Schubert Rachel A, Dodd Ian B, Egan J Barry, Shearwin Keith E
Molecular and Biomedical Sciences (Biochemistry), University of Adelaide, Adelaide, SA 5005, Australia.
Genes Dev. 2007 Oct 1;21(19):2461-72. doi: 10.1101/gad.1584907.
CI represses cro; Cro represses cI. This double negative feedback loop is the core of the classical CI-Cro epigenetic switch of bacteriophage lambda. Despite the classical status of this switch, the role in lambda development of Cro repression of the P(RM) promoter for CI has remained unclear. To address this, we created binding site mutations that strongly impaired Cro repression of P(RM) with only minimal effects on CI regulation of P(RM). These mutations had little impact on lambda development after infection but strongly inhibited the transition from lysogeny to the lytic pathway. We demonstrate that following inactivation of CI by ultraviolet treatment of lysogens, repression of P(RM) by Cro is needed to prevent synthesis of new CI that would otherwise significantly impede lytic development. Thus a bistable CI-Cro circuit reinforces the commitment to a developmental transition.
CI抑制cro;Cro抑制cI。这种双重负反馈回路是噬菌体λ经典的CI-Cro表观遗传开关的核心。尽管这个开关具有经典地位,但Cro对CI的P(RM)启动子的抑制在λ发育中的作用仍不清楚。为了解决这个问题,我们创建了结合位点突变,这些突变强烈损害了Cro对P(RM)的抑制,而对CI对P(RM)的调控影响最小。这些突变在感染后对λ发育影响很小,但强烈抑制了从溶原状态到裂解途径的转变。我们证明,在用紫外线处理溶原菌使CI失活后,需要Cro对P(RM)的抑制来防止新的CI合成,否则会严重阻碍裂解发育。因此,一个双稳态的CI-Cro回路强化了对发育转变的承诺。