首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >In vivo evidence for the involvement of anionic phospholipids in initiation of DNA replication in Escherichia coli.
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In vivo evidence for the involvement of anionic phospholipids in initiation of DNA replication in Escherichia coli.

机译:在大肠杆菌中,阴离子磷脂参与DNA复制的起始的体内证据。

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摘要

In vitro, anionic phospholipids can reactivate inactivated DnaA protein, which is essential for initiation of DNA replication at the oriC site of Escherichia coli [Sekimizu, K. & Kornberg, A. (1988) J. Biol. Chem. 263, 7131-7135]. Mutations in the pgsA gene (encoding phosphatidylglycerophosphate synthase) limit the synthesis of the major anionic phospholipids and lead to arrest of cell growth. We report herein that a mutation in the rnhA gene (encoding RNase H) that bypasses the need for the DnaA protein through induction of constitutive stable DNA replication [Kogoma, T. & von Meyenburg, K. (1983) EMBO J. 2, 463-468] also suppressed the growth arrest phenotype of a pgsA mutant. The maintenance of plasmids dependent on an oriC site for replication, and therefore DnaA protein, was also compromised under conditions of limiting anionic phospholipid synthesis. These results provide support for the involvement of anionic phospholipids in normal initiation of DNA replication at oriC in vivo by the DnaA protein.
机译:在体外,阴离子磷脂可以使失活的DnaA蛋白重新活化,这对于在大肠杆菌的oriC位点启动DNA复制是必不可少的[Sekimizu,K.&Kornberg,A.(1988)J.化学263,7131-7135]。 pgsA基因(编码磷脂酰甘油磷酸合酶)中的突变限制了主要阴离子磷脂的合成,并导致细胞生长停滞。我们在此报告,rnhA基因突变(编码RNase H),通过诱导组成型稳定DNA复制而绕过DnaA蛋白的需要[Kogoma,T.&von Meyenburg,K.(1983)EMBO J. 2,463 -468]也抑制了pgsA突变体的生长停滞表型。在限制阴离子磷脂合成的条件下,取决于复制的oriC位点的质粒的维持,以及因此DnaA蛋白的维持也受到损害。这些结果为阴离子磷脂参与DnaA蛋白在oriC体内DNA复制正常启动中提供了支持。

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