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由微型γδ(Tn1000)转座子产生的倒位和缺失。

Inversions and deletions generated by a mini-gamma delta (Tn1000) transposon.

作者信息

Wang G, Xu X, Chen J M, Berg D E, Berg C M

机构信息

Department of Molecular and Cell Biology, University of Connecticut, Storrs 06269-2131.

出版信息

J Bacteriol. 1994 Mar;176(5):1332-8. doi: 10.1128/jb.176.5.1332-1338.1994.

Abstract

Intramolecular transposition by an engineered derivative of the transposon gamma delta (Tn1000) is described. This 1-kb element contains inverted repeats of the 40 bp of the delta end of gamma delta, bracketing a kan gene, but it contains no resolution site. Transposition was analyzed in two plasmids; one contained two contraselectable (conditional lethal) genes (thyA and sacB) adjacent to the mini-gamma delta element in a 13.0-kb pBR322/pUC-based two-component plasmid (a heterodimer), and the other contained a different contraselectable gene (strA [rpsL]) in a 13.2-kb three-component plasmid (a heterotrimer). Selection for loss of function of a single contraselectable gene yielded inversions and deletions. Each inversion plasmid was 1 kb larger than the parent plasmid: it had a second copy of mini-gamma delta inserted in the contraselected gene, with that copy plus the intervening segment inverted, and the 5-bp target site duplicated. Each deletion plasmid was smaller than the parent plasmid and had a deletion that extended from one transposon end into or through the contraselected gene for distances of up to 9.4 kb. The frequencies of deletions versus inversions ending in a single target gene were similar, although overall, deletions outnumbered inversions because deletions, but not inversions, into sites beyond the contraselected gene inactivate it. This work also demonstrates that thyA (which encodes thymidylate synthetase) is a useful contraselectable marker.

摘要

描述了转座子γδ(Tn1000)的一种工程衍生物的分子内转座。这个1千碱基对的元件包含γδ末端40碱基对的反向重复序列,两侧是一个卡那霉素基因,但它不含解离位点。在两种质粒中分析了转座情况;一种是在基于13.0千碱基对的pBR322/pUC的双组分质粒(异二聚体)中,迷你γδ元件旁边有两个反选择(条件致死)基因(thyA和sacB);另一种是在13.2千碱基对的三组分质粒(异三聚体)中含有一个不同的反选择基因(strA [rpsL])。对单个反选择基因功能丧失的选择产生了倒位和缺失。每个倒位质粒比亲本质粒大1千碱基对:它在反选择基因中插入了迷你γδ的第二个拷贝,该拷贝加上中间片段发生了倒位,并且5碱基对的靶位点重复。每个缺失质粒比亲本质粒小,并且有一个缺失,其从一个转座子末端延伸到反选择基因中或穿过该基因,长度可达9.4千碱基对。以单个靶基因结束的缺失与倒位的频率相似,尽管总体上缺失比倒位多,因为进入反选择基因之外位点的缺失会使其失活,而倒位不会。这项工作还表明thyA(编码胸苷酸合成酶)是一个有用的反选择标记。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d091/205197/da0efe0b8350/jbacter00023-0140-a.jpg

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