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Construction of a BAC library of Physcomitrella patens and isolation of a LEA gene

机译:枯草小肠杆菌BAC文库的构建及LEA基因的分离

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The moss Physcomitrella patens is an ideal model system for the study of plant physiology and developmental biology. The evolutionary position of moss makes P. patens an ideal subject for the study of land plant evolution. Furthermore, as P. patens is highly tolerant to drought, salt and freezing, it may contain important resistant gene resources. For these reasons, a bacterial artificial chromosome (BAC) library of P patens was constructed. The high molecular weight (HMW) DNA was partially digested with HindIII. One size fractionation was carried out by pulsed field gel electrophoresis (PFGE) and the selected fragments were ligated to the vector pGUGIBAC1. The ligation mixture was transformed into DH10B cells and recombinants were picked out. In total, 49,920 BAC clones were collected. The BAC library has an average insert size of 65 kb and about seven-fold genome coverage. The hybridization results probed by chloroplast and mitochondrial genes demonstrated that the BAC library has no significant organellar DNA contaminations. The BAC clones were stored using two methods: one involved storing the library in 384-well plates, 1 clone in 1 well; in the other, the library was stored in 96-well plates, 12 clones being pooled together into well. Late embryogenesis-abundant (LEA) proteins are thought to act as a protective component in respond to dehydration, osmotic, and low-temperature stresses. The BAC library was screened with a LEA gene as a probe using rapid PCR methods and six positive clones were screened Out. The constructed BAC library will be useful for gene screening and cloning of P patens. In addition, this BAC library provides a valuable tool for the genomic study of P patens. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
机译:苔藓小藓是研究植物生理学和发育生物学的理想模型系统。苔藓的进化位置使P. patens成为研究陆地植物进化的理想学科。此外,由于彭氏疟原虫对干旱,盐和冻结具有高度的耐受性,因此它可能含有重要的抗性基因资源。由于这些原因,构建了细菌的细菌人工染色体(BAC)文库。高分子量(HMW)DNA用HindIII部分消化。通过脉冲场凝胶电泳(PFGE)进行一种大小分级分离,并将选定的片段连接到载体pGUGIBAC1。将连接混合物转化为DH10B细胞,并挑选重组体。总共收集了49,920个BAC克隆。 BAC文库的平均插入片段大小为65 kb,基因组覆盖率约为7倍。叶绿体和线粒体基因的杂交结果表明,BAC文库没有明显的细胞器DNA污染。 BAC克隆的存储方法有两种:一种是将文库存储在384孔板中,一种是将克隆存储在1孔中。在另一种方法中,该文库存储在96孔板中,将12个克隆一起汇集到孔中。人们认为晚期胚胎发生丰富(LEA)蛋白在响应脱水,渗透和低温胁迫时起保护作用。使用快速PCR方法以LEA基因为探针筛选BAC文库,并筛选出六个阳性克隆。构建的BAC文库可用于基因筛选和克隆。此外,该BAC库为P染色体的基因组研究提供了有价值的工具。 (C)2004 Elsevier Ireland Ltd.保留所有权利。

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