Edwards Mathew D, Brancaccio Marco, Chesham Johanna E, Maywood Elizabeth S, Hastings Michael H
Division of Neurobiology, Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.
Division of Neurobiology, Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom
Proc Natl Acad Sci U S A. 2016 Mar 8;113(10):2732-7. doi: 10.1073/pnas.1519044113. Epub 2016 Feb 22.
Circadian rhythms in mammals are coordinated by the suprachiasmatic nucleus (SCN). SCN neurons define circadian time using transcriptional/posttranslational feedback loops (TTFL) in which expression of Cryptochrome (Cry) and Period (Per) genes is inhibited by their protein products. Loss of Cry1 and Cry2 stops the SCN clock, whereas individual deletions accelerate and decelerate it, respectively. At the circuit level, neuronal interactions synchronize cellular TTFLs, creating a spatiotemporal wave of gene expression across the SCN that is lost in Cry1/2-deficient SCN. To interrogate the properties of CRY proteins required for circadian function, we expressed CRY in SCN of Cry-deficient mice using adeno-associated virus (AAV). Expression of CRY1::EGFP or CRY2::EGFP under a minimal Cry1 promoter was circadian and rapidly induced PER2-dependent bioluminescence rhythms in previously arrhythmic Cry1/2-deficient SCN, with periods appropriate to each isoform. CRY1::EGFP appropriately lengthened the behavioral period in Cry1-deficient mice. Thus, determination of specific circadian periods reflects properties of the respective proteins, independently of their phase of expression. Phase of CRY1::EGFP expression was critical, however, because constitutive or phase-delayed promoters failed to sustain coherent rhythms. At the circuit level, CRY1::EGFP induced the spatiotemporal wave of PER2 expression in Cry1/2-deficient SCN. This was dependent on the neuropeptide arginine vasopressin (AVP) because it was prevented by pharmacological blockade of AVP receptors. Thus, our genetic complementation assay reveals acute, protein-specific induction of cell-autonomous and network-level circadian rhythmicity in SCN never previously exposed to CRY. Specifically, Cry expression must be circadian and appropriately phased to support rhythms, and AVP receptor signaling is required to impose circuit-level circadian function.
哺乳动物的昼夜节律由视交叉上核(SCN)协调。SCN神经元利用转录/翻译后反馈回路(TTFL)来确定昼夜时间,在该回路中,隐花色素(Cry)和周期(Per)基因的表达受到其蛋白质产物的抑制。Cry1和Cry2的缺失会使SCN时钟停止,而单个基因的缺失则分别使其加速和减速。在回路水平上,神经元相互作用使细胞TTFL同步,在整个SCN中产生基因表达的时空波,而在Cry1/2缺陷的SCN中这种波消失。为了探究昼夜节律功能所需的CRY蛋白的特性,我们使用腺相关病毒(AAV)在Cry缺陷小鼠的SCN中表达CRY。在最小Cry1启动子下CRY1::EGFP或CRY2::EGFP的表达具有昼夜节律性,并在先前无节律的Cry1/2缺陷SCN中迅速诱导依赖PER2的生物发光节律,其周期与每种异构体相适应。CRY1::EGFP适当延长了Cry1缺陷小鼠的行为周期。因此,特定昼夜周期的确定反映了各自蛋白质的特性,与其表达阶段无关。然而,CRY1::EGFP表达的阶段至关重要,因为组成型或相位延迟的启动子无法维持连贯的节律。在回路水平上,CRY1::EGFP在Cry1/2缺陷的SCN中诱导了PER2表达的时空波。这依赖于神经肽精氨酸加压素(AVP),因为AVP受体的药理学阻断可阻止这种现象。因此,我们的基因互补试验揭示了在从未接触过CRY的SCN中,细胞自主和网络水平的昼夜节律性的急性、蛋白质特异性诱导。具体而言,Cry表达必须具有昼夜节律性且相位适当以支持节律,并且需要AVP受体信号传导来赋予回路水平的昼夜节律功能。