Ireton K, Grossman A D
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
EMBO J. 1994 Apr 1;13(7):1566-73. doi: 10.1002/j.1460-2075.1994.tb06419.x.
Spore formation in Bacillus subtilis requires the generation of two distinct cell types, each with an active chromosome that becomes committed to a defined program of gene expression. Here we show that a developmental checkpoint couples the initiation of sporulation, and the subsequent formation of these two cell types, to DNA replication early during development. Inhibiting the initiation of chromosomal replication prevents the onset of sporulation and inhibits expression of several genes that are normally induced early during development. This defect in gene expression is due to inhibition of the multi-component phosphorylation pathway needed to activate the developmental transcription factor encoded by spo0A. The target affected by inhibiting the initiation of replication is neither Spo0A nor the major kinase, KinA, needed for production of Spo0A approximately P. Rather, the target appears to be one of the proteins that transfers phosphate from the kinase to the Spo0A transcription factor. The signal that couples activity of the phosphorelay to the initiation of DNA replication is different from the previously described DNA damage signal that inhibits the phosphorelay during SOS induction in a recA-dependent response. Thus, DNA replication as well as DNA damage signals control production of Spo0A approximately P and initiation of sporulation.
枯草芽孢杆菌中的芽孢形成需要产生两种不同的细胞类型,每种细胞类型都有一条活跃的染色体,该染色体致力于特定的基因表达程序。在这里,我们表明,一个发育检查点将芽孢形成的起始以及随后这两种细胞类型的形成与发育早期的DNA复制联系起来。抑制染色体复制的起始会阻止芽孢形成的开始,并抑制一些通常在发育早期被诱导表达的基因的表达。这种基因表达缺陷是由于抑制了激活由spo0A编码的发育转录因子所需的多组分磷酸化途径。抑制复制起始所影响的靶点既不是Spo0A,也不是产生磷酸化Spo0A(Spo0AP)所需的主要激酶KinA。相反,靶点似乎是将磷酸从激酶转移到Spo0A转录因子的蛋白质之一。将磷酸传递体的活性与DNA复制起始联系起来的信号不同于先前描述的在SOS诱导期间以recA依赖反应抑制磷酸传递体的DNA损伤信号。因此,DNA复制以及DNA损伤信号控制着磷酸化Spo0A(Spo0AP)的产生和芽孢形成的起始。