脱氧核糖核酸
生物
DNA复制
细胞周期
抄写(语言学)
DNA
细胞生物学
复制的起源
原点识别复合体
细胞
细胞生长
分子生物学
遗传学
真核细胞DNA复制
语言学
哲学
作者
Judith W. Zyskind,Douglas W. Smith
出处
期刊:Cell
[Cell Press]
日期:1992-04-01
卷期号:69 (1): 5-8
被引量:90
标识
DOI:10.1016/0092-8674(92)90112-p
摘要
The coupling of replication to the cell cycle and cell growth involves events that occur at oriC. Immediately after initiation, there is an eclipse phase during which reinitiation from the newly synthesized origins is prevented. GATC sites in oriC remain in a hemimethylated state longer than other sites because of their association with the outer membrane, which prevents DnaA from binding and activating additional rounds of initiation. After the origins are methylated and released from the outer membrane, the concentration of newly synthesized DnaA and the activation of oriC by transcription from the nearby mioC and gid promoters determine when the next rounds of replication initiate. If growth rate is reduced, the synthesis of (p)ppGpp will increase, and this will lead to a decrease in dnaA, mioC, and gid transcription. On the other hand, if growth rate is increased by access to a tasty meal, synthesis of (p)ppGpp will decrease, expression of dnaA, mioC, and gid genes will increase, and a shortening of the interinitiation time will result. The participation of all these control features ensures rapid and precise coordination of DNA replication with cell growth.
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