Ikbkap/Elp1 Deficiency Causes Male Infertility by Disrupting Meiotic Progression

被引:42
|
作者
Lin, Fu-Jung [1 ,2 ,3 ]
Shen, Li [1 ,2 ,3 ]
Jang, Chuan-Wei [1 ]
Falnes, Pal O. [4 ]
Zhang, Yi [1 ,2 ,3 ,5 ]
机构
[1] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[4] Univ Oslo, Dept Biosci, Oslo, Norway
[5] Harvard Univ, Sch Med, Harvard Stem Cell Inst, Boston, MA 02115 USA
来源
PLOS GENETICS | 2013年 / 9卷 / 05期
关键词
SEX-CHROMOSOME INACTIVATION; TRANSFER-RNA; FAMILIAL DYSAUTONOMIA; MOUSE SPERMATOCYTES; ELONGATOR COMPLEX; MOLECULAR ARCHITECTURE; PSEUDOAUTOSOMAL REGION; MAMMALIAN MEIOSIS; MICE; TRANSCRIPTION;
D O I
10.1371/journal.pgen.1003516
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mouse Ikbkap gene encodes IKAP-one of the core subunits of Elongator-and is thought to be involved in transcription. However, the biological function of IKAP, particularly within the context of an animal model, remains poorly characterized. We used a loss-of-function approach in mice to demonstrate that Ikbkap is essential for meiosis during spermatogenesis. Absence of Ikbkap results in defects in synapsis and meiotic recombination, both of which result in increased apoptosis and complete arrest of gametogenesis. In Ikbkap-mutant testes, a few meiotic genes are down-regulated, suggesting IKAP's role in transcriptional regulation. In addition, Ikbkap-mutant testes exhibit defects in wobble uridine tRNA modification, supporting a conserved tRNA modification function from yeast to mammals. Thus, our study not only reveals a novel function of IKAP in meiosis, but also suggests that IKAP contributes to this process partly by exerting its effect on transcription and tRNA modification.
引用
收藏
页数:15
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