Cyclin A1 is required for meiosis in the male mouse

被引:0
作者
Dong Liu
Martin M. Matzuk
Weng Kong Sung
Qiuxia Guo
Pei Wang
Debra J. Wolgemuth.
机构
[1] Integrated Program in Cellular,Department of Pathology
[2] Molecular and Biophysical Studies,Department of Cell Biology
[3] Columbia University College of Physicians and Surgeons,Department of Molecular and Human Genetics
[4] Baylor College of Medicine,Department of Genetics and Development
[5] Baylor College of Medicine,undefined
[6] Baylor College of Medicine,undefined
[7] Center for Reproductive Sciences,undefined
[8] Columbia University College of Physicians and Surgeons,undefined
[9] Columbia University College of Physicians and Surgeons,undefined
[10] Institute of Human Nutrition,undefined
[11] Columbia University College of Physicians and Surgeons,undefined
[12] Irving Comprehensive Cancer Center,undefined
[13] Columbia University College of Physicians and Surgeons,undefined
来源
Nature Genetics | 1998年 / 20卷
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摘要
The mammalian A-type cyclin family consists of two members, cyclin A1 (encoded by Ccna1) and cyclin A2 (encoded by Ccna2). Cyclin A2 promotes both G1/S and G2/M transitions1,2, and targeted deletion of Ccna2 in mouse is embryonic lethal3. Cyclin A1 is expressed in mice exclusively in the germ cell lineage4 and is expressed in humans at highest levels in the testis and certain myeloid leukaemia cells5,6. To investigate the role of cyclin A1 and possible redundancy among the cyclins in vivo, we generated mice bearing a null mutation of Ccna1. Ccna1-/- males were sterile due to a block of spermatogenesis before the first meiotic division, whereas females were normal. Meiosis arrest in Ccna1–/– males was associated with increased germ cell apoptosis, desynapsis abnormalities and reduction of Cdc2 kinase activation at the end of meiotic prophase. Cyclin A1 is therefore essential for spermatocyte passage into the first meiotic division in male mice, a function that cannot be complemented by the concurrently expressed B-type cyclins.
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页码:377 / 380
页数:3
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