Mitogen-activated protein kinase phosphorylates and negatively regulates basic helix-loop-helix-PAS transcription factor BMAL1

Kamon Sanada, Toshiyuki Okano, Yoshitaka Fukada

Research output: Contribution to journalArticle

106 Citations (Scopus)

Abstract

In vertebrates, mitogen-activated protein kinase (MAPK) exhibits circadian activation in several clock structures and likely participates in the timekeeping mechanism of the circadian clock. Here we show that MAPK associates with a basic helix-loop-helix-PAS transcription factor BMAL1, a positive regulator for the autoregulatory feedback loop of the circadian oscillator. MAPK phosphorylates BMAL1 at multiple sites, including Ser-527, Thr-534, and Ser-599, in vitro, and BMAL1: CLOCK-induced transactivation from the E-box element is inhibited by expression of a constitutive active form of MAPK kinase in 293 cells. The inhibitory effect is reversed by coexpression of the kinase-dead mutant of MAPK or by mutation of BMAL1 at Thr-534. These results indicate that BMAL1:CLOCK-induced transcription is negatively regulated by MAPK-mediated phosphorylation of BMAL1 at Thr-534 and suggest a molecular link between circadian-activated MAPK and the clock oscillator.

Original languageEnglish
Pages (from-to)267-271
Number of pages5
JournalJournal of Biological Chemistry
Volume277
Issue number1
DOIs
Publication statusPublished - 2002 Jan 4
Externally publishedYes

Fingerprint

Basic Helix-Loop-Helix Transcription Factors
Mitogen-Activated Protein Kinases
Transcription Factors
Clocks
E-Box Elements
Circadian Clocks
Phosphorylation
Mitogen-Activated Protein Kinase Kinases
Transcription
Transcriptional Activation
Vertebrates
Phosphotransferases
Chemical activation
Feedback
Mutation

ASJC Scopus subject areas

  • Biochemistry

Cite this

Mitogen-activated protein kinase phosphorylates and negatively regulates basic helix-loop-helix-PAS transcription factor BMAL1. / Sanada, Kamon; Okano, Toshiyuki; Fukada, Yoshitaka.

In: Journal of Biological Chemistry, Vol. 277, No. 1, 04.01.2002, p. 267-271.

Research output: Contribution to journalArticle

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