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雄性小鼠减数分裂的生化分析。II. 粗线期的DNA代谢

Biochemical analysis of meiosis in the male mouse. II. DNA metabolism at pachytene.

作者信息

Hotta Y, Chandley A C, Stern H

出版信息

Chromosoma. 1977 Jul 8;62(3):255-68. doi: 10.1007/BF00286047.

Abstract

The DNA metabolism of mouse spermatogenic cells was investigated by intravenous administration of isotope and Staput fractionation of the cells. The pattern of metabolism is virtually identical with that observed in Lilium microsporocytes. A programmed single strand nicking of DNA occure at pachytene such that at least 50% of the DNA is in the form of 62S fragments. Repair replication of endogenously nicked sites is fully achieved during pachytene. The sites of nicking and repair are preferentially located in sequences that are repeated about 400 times. These results are considered as strong evidence for a universal pattern of meiotic prophase DNA metabolism which is associated with crossing-over.

摘要

通过静脉注射同位素和细胞的斯塔普特分级分离法研究了小鼠生精细胞的DNA代谢。其代谢模式与在百合小孢子母细胞中观察到的模式几乎相同。在粗线期发生程序性的DNA单链切口,使得至少50%的DNA呈62S片段的形式。内源性切口位点的修复复制在粗线期完全完成。切口和修复位点优先位于重复约400次的序列中。这些结果被视为减数分裂前期DNA代谢与交叉相关的普遍模式的有力证据。

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