Sturm S, Okayama H
Okayama Cell Switching Project, Research Development Corporation of Japan, Kyoto, Japan.
Mol Biol Cell. 1996 Dec;7(12):1967-76. doi: 10.1091/mbc.7.12.1967.
In Schizosaccharomyces pombe the "start" of the cell cycle is regulated by two parallel, functionally overlapping complexes composed of Res1-Cdc10 and Res2-Cdc10. Res1 and Res2 are structurally very homologous and are required for the start of the mitotic and meiotic cycle, respectively. We have addressed the question which parts of the proteins are essential for function and determine the functional specificity. Several discrete domains in the nonconserved C-terminal region are essential for the mitotic and meiotic start function and determine the functional specificity independently of the structurally conserved motifs at the N-terminal end and in the center. One of these domains in Res2 restricts Res2 to interact only with Rep2. Res2 without this domain behaves like a functional chimera having the properties of Res2 and Res1. Likewise, internally truncated forms of Res1 lacking the centrally located ankyrin repeats and adjacent sequences can partially suppress the meiotic defect in res2- cells. These truncated Res1 molecules behave like functional chimeras with the properties of Res1 and Res2.
在粟酒裂殖酵母中,细胞周期的“起始”由两个平行的、功能重叠的复合物调控,这两个复合物分别由Res1-Cdc10和Res2-Cdc10组成。Res1和Res2在结构上非常同源,分别是有丝分裂和减数分裂周期起始所必需的。我们探讨了蛋白质的哪些部分对功能至关重要,并确定了功能特异性。非保守C末端区域中的几个离散结构域对于有丝分裂和减数分裂起始功能至关重要,并且独立于N末端和中心的结构保守基序来确定功能特异性。Res2中的这些结构域之一限制Res2仅与Rep2相互作用。没有这个结构域的Res2表现得像一个具有Res2和Res1特性的功能性嵌合体。同样,缺少位于中心位置的锚蛋白重复序列和相邻序列的Res1内部截短形式可以部分抑制res2-细胞中的减数分裂缺陷。这些截短的Res1分子表现得像具有Res1和Res2特性的功能性嵌合体。