Epstein C B, Cross F R
Rockefeller University, New York, New York 10021.
Mol Cell Biol. 1994 Mar;14(3):2041-7. doi: 10.1128/mcb.14.3.2041-2047.1994.
Cell cycle START in Saccharomyces cerevisiae requires at least one of the three CLN genes (CLN1, CLN2, or CLN3). A total of 12 mutations bypassing this requirement were found to be dominant mutations in a single gene that we named BYC1 (for bypass of CLN requirement). We also isolated a plasmid that had cln bypass activity at a low copy number; the gene responsible was distinct from BYC1 and was identical to the recently described BCK2 gene. Strains carrying bck2::ARG4 disruption alleles were fully viable, but bck2::ARG4 completely suppressed the cln bypass activity of BYC1. swi4 and swi6 deletion alleles also efficiently suppressed BYC1 cln bypass activity; Swi4 and Swi6 are components of a transcription factor previously implicated in control of CLN1 and CLN2 expression. bck2::ARG4 was synthetically lethal with cln3 deletion, suggesting that CLN1 and CLN2 cannot function in the simultaneous absence of BCK2 and CLN3; this observation correlates with low expression of CLN1 and CLN2 in bck2 strains deprived of CLN3 function. Thus, factors implicated in CLN1 and CLN2 expression and/or function are also required for BYC1 function in the absence of all three CLN genes; this may suggest the involvement of other targets of Swi4, Swi6, and Bck2 in START.
酿酒酵母中的细胞周期起始需要三个CLN基因(CLN1、CLN2或CLN3)中的至少一个。总共发现12个绕过这一需求的突变是一个单一基因中的显性突变,我们将该基因命名为BYC1(用于绕过CLN需求)。我们还分离出了一个在低拷贝数时具有cln绕过活性的质粒;负责的基因与BYC1不同,与最近描述的BCK2基因相同。携带bck2::ARG4破坏等位基因的菌株完全可存活,但bck2::ARG4完全抑制了BYC1的cln绕过活性。swi4和swi6缺失等位基因也有效地抑制了BYC1的cln绕过活性;Swi4和Swi6是一种转录因子的组成部分,该转录因子先前与CLN1和CLN2的表达调控有关。bck2::ARG4与cln3缺失是合成致死的,这表明在同时缺失BCK2和CLN3的情况下,CLN1和CLN2无法发挥功能;这一观察结果与在缺乏CLN3功能的bck2菌株中CLN1和CLN2的低表达相关。因此,在所有三个CLN基因均缺失的情况下,BYC1发挥功能也需要与CLN1和CLN2表达和/或功能相关的因子;这可能表明Swi4、Swi6和Bck2的其他靶点也参与了起始过程。