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大麦(Hordeum vulgare L.)酵母人工染色体文库的构建及Hor1特异性克隆的分离。

Construction of a barley (Hordeum vulgare L.) YAC library and isolation of a Hor1-specific clone.

作者信息

Kleine M, Michalek W, Graner A, Herrmann R G, Jung C

机构信息

Botanisches Institut der Ludwig-Maximilians-Universität München, Germany.

出版信息

Mol Gen Genet. 1993 Aug;240(2):265-72. doi: 10.1007/BF00277065.

Abstract

We have constructed an EcoRI-based YAC (yeast artificial chromosome) library from barley (Hordeum vulgare L. cv. Franka) using the vector pYAC4. The library consists of approximately 18,000 recombinant YACs with insert sizes ranging between 100 and 1000 kb (average of 160 kb) corresponding to 50% of the barley genome. Size fractionation after ligation resulted in an increased average insert size (av. 370 kb) but also in a substantial decrease in cloning efficiency. Less than 1% of the colonies showed homology to a plastome-specific probe; approximately 50% of the colonies displayed a signal with a dispersed, highly repetitive barley-specific probe. Using a primer combination deduced from the sequence of a member of the small Hor1 gene family coding for the C-hordein storage proteins, the library was screened by polymerase chain reaction and subsequently by the colony hybridization technique. A single YAC, designated Y66C11, with a 120 kb insert was isolated. This DNA fragment represents a coherent stretch from the terminal part of the Hor1 gene region as judged from the correspondence of the restriction patterns between Y66C11 DNA and barley DNA after hybridization with the Hor1-specific probe. Restriction with the isoschizomeric enzymes HpaII/MspI suggests a high degree of methylation of the Hor1 region in mesophyll cells but not in YAC-derived (yeast) DNA.

摘要

我们使用载体pYAC4构建了一个基于EcoRI的大麦(Hordeum vulgare L. cv. Franka)酵母人工染色体(YAC)文库。该文库由大约18,000个重组YAC组成,插入片段大小在100至1000 kb之间(平均160 kb),相当于大麦基因组的50%。连接后的大小分级导致平均插入片段大小增加(平均370 kb),但克隆效率大幅降低。不到1%的菌落与质体基因组特异性探针显示出同源性;大约50%的菌落与分散的、高度重复的大麦特异性探针产生信号。使用从小Hor1基因家族中编码C-大麦醇溶蛋白储存蛋白的一个成员的序列推导而来的引物组合,通过聚合酶链反应随后通过菌落杂交技术对文库进行筛选。分离出了一个单一的YAC,命名为Y66C11,其插入片段为120 kb。从Y66C11 DNA与大麦DNA在与Hor1特异性探针杂交后的限制性图谱的对应关系判断,该DNA片段代表了Hor1基因区域末端部分的一段连贯序列。用同裂酶HpaII/MspI进行酶切表明,Hor1区域在叶肉细胞中高度甲基化,但在YAC衍生的(酵母)DNA中并非如此。

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