Rex1 (Zfp42) null mice show impaired testicular function, abnormal testis morphology, and aberrant gene expression.

TitleRex1 (Zfp42) null mice show impaired testicular function, abnormal testis morphology, and aberrant gene expression.
Publication TypeJournal Article
Year of Publication2011
AuthorsRezende NC, Lee M-Y, Monette S, Mark W, Lu A, Gudas LJ
JournalDev Biol
Volume356
Issue2
Pagination370-82
Date Published2011 Aug 15
ISSN1095-564X
KeywordsAnimals, Apoptosis, Cell Cycle, Female, Gene Expression Profiling, Male, Mice, Mice, Inbred C57BL, Ovary, p38 Mitogen-Activated Protein Kinases, Seminiferous Tubules, Sperm Count, STAT3 Transcription Factor, Testis, Transcription Factors
Abstract

Rex1 (Zfp42), GeneID 132625, is a gene whose expression is closely associated with pluripotency/multipotency in both mouse and human embryonic stem cells. To study the function of the murine Rex1 gene in vivo, we have used cre/lox technology to create Rex1(floxed) mice and mice deficient in Rex1 gene function. Rex1(-/-)males are characterized by an age-associated decrease in sperm counts, abnormal sperm morphology, and mild testicular atrophy. We characterized global patterns of gene expression in primary germ cells by microarray and identified the growth hormone responsive gene, GRTP1, as a transcript present at a 4.5 fold higher level in wild type (WT) compared to Rex1(-/-) mice. We analyzed immature germ cell (Dazl), proliferating (PCNA), and Sertoli cell populations, and quantitated levels of apoptosis in Rex1(-/-) as compared to WT testes. We evaluated the expression of proteins previously reported to correlate with Rex1 expression, such as STAT3, phospho-STAT3, p38, and phospho-p38 in the testis. We report a distinct cellular localization of total STAT3 protein in Rex1(-/-) affected testes. Our data suggest that loss of Rex1 leads to impaired testicular function.

DOI10.1016/j.ydbio.2011.05.664
Alternate JournalDev. Biol.
PubMed ID21641340
PubMed Central IDPMC3214085
Grant ListR01 CA043796-20A1 / CA / NCI NIH HHS / United States
R01CA043796 / CA / NCI NIH HHS / United States
R01 CA043796-21 / CA / NCI NIH HHS / United States
/ / Howard Hughes Medical Institute / United States
R01 CA043796-22 / CA / NCI NIH HHS / United States
R01 CA043796 / CA / NCI NIH HHS / United States
R01 DE010389 / DE / NIDCR NIH HHS / United States