Regulation of meiosis during mammalian spermatogenesis: The A-type cyclins and their associated cyclin-dependent kinases are differentially expressed in the germ-cell lineage

被引:105
作者
Ravnik, SE [1 ]
Wolgemuth, DJ
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Dept Biochem & Cell Biol, Lubbock, TX 79430 USA
[2] Columbia Univ Coll Phys & Surg, Dept Genet & Dev, New York, NY 10032 USA
[3] Columbia Univ Coll Phys & Surg, Dept Obstet & Gynecol, New York, NY 10032 USA
[4] Columbia Univ Coll Phys & Surg, Ctr Reprod Sci, New York, NY 10032 USA
[5] Columbia Univ Coll Phys & Surg, Inst Human Nutr, New York, NY 10032 USA
[6] Columbia Univ Coll Phys & Surg, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
关键词
cell cycle; germ line; mouse gametogenesis; meiosis;
D O I
10.1006/dbio.1998.9156
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
To begin to examine the function of the A-type cyclins during meiosis in the male, we have examined the developmental and cellular distribution of the cyclin A1 and cyclin A2 proteins, as well as their candidate cyclin-dependent kinase partners, Cdk1 and Cdk2, in the spermatogenic lineage. Immunohistochemical localization revealed that cyclin Al is present only in male germ cells just prior to or during the first, but not the second, meiotic division. By contrast, cyclin A2 was expressed in spermatogonia and was most abundant in preleptotene spermatocytes, cells which will enter the meiotic pathway. Immunohistochemical detection of Cdk1 was most apparent in early pachytene spermatocytes, while staining intensity diminished in diplotene and meiotically dividing spermatocytes, the cells in which cyclin A1 expression was strongest. Cdk2 was highly expressed in all spermatocytes. Notably, in cells undergoing the meiotic reduction divisions, Cdk2 appeared to localize specifically to the chromatin. This was not the case for spermatogonia undergoing mitotic divisions. In the testis, cyclin Al has been shown to bind both Cdk1 and Cdk2 but we show here that cyclin A2 binds only Cdk2. These results indicate that the A-type cyclins and their associated kinases have different functions in the initiation and passage of male germ cells through meiosis. (C) 1999 Academic Press.
引用
收藏
页码:408 / 418
页数:11
相关论文
共 49 条
[1]   CYCLIN-A AND THE RETINOBLASTOMA GENE-PRODUCT COMPLEX WITH A COMMON TRANSCRIPTION FACTOR [J].
BANDARA, LR ;
ADAMCZEWSKI, JP ;
HUNT, T ;
LATHANGUE, NB .
NATURE, 1991, 352 (6332) :249-251
[2]   SPERMATOGENIC CELLS OF PREPUBERAL MOUSE - ISOLATION AND MORPHOLOGICAL CHARACTERIZATION [J].
BELLVE, AR ;
CAVICCHIA, JC ;
MILLETTE, CF ;
OBRIEN, DA ;
BHATNAGAR, YM ;
DYM, M .
JOURNAL OF CELL BIOLOGY, 1977, 74 (01) :68-85
[3]   NERVE GROWTH-FACTOR REGULATES THE EXPRESSION AND ACTIVITY OF P33(CDK2) AND P34(CDC2) KINASES IN PC12 PHEOCHROMOCYTOMA CELLS [J].
BUCHKOVICH, KJ ;
ZIFF, EB .
MOLECULAR BIOLOGY OF THE CELL, 1994, 5 (11) :1225-1241
[4]   REVERSAL OF TERMINAL DIFFERENTIATION AND CONTROL OF DNA-REPLICATION - CYCLIN-A AND CDK2 SPECIFICALLY LOCALIZE AT SUBNUCLEAR SITES OF DNA-REPLICATION [J].
CARDOSO, MC ;
LEONHARDT, H ;
NADALGINARD, B .
CELL, 1993, 74 (06) :979-992
[5]  
CHAPMAN DL, 1993, DEVELOPMENT, V118, P229
[6]   THE CYCLIN-DEPENDENT PROTEIN-KINASES AND THE CONTROL OF CELL-DIVISION .1. [J].
DOREE, M ;
GALAS, S .
FASEB JOURNAL, 1994, 8 (14) :1114-1121
[7]   CDK2 ENCODES A 33-KDA CYCLIN-A-ASSOCIATED PROTEIN-KINASE AND IS EXPRESSED BEFORE CDC2 IN THE CELL-CYCLE [J].
ELLEDGE, SJ ;
RICHMAN, R ;
HALL, FL ;
WILLIAMS, RT ;
LODGSON, N ;
HARPER, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :2907-2911
[8]   CYCLIN - A PROTEIN SPECIFIED BY MATERNAL MESSENGER-RNA IN SEA-URCHIN EGGS THAT IS DESTROYED AT EACH CLEAVAGE DIVISION [J].
EVANS, T ;
ROSENTHAL, ET ;
YOUNGBLOM, J ;
DISTEL, D ;
HUNT, T .
CELL, 1983, 33 (02) :389-396
[9]   A NOVEL CYCLIN ASSOCIATES WITH MO15/CDK7 TO FORM THE CDK-ACTIVATING KINASE [J].
FISHER, RP ;
MORGAN, DO .
CELL, 1994, 78 (04) :713-724
[10]   REQUIREMENT FOR CDK2 IN CYTOSTATIC FACTOR MEDIATED METAPHASE-II ARREST [J].
GABRIELLI, BG ;
ROY, LM ;
MALLER, JL .
SCIENCE, 1993, 259 (5102) :1766-1769