Phosphorylation, disorder, and phase separation govern the behavior of Frequency in the fungal circadian clock
Year: 2023
Type: article
Abstract: Circadian clocks are composed of transcription-translation negative feedback loops that pace rhythms of gene expression to the diurnal cycle. In the filamentous fungus Neurospora crassa, the proteins F requency ( F RQ), the F RQ-interacting RNA helicase (FRH), and C asein-Kinase I (CK1) form the FFC complex that represses expression of genes activated by the white-collar complex (WCC). FRQ orchestrates key molecular interactions of the clock despite containing little predicted tertiary structure. Spin labeling and pulse-dipolar electron spin resonance spectroscopy provide domain-specific structural insights into the 989-residue intrinsically disordered FRQ and the FFC. FRQ contains a compact core that associates and organizes FRH and CK1 to coordinate their roles in WCC repression. FRQ phosphorylation increases conformational flexibility and alters oligomeric state, but the changes in structure and dynamics are non-uniform. Full-length FRQ undergoes liquid–liquid phase separation (LLPS) to sequester FRH and CK1 and influence CK1 enzymatic activity. Although FRQ phosphorylation favors LLPS, LLPS feeds back to reduce FRQ phosphorylation by CK1 at higher temperatures. Live imaging of Neurospora hyphae reveals FRQ foci characteristic of condensates near the nuclear periphery. Analogous clock repressor proteins in higher organisms share little position-specific sequence identity with FRQ; yet, they contain amino acid compositions that promote LLPS. Hence, condensate formation may be a conserved feature of eukaryotic clocks.
Source: eLife
DOI: 10.7554/elife.90259
Language: English
Subfield: Endocrine and Autonomic Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,500
Awards: G1430952875, G1762080133, G1974059531, G2579886042, Role of DNA Methylation in Liquid-liquid Phase Separation-mediated Heterochromatin Formation, G440393388, G522049510, OPERATION OF CORNELL HIGH ENERGY SYNCHROTRON SOURCE (CHESS), Elucidating the mechanism of MBD protein LLPS and its role in transcriptional repression, G6429492609, G6843289442, National Biomedical Center for Advanced ESR Technology (ACERT), G8676815010, Macromolecular Diffraction Resource: MacCHESS, National Biomedical Resource for Electron-Spin Resonance Spectroscopy (ACERT), Molecular mechanisms of signaling systems responsive to light, redox and chemical environment, MacCHESS Synchrotron Source for Structural Biology, Genetic and Molecular Dissection of the Neurospora Clock
OpenAlex ID: W4388971907
