 4 bp cutter, MboI, and then common DNA sequences between Ae. tauschii and Triticum turgidum were subtracted by annealing with excess T. turgidum genomic DNA. The D genome repetitive sequence pAt1 was isolated and used to identify an additional novel repetitive sequence family from wheat bacterial artificial chromosomes with a size range of 1 395-1 850 bp. The methods successfully led pathfinding of two unique repetitive families.

摘要

通过从小麦基因组中分离这些元件的小片段,有效地鉴定了新的重复 DNA 元件类别。利用 Triticum monococcum 构建了一个小麦 A 基因组文库,通过 EcoO109I 进行退化切割,其识别位点由 5'-PuGGNCCPy-3'多序列组成。筛选并通过印迹法测试了三个来自 A 基因组的新重复序列 pTm6、pTm69 和 pTm58 的高拷贝数。pTm6 与大麦 Ty1-Copia-retrotransposon BARE-1 的整合酶结构域具有同源性,pTm58 与大麦 Ty3-gypsy-like retrotransposon Romani 具有相似性。然而,pTm69 构成了串联阵列,具有有用的基因组特异性,但与已知的重复元件没有任何同一性。本研究还试图通过基因组消减分离小麦 D 基因组特异性重复元件,而不考虑甲基化水平。用甲基化不敏感的 4 bp 切割器 MboI 将 Aegilops tauschii 的总基因组 DNA 切成小片段,然后用过量的 T. turgidum 基因组 DNA 退火,从 Ae. tauschii 和 Triticum turgidum 之间减去常见的 DNA 序列。分离出 D 基因组重复序列 pAt1,并用于从小麦细菌人工染色体中鉴定出一个额外的新型重复序列家族,其大小范围为 1 395-1 850 bp。这些方法成功地为两个独特的重复家族的探索提供了线索。

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