Chapman D L, Wolgemuth D J
Department of Genetics and Development, Columbia University College of Physicians and Surgeons, New York, New York 10032.
Dev Biol. 1994 Oct;165(2):500-6. doi: 10.1006/dbio.1994.1270.
While the role of M-phase promoting factor (MPF) in controlling meiosis in oocytes has been well documented, very little is known about its function in male germ cells. Previous studies have localized transcripts for cyclin B1, the regulatory subunit of MPF, in male germ cells, with highest levels in postmeiotic, early round spermatids and much reduced levels in the meiotically dividing pachytene spermatocytes. The present study describes the localization of the regulatory and the catalytic subunits of MPF, CycB1 and Cdc2, respectively, to specific cell types within the testis. Immunoblotting revealed that both CycB1 and Cdc2 were present at highest levels in pachytene spermatocytes, with lower levels observed in the postmeiotic compartment. To assay for MPF activity, kinase complexes were isolated from lysates of testicular cells using p13suc1 agarose and antibodies directed against Cdc2 and CycB1. Activity of these kinase complexes was analyzed using histone H1 as an exogenous substrate. Cdc2 and CycB1-associated kinase activities were localized to the meiotically dividing pachytene spermatocytes, but not to postmeiotic spermatids.
虽然有充分的文献记载M期促进因子(MPF)在控制卵母细胞减数分裂中的作用,但对其在雄性生殖细胞中的功能却知之甚少。先前的研究已将MPF的调节亚基细胞周期蛋白B1的转录本定位在雄性生殖细胞中,在减数分裂后的早期圆形精子细胞中水平最高,而在进行减数分裂的粗线期精母细胞中水平则大大降低。本研究描述了MPF的调节亚基和催化亚基,即细胞周期蛋白B1(CycB1)和细胞周期蛋白依赖性激酶2(Cdc2),在睾丸内特定细胞类型中的定位。免疫印迹显示,CycB1和Cdc2在粗线期精母细胞中的水平最高,而在减数分裂后部分中的水平较低。为了检测MPF活性,使用p13suc1琼脂糖和针对Cdc2和CycB1的抗体从睾丸细胞裂解物中分离激酶复合物。使用组蛋白H1作为外源底物分析这些激酶复合物的活性。与Cdc2和CycB1相关的激酶活性定位于进行减数分裂的粗线期精母细胞,而不是减数分裂后的精子细胞。