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PMID: 18579725 Published · ppublish English

Identification of NR5A1 (SF-1/AD4BP) gene expression modulators by large-scale gain and loss of function studies.

The Journal of endocrinology ·Vol. 198 ·No. 3 ·2009-07-10

Sakai Noriko, Terami Hiromi, Suzuki Shinobu, Haga Megumi, Nomoto Ken, Tsuchida Nobuko, Morohashi Ken-ichirou, Saito Naoaki, Asada Maki, Hashimoto Megumi, Harada Daisuke, Asahara Hiroshi, Ishikawa Tetsuya, Shimada Fumiki, Sakurada Kazuhiro

Abstract

Nuclear receptor subfamily 5, group A, member 1 (NR5A1 previously known as SF-1/AD4BP) is a transcription factor involved in the development of adrenal/gonadal tissues and steroidogenic lineage cell differentiation in adult somatic stem cells. To understand the cellular signaling network that regulates NR5A1 gene expression, loss of function screening with an siRNA kinome library, and gain of function screening with an addressable full-length cDNA library representing one quarter of the human genome was carried out. The NR5A1 gene expression was activated in mesenchymal stem cells by siRNA directed against protein kinase C (PKC)-delta, erb-B3, RhoGAP (ARHGAP26), and hexokinase 2, none of which were previously known to be involved in the NR5A1 gene expression. Among these, we identified crosstalk between erb-B3 and PKC-delta signaling cascades. In addition, the gain of function studies indicated that sex-determining region Y (SRY)-box 15 (SOX15), TEA domain family member 4, KIAA1257 (a gene of unknown function), ADAM metallopeptidase with thrombospondin type 1 motif 6, Josephin domain containing 1, centromere protein, TATA box-binding protein-associated factor 5-like RNA polymerase, and inducible T-cell co-stimulator activate NR5A1 gene expression. These results provide new insights into the molecular mechanisms of NR5A1 gene expression.

Article Info
Journal
The Journal of endocrinology
Abbr.
J Endocrinol
Published
2009-07-10
Indexed
2008-08-27
Updated
2014-11-20
Language
English
Country/Region
England
NLM ID
0375363
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