Comparison of Transcription Elongation Rates of Three RNA Polymerases in Real Time

被引:0
|
作者
Tare, Priyanka [1 ]
Bhowmick, Tuhin [2 ,3 ]
Katagi, Gurunath [3 ]
China, Arnab [1 ]
Nagaraja, Valakunja [1 ]
机构
[1] Indian Inst Sci, Dept Microbiol & Cell Biol, Bangalore 560012, India
[2] Indian Inst Sci, Dept Phys, Bangalore 560012, India
[3] Pandorum Technol Pvt Ltd, Ctr Cellular & Mol Platforms, NCBS TIFR, Bangalore 560065, India
来源
ACS OMEGA | 2023年 / 8卷 / 50期
关键词
ESCHERICHIA-COLI; MYCOBACTERIUM-TUBERCULOSIS; SINGLE-MOLECULE; TERMINATION; PATHWAY; GROWTH; GENES; FORCE; INITIATION; BINDING;
D O I
10.1021/acsomega.3c04754
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
RNA polymerases (RNAPs) across the bacterial kingdom have retained a conserved structure and function. In spite of the remarkable similarity of the enzyme in different bacteria, a wide variation is found in the promoter-polymerase interaction, transcription initiation, and termination. However, the transcription elongation was considered to be a monotonic process, although the rate of elongation could vary in different bacteria. Such variations in RNAP elongation rates could be important to fine-tune the transcription, which in turn would influence cellular metabolism and growth rates. Here, we describe a quantitative study to measure the transcription rates for the RNAPs from three bacteria, namely, Mycobacterium tuberculosis, Mycobacterium smegmatis, and Escherichia coli, which exhibit different growth kinetics. The RNA synthesis rates of the RNAPs were calculated from the real-time elongation kinetic profile using surface plasmon resonance through a computational flux flow model. The computational model revealed the modular process of elongation, with different rate profiles for the three RNAPs. Notably, the transcription elongation rates of these RNAPs followed the trend in the growth rates of these bacteria.
引用
收藏
页码:47510 / 47519
页数:10
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