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CRYPTOCHROMES promote daily proteome homeostasis

ABSTRACT: The daily organisation of most mammalian cellular functions is attributed to circadian regulation of clock-controlled protein expression, driven by daily cycles of CRYPTOCHROME-dependent transcriptional feedback repression. To test this, we used quantitative mass spectrometry to compare wild type and CRY-deficient fibroblasts under constant conditions. In CRY-deficient cells, we found that temporal variation in protein, phosphopeptide, and K+ abundance was at least as great as wild type controls. Most strikingly. the extent of temporal variation within either genotype was much smaller than overall differences in proteome composition between WT and CRY-deficient cells. This proteome imbalance in CRY-deficient cells and tissues was associated with increased susceptibility to proteotoxic stress, which impairs circadian robustness, and may contribute to the wide-ranging phenotypes of CRY-deficient mice. Rather than generating largescale daily variation in proteome composition, we suggest it is plausible that the various transcriptional and post-translational functions of CRY proteins ultimately act to promote protein and osmotic homeostasis against daily perturbation.

INSTRUMENT(S): Q Exactive Plus

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Lung, Fibroblast

SUBMITTER: Sew Peak-Chew

LAB HEAD: John O'Neill

PROVIDER: PXD019499 | Pride | 2021-11-19

REPOSITORIES: Pride

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			Action	DRS
	CRM2962_WT1phos_F10.raw	Raw
	CRM2962_WT1phos_F11.raw	Raw
	CRM2962_WT1phos_F12.raw	Raw
	CRM2962_WT1phos_F13.raw	Raw
	CRM2962_WT1phos_F14.raw	Raw

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