Transactivation mechanisms of mouse clock transcription factors, mClock and mArnt3

Sho Takahata, Takahiro Ozaki, Junsei Mimura, Yasuo Kikuchi, Kazuhiro Sogawa, Yoshiaki Fujii-Kuriyama

    Research output: Contribution to journalArticlepeer-review

    78 Citations (Scopus)

    Abstract

    Background: The Arnt3 (also termed as BMAL1 or MOP3)/Clock heterodimer is a positive regulator of circadian rhythm and activates the transcription of target genes such as per1 and vasopressin. Results: We investigated the transcriptional mechanism of mArnt3/mClock heterodimer. While mClock did not possess any distinct activation domain, mArnt3 contained a transcriptional activation domain at the most C-terminal end, the activity of which was not expressed, even in the one hybrid system, until it was bound by mClock. It has been suggested that mClock plays a regulatory or structural role in exerting a transcription enhancing effect of the mArnt3/mClock heterodimer. Deletion proceeding from amino acids 559-492 of mClock markedly reduced the transactivation activity of mArnt3/mClock heterodimer, in consistence with the results of the Clock-Δ19 mutant. Yeast and mammalian two-hybrid systems revealed that CBP and p300 interacted with mArnt3 via the CREB binding domain. The In vivo interaction between mArnt3 and CBP was confirmed by the GST pull down assay. Conclusion: Taken together, these results suggest that the mArnt3/mClock heterodimer exerted its transactivation activity via CBP or p300 interacting with mArnt3 in the heterodimer with mClock playing a structural or regulatory role in the transactivation process.

    Original languageEnglish
    Pages (from-to)739-747
    Number of pages9
    JournalGenes to Cells
    Volume5
    Issue number9
    DOIs
    Publication statusPublished - 2000

    ASJC Scopus subject areas

    • Genetics
    • Cell Biology

    Fingerprint Dive into the research topics of 'Transactivation mechanisms of mouse clock transcription factors, mClock and mArnt3'. Together they form a unique fingerprint.

    Cite this