Parp1-XRCC1 and the repair of DNA double strand breaks in mouse round spermatids

被引:53
作者
Ahmed, Emad A. [1 ]
de Boer, Peter [2 ]
Philippens, Marielle E. P. [3 ]
Kal, Henk B. [3 ]
de Rooij, Dirk G. [1 ,4 ]
机构
[1] Univ Utrecht, Fac Sci, Dept Endocrinol & Metab, NL-3584 CH Utrecht, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Obstet & Gynaecol, NL-6500 HB Nijmegen, Netherlands
[3] Univ Med Ctr Utrecht, Dept Radiotherapy, NL-3584 CX Utrecht, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Dept Reprod Med, NL-1105 AZ Amsterdam, Netherlands
关键词
Spermatogenesis; Non-homologous end joining; Homologous recombination; DNA repair; Ionizing radiation; BASE EXCISION-REPAIR; DEPENDENT PROTEIN-KINASE; POLY(ADP-RIBOSE) POLYMERASE; MEIOTIC PROPHASE; MAMMALIAN-CELLS; GAMMA-H2AX FOCI; GERM-CELLS; LIGASE-IV; X-RAY; DAMAGE;
D O I
10.1016/j.mrfmmm.2009.10.011
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The repair of DNA double strand breaks (DSBs) in male germ cells is slower and differently regulated compared to that in somatic cells. Round spermatids show DSB repair and are radioresistant to apoptosis induction. Mutation induction studies using ionizing irradiation, indicated a high frequency of chromosome aberrations (CA) in the next generation. Since they are in a G1 comparable stage of the cell cycle, haploid spermatids are expected to repair DSBs by the non-homologous end-joining pathway (NHEJ). However, immunohistochemical evidence indicates that not all components of the classical NHEJ pathway are available since the presence of DNA-PKcs cannot be shown. Here, we demonstrate that round spermatids, as well as most other types of male germ cells express both Parp1 and XRCC1. Therefore, we have determined whether the alternative Parp1/XRCC1 dependent NHEJ pathway is active in these nuclei and also have tested for classical NHEJ activity by a genetic method. To evaluate DSB repair in SCID mice, deficient for DNA-PKcs, and to study the involvement of the Parp1/XRCC1 dependent NHEJ pathway in round spermatids, the loss of gamma-H2AX foci after irradiation has been determined in nucleus spreads of round spermatids of SCID mice and in nucleus spreads and histological sections of Parp1-inhibited mice and their respective controls. Results show that around half of the breaks in randomly selected round spermatids are repaired between 1 and 8 h after irradiation. The repair of 16% of the induced DSBs requires DNA-PKcs and 21% Parp1. Foci numbers in the Parp1-inhibited testes tend to be higher in spermatids of all epithelial stages reaching significance in stages I-III which indicates an active Parp1/XRCC1 pathway in round spermatids and a decreased repair capacity in later round spermatid stages. In Parp1-inhibited SCID mice only 14.5% of the breaks were repaired 8 h after irradiation indicating additivity of the two NHEJ pathways in round spermatids. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 90
页数:7
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