Literature DB >> 12852854

jumonji downregulates cardiac cell proliferation by repressing cyclin D1 expression.

Masashi Toyoda1, Haruki Shirato, Kuniko Nakajima, Mizuyo Kojima, Miho Takahashi, Misae Kubota, Rika Suzuki-Migishima, Yoshiko Motegi, Minesuke Yokoyama, Takashi Takeuchi.   

Abstract

Spatiotemporal regulation of cell proliferation is necessary for normal tissue development. The molecular mechanisms, especially the signaling pathways controlling the cell cycle machinery, remain largely unknown. Here, we demonstrate a negative relationship between the spatiotemporal patterns of jumonji (jmj) expression and cardiac myocyte proliferation. cyclin D1 expression and cell proliferation are enhanced in the cardiac myocytes of jmj-deficient mutant embryos. In contrast, jmj overexpression represses cyclin D1 expression in cardiac cells, and Jmj protein binds to cyclin D1 promoter in vivo and represses its transcriptional activity. cyclin D1 overexpression causes hyperproliferation in the cardiac myocytes, but the absence of cyclin D1 in jmj mutant embryos rescues the hyperproliferation. Therefore, Jmj might control cardiac myocyte proliferation and consequently cardiac morphogenesis by repressing cyclin D1 expression.

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Year:  2003        PMID: 12852854     DOI: 10.1016/s1534-5807(03)00189-8

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  54 in total

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