化学
机制(生物学)
核苷酸
聚合酶
动能
RNA聚合酶
核糖核酸
生物化学
计算生物学
生物物理学
分子生物学
酶
基因
物理
量子力学
生物
作者
Kaila B. Fuller,Ruth Q. Jacobs,Zachariah I. Carter,Zachary G. Cuny,David A. Schneider,Aaron L. Lucius
标识
DOI:10.1016/j.bpc.2024.107281
摘要
RNA polymerase I (Pol I) is responsible for synthesizing ribosomal RNA, which is the rate limiting step in ribosome biogenesis. We have reported wide variability in the magnitude of the rate constants defining the rate limiting step in sequential nucleotide additions catalyzed by Pol I. in this study we sought to determine if base identity impacts the rate limiting step of nucleotide addition catalyzed by Pol I. To this end, we report a transient state kinetic interrogation of AMP, CMP, GMP, and UMP incorporations catalyzed by Pol I. We found that Pol I uses one kinetic mechanism to incorporate all nucleotides. However, we found that UMP incorporation is faster than AMP, CMP, and GMP additions. Further, we found that endonucleolytic removal of a dimer from the 3′ end was fastest when the 3′ terminal base is a UMP. It has been previously shown that both downstream and upstream template sequence identity impacts the kinetics of nucleotide addition. The results reported here show that the incoming base identity also impacts the magnitude of the observed rate limiting step.
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