Cell and tissue‐autonomous development of the circadian clock in mouse embryos. Issue 3 (25th December 2013)

• Record Type: Journal Article
• Authors: Inada, Yutaka; Uchida, Hitoshi; Umemura, Yasuhiro; Nakamura, Wataru; Sakai, Takayoshi; Koike, Nobuya; Yagita, Kazuhiro
• Is Part Of: FEBS letters. Volume 588:Issue 3(2014)
• Page Start: 459
• Page End: 465
• Publication Date: 2013-12-25
• Subjects: Circadian rhythm -- Development -- Embryo -- Cellular differentiation; Biochemistry -- Periodicals; Biophysics -- Periodicals; Molecular biology -- Periodicals; Biochimie -- Périodiques; Biochemistry; Biophysics; Molecular biology; Periodicals; 572.05
• DOI: 10.1016/j.febslet.2013.12.007
• Languages: English
• ISSNs: 0014-5793

Abstract

Abstract : The emergence of the circadian rhythm is a dramatic and physiologically essential event for mammals to adapt to daily environmental cycles. It has been demonstrated that circadian rhythms develop during the embryonic stage even when the maternal central pacemaker suprachiasmatic nucleus has been disrupted. However, the mechanisms controlling development of the circadian clock are not yet fully understood. Here, we show that the circadian molecular oscillation in primary dispersed embryonic cells and explanted salivary glands obtained from mPER2 Luc mice embryos developed cell‐ or tissue‐autonomously even in tissue culture conditions. Moreover, the circadian clock in the primary mPER2 Lu c fibroblasts could be reprogrammed by the expression of the reprogramming factors. These findings suggest that mammalian circadian clock development may interact with cellular differentiation mechanisms. Abstract : Cell‐autonomous development of the circadian clock in mouse embryonic peripheral cells in vitro . Tissue‐autonomous development of the circadian clock in mouse salivary gland organ ex vivo . Recapitulation of mPER2::Luc driven circadian oscillation after redifferentiation of mPER2 Luc MEF‐derived iPS cells.