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细菌中的转录偶联类核结构

Transcription-coupled nucleoid architecture in bacteria.

作者信息

Ohniwa Ryosuke L, Morikawa Kazuya, Takeshita Sayaka L, Kim Joongbaek, Ohta Toshiko, Wada Chieko, Takeyasu Kunio

机构信息

Laboratory of Plasma Membrane and Nuclear Signaling, Kyoto University, Graduate School of Biostudies, Yoshidahonmachi, Sakyo-ku, Kyoto 606-8501, Japan.

出版信息

Genes Cells. 2007 Oct;12(10):1141-52. doi: 10.1111/j.1365-2443.2007.01125.x.

Abstract

The circular bacterial genome DNA exists in cells in the form of nucleoids. In the present study, using genetic, molecular and structural biology techniques, we show that nascent single-stranded RNAs are involved in the step-wise folding of nucleoid fibers. In Escherichia coli, RNase A degraded thicker fibers (30 and 80 nm wide) into thinner fibers (10 nm wide), while RNase III and RNase H degraded 80-nm fibers into 30-nm (but not 10-nm) fibers. Similarly in Staphylococcus aureus, RNase A treatment resulted in 10-nm fibers. Treatment with the transcription inhibitor, rifampicin, in the absence of RNase A changed most nucleoid fibers to 10-nm fibers. Proteinase-K treatment of nucleoids exposed DNA. Thus, the smallest structural unit is an RNase A-resistant 10-nm fiber composed of DNA and proteins, and the hierarchical structure of the bacterial chromosome is controlled by transcription itself. In addition, the formation of 80-nm fibers from 30-nm fibers requires double-stranded RNA and RNA-DNA hetero duplex. RNA is evident in the architecture of log-phase uncondensed and stationary-phase condensed nucleoids.

摘要

环状细菌基因组DNA以类核的形式存在于细胞中。在本研究中,我们运用遗传学、分子生物学和结构生物学技术表明,新生单链RNA参与类核纤维的逐步折叠。在大肠杆菌中,核糖核酸酶A将较粗的纤维(30纳米和80纳米宽)降解为较细的纤维(10纳米宽),而核糖核酸酶III和核糖核酸酶H将80纳米的纤维降解为30纳米(而非10纳米)的纤维。同样,在金黄色葡萄球菌中,核糖核酸酶A处理产生10纳米的纤维。在不存在核糖核酸酶A的情况下,用转录抑制剂利福平处理会使大多数类核纤维变为10纳米的纤维。用蛋白酶K处理类核会使DNA暴露。因此,最小的结构单元是由DNA和蛋白质组成的抗核糖核酸酶A的10纳米纤维,细菌染色体的层次结构由转录本身控制。此外,从30纳米纤维形成80纳米纤维需要双链RNA和RNA-DNA异源双链体。RNA在对数期未浓缩和稳定期浓缩类核的结构中很明显。

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