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

被引:29
作者
Collett, MA
Dunlap, JC [1 ]
Loros, JJ
机构
[1] Dartmouth Med Sch, Dept Genet, Hanover, NH 03755 USA
[2] Dartmouth Med Sch, Dept Biochem, Hanover, NH 03755 USA
关键词
D O I
10.1128/MCB.21.8.2619-2628.2001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To understand the role of white collar-2 in the Neurospora circadian clock, we examined alleles of wc-2 thought to encode partially functional proteins. We found that wc-2 allele ER24 contained a conservative mutation in the zinc finger. This mutation results in reduced levels of circadian rhythm-critical clock gene products, frq mRNA and FRQ protein, and in a lengthened period of the circadian clock. In addition, this mutation altered a second canonical property of the clock, temperature compensation: as temperature increased, period length decreased substantially. This temperature compensation defect correlated with a temperature-dependent increase in overall FRQ protein levels, with the relative increase being greater in wc-2 (ER24) than in wild type, while overall frq mRNA levels were largely unaltered by temperature. We suggest that this temperature-dependent increase in FRQ levels partially rescues the lowered levels of FRQ resulting from the wc-2 (ER24) defect, yielding a shorter period at higher temperatures. Thus, normal activity of the essential clock component WC-2, a positive regulator of frq, is critical for establishing period length and temperature compensation in this circadian system.
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收藏
页码:2619 / 2628
页数:10
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