Literature DB >> 9115195

Neurospora wc-1 and wc-2: transcription, photoresponses, and the origins of circadian rhythmicity.

S K Crosthwaite1, J C Dunlap, J J Loros.   

Abstract

Circadian rhythmicity is universally associated with the ability to perceive light, and the oscillators ("clocks") giving rise to these rhythms, which are feedback loops based on transcription and translation, are reset by light. Although such loops must contain elements of positive and negative regulation, the clock genes analyzed to date-frq in Neurospora and per and tim in Drosophila-are associated only with negative feedback and their biochemical functions are largely inferred. The white collar-1 and white collar-2 genes, both global regulators of photoresponses in Neurospora, encode DNA binding proteins that contain PAS domains and are believed to act as transcriptional activators. Data shown here suggest that wc-1 is a clock-associated gene and wc-2 is a clock component; both play essential roles in the assembly or operation of the Neurospora circadian oscillator. Thus DNA binding and transcriptional activation can now be associated with a clock gene that may provide a positive element in the feedback loop. In addition, similarities between the PAS-domain regions of molecules involved in light perception and circadian rhythmicity in several organisms suggest an evolutionary link between ancient photoreceptor proteins and more modern proteins required for circadian oscillation.

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Year:  1997        PMID: 9115195     DOI: 10.1126/science.276.5313.763

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  155 in total

1.  Circadian clock-specific roles for the light response protein WHITE COLLAR-2.

Authors:  M A Collett; J C Dunlap; J J Loros
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

2.  Role of circadian activation of mitogen-activated protein kinase in chick pineal clock oscillation.

Authors:  K Sanada; Y Hayashi; Y Harada; T Okano; Y Fukada
Journal:  J Neurosci       Date:  2000-02-01       Impact factor: 6.167

3.  Phosphorylation of the Neurospora clock protein FREQUENCY determines its degradation rate and strongly influences the period length of the circadian clock.

Authors:  Y Liu; J Loros; J C Dunlap
Journal:  Proc Natl Acad Sci U S A       Date:  2000-01-04       Impact factor: 11.205

4.  Different period gene repeats take 'turns' at fine-tuning the circadian clock.

Authors:  V Guantieri; A Pepe; M Zordan; C P Kyriacou; R Costa; A M Tamburro
Journal:  Proc Biol Sci       Date:  1999-11-22       Impact factor: 5.349

5.  Coiled-coil domain-mediated FRQ-FRQ interaction is essential for its circadian clock function in Neurospora.

Authors:  P Cheng; Y Yang; C Heintzen; Y Liu
Journal:  EMBO J       Date:  2001-01-15       Impact factor: 11.598

6.  Loss of the circadian clock-associated protein 1 in Arabidopsis results in altered clock-regulated gene expression.

Authors:  R M Green; E M Tobin
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-30       Impact factor: 11.205

7.  Physical interactions among circadian clock proteins KaiA, KaiB and KaiC in cyanobacteria.

Authors:  H Iwasaki; Y Taniguchi; M Ishiura; T Kondo
Journal:  EMBO J       Date:  1999-03-01       Impact factor: 11.598

Review 8.  Clock-associated genes in Arabidopsis: a family affair.

Authors:  D E Somers
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2001-11-29       Impact factor: 6.237

Review 9.  Circadian systems: different levels of complexity.

Authors:  T Roenneberg; M Merrow
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2001-11-29       Impact factor: 6.237

10.  Light and clock expression of the Neurospora clock gene frequency is differentially driven by but dependent on WHITE COLLAR-2.

Authors:  Michael A Collett; Norm Garceau; Jay C Dunlap; Jennifer J Loros
Journal:  Genetics       Date:  2002-01       Impact factor: 4.562

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