Format

Send to

Choose Destination
Genetics. 2016 Sep;204(1):163-76. doi: 10.1534/genetics.116.191064. Epub 2016 Jul 22.

Modulation of Circadian Gene Expression and Metabolic Compensation by the RCO-1 Corepressor of Neurospora crassa.

Author information

1
Millennium Nucleus for Fungal Integrative and Synthetic Biology, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago RM 114-D, Chile.
2
Department of Genetics, Geisel School of Medicine at Dartmouth College, Hanover, New Hampshire 03755.
3
Department of Biochemistry, Geisel School of Medicine at Dartmouth College, Hanover, New Hampshire 03755.
4
Department of Genetics, Geisel School of Medicine at Dartmouth College, Hanover, New Hampshire 03755 Department of Biochemistry, Geisel School of Medicine at Dartmouth College, Hanover, New Hampshire 03755.
5
Millennium Nucleus for Fungal Integrative and Synthetic Biology, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago RM 114-D, Chile llarrondo@bio.puc.cl.

Abstract

Neurospora crassa is a model organism for the study of circadian clocks, molecular machineries that confer ∼24-hr rhythms to different processes at the cellular and organismal levels. The FREQUENCY (FRQ) protein is a central component of the Neurospora core clock, a transcription/translation negative feedback loop that controls genome-wide rhythmic gene expression. A genetic screen aimed at determining new components involved in the latter process identified regulation of conidiation 1 (rco-1), the ortholog of the Saccharomyces cerevisiae Tup1 corepressor, as affecting period length. By employing bioluminescent transcriptional and translational fusion reporters, we evaluated frq and FRQ expression levels in the rco-1 mutant background observing that, in contrast to prior reports, frq and FRQ expression are robustly rhythmic in the absence of RCO-1, although both amplitude and period length of the core clock are affected. Moreover, we detected a defect in metabolic compensation, such that high-glucose concentrations in the medium result in a significant decrease in period when RCO-1 is absent. Proteins physically interacting with RCO-1 were identified through co-immunoprecipitation and mass spectrometry; these include several components involved in chromatin remodeling and transcription, some of which, when absent, lead to a slight change in period. In the aggregate, these results indicate a dual role for RCO-1: although it is not essential for core-clock function, it regulates proper period and amplitude of core-clock dynamics and is also required for the rhythmic regulation of several clock-controlled genes.

KEYWORDS:

Neurospora crassa; circadian clocks; core-clock mechanism; corepressor; frequency

PMID:
27449058
PMCID:
PMC5012383
DOI:
10.1534/genetics.116.191064
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for HighWire Icon for PubMed Central
Loading ...
Support Center