SPATA18, a Spermatogenesis-Associated Gene, Is a Novel Transcriptional Target of p53 and p63

被引:34
作者
Bornstein, Chamutal [1 ]
Brosh, Ran [1 ]
Molchadsky, Alina [1 ]
Madar, Shalom [1 ]
Kogan-Sakin, Ira [1 ]
Goldstein, Ido [1 ]
Chakravarti, Deepavali [2 ]
Flores, Elsa R. [2 ]
Goldfinger, Naomi [1 ]
Sarig, Rachel [1 ]
Rotter, Varda [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[2] Univ Texas MD Anderson Canc Ctr, Grad Sch Biomed Sci, Dept Mol & Cellular Oncol, Houston, TX 77030 USA
关键词
P53-DEFICIENT MICE; MUTANT P53; SPONTANEOUS TUMORS; MIDDLE PIECE; RAT TESTIS; IN-VIVO; EXPRESSION; CANCER; FAMILY; DIFFERENTIATION;
D O I
10.1128/MCB.01072-10
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
The transcription factor p53 functions not only to suppress tumorigenesis but also to maintain normal development and homeostasis. Although p53 was implicated in different aspects of fertility, including spermatogenesis and implantation, the mechanism underlying p53 involvement in spermatogenesis is poorly resolved. In this study we describe the identification of a spermatogenesis-associated gene, SPATA18, as a novel p53 transcriptional target and show that SPATA18 transcription is induced by p53 in a variety of cell types of both human and mouse origin. p53 binds a consensus DNA motif that resides within the first intron of SPATA18. We describe the spatiotemporal expression patterns of SPATA18 in mouse seminiferous tubules and suggest that SPATA18 transcription is regulated in vivo by p53. We also demonstrate the induction of SPATA18 by p63 and suggest that p63 can compensate for the loss of p53 activity in vivo. Our data not only enrich the known collection of p53 targets but may also provide insights on spermatogenesis defects that are associated with p53 deficiency.
引用
收藏
页码:1679 / 1689
页数:11
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