McDonald Christine M, Cooper Katrina F, Winter Edward
Department of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, Pennsylvania 19102, USA.
Genetics. 2005 Nov;171(3):901-11. doi: 10.1534/genetics.105.045567. Epub 2005 Aug 3.
Smk1 is a meiosis-specific MAPK homolog in Saccharomyces cerevisiae that regulates the postmeiotic program of spore formation. Similar to other MAPKs, it is activated via phosphorylation of the T-X-Y motif in its regulatory loop, but the signals controlling Smk1 activation have not been defined. Here we show that Ama1, a meiosis-specific activator of the anaphase-promoting complex/cyclosome (APC/C), promotes Smk1 activation during meiosis. A weakened allele of CDC28 suppresses the sporulation defect of an ama1 null strain and increases the activation state of Smk1. The function of Ama1 in regulating Smk1 is independent of the FEAR network, which promotes exit from mitosis and exit from meiosis I through the Cdc14 phosphatase. The data indicate that Cdc28 and Ama1 function in a pathway to trigger Smk1-dependent steps in spore morphogenesis. We propose that this novel mechanism for controlling MAPK activation plays a role in coupling the completion of meiosis II to gamete formation.
Smk1是酿酒酵母中一种减数分裂特异性的丝裂原活化蛋白激酶(MAPK)同源物,可调节孢子形成的减数分裂后程序。与其他MAPK类似,它通过其调节环中T-X-Y基序的磷酸化而被激活,但控制Smk1激活的信号尚未明确。在这里,我们表明Ama1是后期促进复合物/细胞周期体(APC/C)的减数分裂特异性激活剂,在减数分裂过程中促进Smk1的激活。CDC28的一个弱化等位基因抑制了ama1缺失菌株的孢子形成缺陷,并增加了Smk1的激活状态。Ama1在调节Smk1中的功能独立于FEAR网络,FEAR网络通过Cdc14磷酸酶促进有丝分裂退出和减数分裂I退出。数据表明,Cdc28和Ama1在触发孢子形态发生中Smk1依赖性步骤的途径中发挥作用。我们提出,这种控制MAPK激活的新机制在将减数分裂II的完成与配子形成联系起来方面发挥作用。