Purnapatre Kedar, Piccirillo Sarah, Schneider Brandt L, Honigberg Saul M
Division of Cell Biology and Biophysics, School of Biological Sciences, University of Missouri-Kansas City, Kansas City, MO 64110-2499, USA.
Genes Cells. 2002 Jul;7(7):675-91. doi: 10.1046/j.1365-2443.2002.00551.x.
IME1, which is required for the initiation of meiosis, is regulated by Cln3:Cdc28 kinase, which activates the G1-to-S transition, and Snf1 kinase, which mediates glucose repression. Here we examine the pathway by which Cln3:Cdc28p represses IME1 and the relationship between Cln3:Cdc28p and Snf1p in this regulation.
When wild-type yeast cease growth, they express IME1 to moderate levels, intermediate between the low levels expressed during growth and the high levels expressed during sporulation. Moderate IME1 expression occurred in cln3Delta, cln1Delta cln2Delta, cdc28-4 and swi6Delta mutants, even during growth. These mutants also induced IME1 expression more rapidly than the wild-type. CLN3 required SWI6 and CLN2 to repress IME1 and IME2, but CLN1 was much less active than CLN2 in this repression. The phenotype of the cln3Delta snf1Delta double mutant indicated that Cln3:Cdc28p regulates IME1 independently of SNF1.
Entry into meiosis involves two independent but sequential controls, which regulate IME1 via a three position switch: (i) during growth IME1 is repressed by the CLN3/SWI6/CLN2 pathway, (ii) once growth ceases, this repression is released and IME1 is expressed at moderate levels, and (iii) subsequently, nutritional conditions that activate Snf1p allow high IME1 expression.
减数分裂起始所需的IME1受Cln3:Cdc28激酶调控,该激酶激活G1期到S期的转换,以及Snf1激酶,其介导葡萄糖阻遏。在此我们研究Cln3:Cdc28p抑制IME1的途径以及在此调控中Cln3:Cdc28p与Snf1p之间的关系。
当野生型酵母停止生长时,它们将IME1表达至中等水平,介于生长期间表达的低水平和孢子形成期间表达的高水平之间。即使在生长期间,cln3Δ、cln1Δ cln2Δ、cdc28 - 4和swi6Δ突变体中也出现中等水平的IME1表达。这些突变体诱导IME1表达的速度也比野生型更快。CLN3需要SWI6和CLN2来抑制IME1和IME2,但在这种抑制中CLN1的活性远低于CLN2。cln3Δ snf1Δ双突变体的表型表明Cln3:Cdc28p独立于SNF1调控IME1。
进入减数分裂涉及两个独立但相继的控制,它们通过一个三位开关调控IME1:(i) 在生长期间IME1被CLN3/SWI6/CLN2途径抑制,(ii) 一旦生长停止,这种抑制被解除且IME1以中等水平表达,以及(iii) 随后,激活Snf1p的营养条件允许IME1高表达。