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[生绿链霉菌ATCC27422染色体复制起点(oriC)的序列与功能分析]

[Sequence and functional analysis of the chromosome replication origin (oriC) of Streptoverticillum caespitosus ATCC27422].

作者信息

Ma Wei, Mao Xiang, Lu Jie, Jiang Wei-Hong, Qin Zhong-Jun, Zhao Guo-Ping

机构信息

Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, the Chinese Academy of Sciences, Shanghai 200032, China.

出版信息

Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2003 Oct;35(10):930-6.

Abstract

Twenty-two DnaA boxes were identified in the chromosome replication origin (oriC) of Streptoverticillum caespitosus ATCC27422 based upon the characteristics of consensus sequences. The 21st and 22nd DnaA boxes overlapped 8 base pairs each other reversely. Compared with the oriC database of actinomycetes, similar overlapping DnaA boxes were recognized in several species of Streptomyces and Mycobacterium. These overlapping DnaA boxes were composed of the last two DnaA box (21st and 22nd) in the Streptomyces species, but the of 1st and 2nd ones in the Mycobacterium species. The consensus sequence of the overlapping DnaA box is CTGTGCACAA, one base longer than the normal DnaA box sequence presumably due to the overlapping structure. Although the DnaA boxes exist in the 189 792 bp region only, the 1 188 bp and 793 939 bp regions are also important to the DNA replication. Deletion of the 1 188 bp region may cause absolute loss of DNA replication initiation activity measured by the transformation efficiency of plasmids with truncated oriC. When the 793 939 bp region was truncated, the transformation efficiency reduced about 40%. If the oriC was cloned into a vector with partial flanking region sequences (partial dnaA and dnaN gene sequences), the transformation rate was about 4.3-fold lower than that of the construct containing the oriC region only. However, the transformants were much more similar to the host with respect to the morphology of colony and mycelium. The cis-regulatory functions of the flanking sequences, which may influence the initiation efficiency of the chromosome replication and/or the stability of replicon, are thus suggested.

摘要

基于共有序列的特征,在生二素链霉菌ATCC27422的染色体复制起点(oriC)中鉴定出22个DnaA框。第21个和第22个DnaA框彼此反向重叠8个碱基对。与放线菌的oriC数据库相比,在几种链霉菌属和分枝杆菌属物种中识别出了类似的重叠DnaA框。这些重叠的DnaA框由链霉菌属物种中的最后两个DnaA框(第21个和第22个)组成,但在分枝杆菌属物种中是第1个和第2个。重叠DnaA框的共有序列是CTGTGCACAA,比正常的DnaA框序列长一个碱基,可能是由于重叠结构所致。尽管DnaA框仅存在于189792 bp区域,但1188 bp和793939 bp区域对DNA复制也很重要。删除1188 bp区域可能会导致通过截短oriC的质粒转化效率来衡量的DNA复制起始活性完全丧失。当793939 bp区域被截短时,转化效率降低约40%。如果将oriC克隆到带有部分侧翼区域序列(部分dnaA和dnaN基因序列)的载体中,转化率比仅包含oriC区域的构建体低约4.3倍。然而,就菌落和菌丝体的形态而言,转化体与宿主更为相似。因此表明了侧翼序列的顺式调节功能,其可能影响染色体复制的起始效率和/或复制子的稳定性。

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