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参与流感嗜血杆菌Rd转化的一组基因的核苷酸序列

Nucleotide sequence of a cluster of genes involved in the transformation of Haemophilus influenzae Rd.

作者信息

Tomb J F, el-Hajj H, Smith H O

机构信息

Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2185.

出版信息

Gene. 1991 Jul 31;104(1):1-10. doi: 10.1016/0378-1119(91)90457-m.

Abstract

A genetic locus implicated in the development of competence in Haemophilus influenzae Rd has been previously mapped to a 12.8-kb PstI region of the chromosome [Tomb et al., J. Bacteriol. 171 (1989) 3796-3802]. To define the boundaries of this locus and to identify the gene(s) involved in transformation, additional mini-Tn10kan mutagenesis was performed and the region containing all mutagenic insertions was sequenced. Three new transformation-deficient (Tfo-) mutants were found, bringing the number of distinct mutations mapped to this region up to eight. The transformation frequency of strains carrying the new insertions was 25- to 10(5)-fold less than wild type. The ends of the mini-Tn10kan element were used as starting points to sequence a 9.1-kb region. The position of the eight mutagenic insertions was determined and ten putative open reading frames (ORFs) were found. One of the mini-Tn10kan elements had inserted in an intergenic region while the rest had inserted in six of the ORFs. Based on the phenotypes of the mutant strains and the position of the insertions, we concluded that at least three of the genes should be involved in transformation. In addition, fourteen 9-11-bp uptake signal sequences (USS) were found, four of which were part of stem-loop structures and could function as attenuators of terminators of transcription.

摘要

一个与流感嗜血杆菌Rd感受态发育相关的基因座先前已被定位到染色体上一个12.8 kb的PstI区域[Tomb等人,《细菌学杂志》171(1989)3796 - 3802]。为了确定该基因座的边界并鉴定参与转化的基因,进行了额外的mini-Tn10kan诱变,并对包含所有诱变插入片段的区域进行了测序。发现了三个新的转化缺陷型(Tfo-)突变体,使定位到该区域的不同突变数量增加到八个。携带新插入片段的菌株的转化频率比野生型低25至10^5倍。以mini-Tn10kan元件的末端为起点,对一个9.1 kb的区域进行了测序。确定了八个诱变插入片段的位置,并发现了十个推定的开放阅读框(ORF)。其中一个mini-Tn10kan元件插入到一个基因间区域,其余的插入到六个ORF中。根据突变菌株的表型和插入片段的位置,我们得出结论,至少有三个基因参与转化。此外,还发现了14个9 - 11 bp的摄取信号序列(USS),其中四个是茎环结构的一部分,可以作为转录终止子的衰减子发挥作用。

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