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基于修正核苷酸序列的插入元件IS2的基因组织。

Genetic organization of insertion element IS2 based on a revised nucleotide sequence.

作者信息

Ronecker H J, Rak B

机构信息

Institut für Biologie III, Universität, Freiburg, F.R.G.

出版信息

Gene. 1987;59(2-3):291-6. doi: 10.1016/0378-1119(87)90337-4.

Abstract

We identified a transposable element resident in the chromosome of Escherichia coli K-12 strain HB101. This is an approx. 4400-bp-long transposon flanked by two copies of insertion sequence (IS) 1 element in direct orientation. One of the IS1 elements was found to be integrated into an IS2 element between IS2 bp 139 and bp 140 with the large moiety of IS2 within the transposon. The sequence of this part of IS2 differs from the published sequence of galOP-308::IS2 at a number of positions. Restriction analysis of the published allele, however, indicated that both alleles may in fact be identical. Since six of the eight differences found alter open reading frames, the revised sequence presents a new outlook for the potential genetic organization of IS2.

摘要

我们在大肠杆菌K-12菌株HB101的染色体中鉴定出一种转座元件。这是一个约4400 bp长的转座子,两侧是两个同向排列的插入序列(IS)1元件。其中一个IS1元件被发现整合到IS2元件中,位于IS2的139 bp和140 bp之间,且转座子内有大部分IS2。IS2这部分的序列在多个位置与已发表的galOP-308::IS2序列不同。然而,对已发表等位基因的限制性分析表明,这两个等位基因实际上可能是相同的。由于发现的八个差异中有六个改变了开放阅读框,因此修订后的序列为IS2的潜在遗传组织提供了新的视角。

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