Molecular-genetic Manipulation of the Suprachiasmatic Nucleus Circadian Clock. Issue 12 (29th May 2020)

• Record Type: Journal Article
• Authors: Hastings, Michael H.; Smyllie, Nicola J.; Patton, Andrew P.
• Is Part Of: Journal of molecular biology. Volume 432:Issue 12(2020)
• Page Start: 3639
• Page End: 3660
• Publication Date: 2020-05-29
• Subjects: neurons -- cryptochrome -- period -- translational switching -- astrocytes; Molecular biology -- Periodicals; Biology -- Periodicals; Biochemistry -- Periodicals; Bacteriology -- Periodicals; Molecular Biology -- Periodicals; Biochemistry -- Periodicals; Biologie moléculaire -- Périodiques; Biologie -- Périodiques; Biochimie -- Périodiques; Moleculaire biologie; Biochemistry; Biology; Molecular biology; Periodicals; 572.805
• DOI: 10.1016/j.jmb.2020.01.019
• Languages: English
• ISSNs: 0022-2836

Abstract

Abstract: Circadian (approximately daily) rhythms of physiology and behaviour adapt organisms to the alternating environments of day and night. The suprachiasmatic nucleus (SCN) of the hypothalamus is the principal circadian timekeeper of mammals. The mammalian cell-autonomous circadian clock is built around a self-sustaining transcriptional-translational negative feedback loop (TTFL) in which the negative regulators Per and Cry suppress their own expression, which is driven by the positive regulators Clock and Bmal1. Importantly, such TTFL-based clocks are present in all major tissues across the organism, and the SCN is their central co-ordinator. First, we analyse SCN timekeeping at the cell-autonomous and the circuit-based levels of organisation. We consider how molecular-genetic manipulations have been used to probe cell-autonomous timing in the SCN, identifying the integral components of the clock. Second, we consider new approaches that enable real-time monitoring of the activity of these clock components and clock-driven cellular outputs. Finally, we review how intersectional genetic manipulations of the cell-autonomous clockwork can be used to determine how SCN cells interact to generate an ensemble circadian signal. Critically, it is these network-level interactions that confer on the SCN its emergent properties of robustness, light-entrained phase and precision— properties that are essential for its role as the central co-ordinator. Remaining gaps in knowledge include an understanding of how the TTFL proteins behave individually and in complexes: whether particular SCN neuronal populations act as pacemakers, and if so, by which signalling mechanisms, and finally the nature of the recently discovered role of astrocytes within the SCN network. Graphical abstract: Image 1 Highlights: The suprachiasmatic nucleus (SCN) is the principal circadian clock of mammals. The SCN cell-autonomous clock is a transcription-translation negative feedback loop. Real-time imaging provides a window onto cellular and circuit-level timekeeping. Critical emergent properties of the SCN network arise by intercellular interactions. We do not know how clock proteins behave or how SCN cells interact to define time.