Human FATE is a novel X-linked gene expressed in fetal and adult testis

Citation
C. Olesen et al., Human FATE is a novel X-linked gene expressed in fetal and adult testis, MOL C ENDOC, 184(1-2), 2001, pp. 25-32
Citations number
30
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
MOLECULAR AND CELLULAR ENDOCRINOLOGY
ISSN journal
03037207 → ACNP
Volume
184
Issue
1-2
Year of publication
2001
Pages
25 - 32
Database
ISI
SICI code
0303-7207(20011126)184:1-2<25:HFIANX>2.0.ZU;2-6
Abstract
Previously, we identified a partial cDNA sequence of a novel human transcri pt, designated fetal and adult testis expressed transcript (FATE). FATE is testis-specific in fetal life and co-expressed with SRY in a 7 weeks old fe tal testis, suggesting a function in early testicular differentiation. Here in, full-length cDNA clones of human and porcine FATE were isolated and the gene structure and promoter region of the human FATE gene was characterize d. The human FATE gene, which maps to Xq28, consists of five exons spanning approximately 7 kb of genomic DNA. Examination of I kb of the FATE promote r region revealed the presence of a putative steroidogenic factor I (SF-1) binding site at position - 79 to - 71 upstream of the transcription start s ite. We propose that FATE might represent a novel target gene of SF-1 in hu man testicular differentiation and/or germ cell development. (C) 2001 Publi shed by Elsevier Science Ireland Ltd.