Induction of the SHARP-2 mRNA level by insulin is mediated by multiple signaling pathways

Author:

Kanai Yukiko1,Asano Kosuke2,Komatsu Yoshiko1,Takagi Katsuhiro12,Ono Moe3,Tanaka Takashi3,Tomita Koji3,Haneishi Ayumi2,Tsukada Akiko2,Yamada Kazuya12

Affiliation:

1. Graduate School of Health Science, Matsumoto University, Matsumoto, Japan

2. Faculty of Human Health Science, Department of Health and Nutritional Science, Matsumoto University, Matsumoto, Japan

3. Faculty of Pharmacy, Laboratory of Molecular Biology, Osaka Ohtani University, Tondabayashi, Japan

Abstract

Abstract The rat enhancer of split- and hairy-related protein-2 (SHARP-2) is an insulin-inducible transcription factor which represses transcription of the rat phosphoenolpyruvate carboxykinase gene. In this study, a regulatory mechanism of the SHARP-2 mRNA level by insulin was analyzed. Insulin rapidly induced the level of SHARP-2 mRNA. This induction was blocked by inhibitors for phosphoinositide 3-kinase (PI 3-K), protein kinase C (PKC), and mammalian target of rapamycin (mTOR), actinomycin D, and cycloheximide. Whereas an adenovirus infection expressing a dominant negative form of atypical PKC lambda (aPKCλ) blocked the insulin-induction of the SHARP-2 mRNA level, insulin rapidly activated the mTOR. Insulin did not enhance transcriptional activity from a 3.7 kb upstream region of the rat SHARP-2 gene. Thus, we conclude that insulin induces the expression of the rat SHARP-2 gene at the transcription level via both a PI 3-K/aPKCλ- and a PI 3-K/mTOR- pathways and that protein synthesis is required for this induction.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Research Activity of Matsumoto University

Publisher

Oxford University Press (OUP)

Subject

Organic Chemistry,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Biochemistry,Analytical Chemistry,Biotechnology

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