A PROP1-binding factor, AES cloned by yeast two-hybrid assay represses PROP1-induced Pit-1 gene expression

作者：Sugiyama Yuka; Ikeshita Nobuko; Shibahara Hiromi; Yamamoto Daisuke; Kawagishi Mayuko; Iguchi Genzo; Iida Keiji; Takahashi Yutaka; Kaji Hidesuke; Chihara Kazuo; Okimura Yasuhiko^*

来源：Molecular and Cellular Endocrinology, 2013, 376(1-2): 93-98.

DOI：10.1016/j.mce.2013.05.022

• AES
• PROP1
• TLE1
• Two-hybrid assay
• Pit-1
• CPHD

PROP1 mutation causes combined pituitary hormone deficiency (CPHD). Several mutations are located in a transactivation domain (TAD) of Prop1, and the loss of TAD binding to cofactors is likely the cause of CPHD. PROP1 cofactors have not yet been identified. In the present study, we aimed to identify the PROP1-interacting proteins from the human brain cDNA library. Using a yeast two-hybrid assay, we cloned nine candidate proteins that may bind to PROP1. Of those nine candidates, amino-terminal enhancer of split (AES) was the most abundant, and we analyzed the AES function. AES dose-dependently decreased the PROP1-induced Pit-1 reporter gene expression. An immunoprecipitation assay revealed the relationship between AES and PROP1. In a mammalian two-hybrid assay, a leucine zipper-like motif of the AES Q domain was identified as a region that interacted with TAD. These results indicated that AES was a corepressor of PROP1.

• 出版日期2013-8-25