Role of HP1β during spermatogenesis and DNA replication

被引：7

作者：

Charaka, Vijay ^{[1
]}

Tiwari, Anjana ^{[1
]}

Pandita, Raj K. ^{[1
,2
]}

Hunt, Clayton R. ^{[1
]}

Pandita, Tej K. ^{[1
,2
]}

机构：

[1] Houston Methodist Res Inst, Dept Radiat Oncol, Houston, TX 77030 USA

[2] Baylor Coll Med, Mol & Cellular Biol, Houston, TX 77030 USA

来源：

CHROMOSOMA | 2020年 / 129卷 / 3-4期

关键词：

HP1; beta; Spermatogenesis; DNA replication; Fork stability; Homologous recombination; HETEROCHROMATIN PROTEIN-1; MEIOTIC RECOMBINATION; TUMOR SUPPRESSION; CROSSING-OVER; PROPHASE I; DAMAGE; HP1; REPAIR; DROSOPHILA; ISOFORMS;

D O I：

10.1007/s00412-020-00739-4

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Heterochromatin protein 1 beta (HP1 beta), encoded by the Cbx1 gene, has been functionally linked to chromatin condensation, transcriptional regulation, and DNA damage repair. Here we report that testis-specific Cbx1 conditional knockout (Cbx1 cKO) impairs male germ cell development in mice. Depletion of HP1 beta negatively affected sperm maturation and increased seminiferous tubule degeneration in Cbx1 cKO mice. In addition, the spermatogonia have elevated gamma-H2AX foci levels as do Cbx1 deficient mouse embryonic fibroblasts (MEFs) as compared to wild-type (WT) control MEFs. The increase in gamma-H2AX foci in proliferating Cbx1 cKO cells indicates defective replication-dependent DNA damage repair. Depletion or loss of HP1 beta from human cells and MEFs increased DNA replication fork stalling and firing of new origins of replication, indicating defective DNA synthesis. Taken together, these results suggest that loss of HP1 beta in proliferating cells leads to DNA replication defects with associated DNA damage that impact spermatogenesis.

引用

页码：215 / 226

页数：12

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