Abstract

BackgroundWHITE COLLAR-1 (WC-1) mediates interactions between the circadian clock and the environment by acting as both a core clock component and as a blue light photoreceptor in Neurospora crassa. Loss of the amino-terminal polyglutamine (NpolyQ) domain in WC-1 results in an arrhythmic circadian clock; this data is consistent with this simple sequence repeat (SSR) being essential for clock function.Methodology/Principal FindingsSince SSRs are often polymorphic in length across natural populations, we reasoned that investigating natural variation of the WC-1 NpolyQ may provide insight into its role in the circadian clock. We observed significant phenotypic variation in the period, phase and temperature compensation of circadian regulated asexual conidiation across 143 N. crassa accessions. In addition to the NpolyQ, we identified two other simple sequence repeats in WC-1. The sizes of all three WC-1 SSRs correlated with polymorphisms in other clock genes, latitude and circadian period length. Furthermore, in a cross between two N. crassa accessions, the WC-1 NpolyQ co-segregated with period length.Conclusions/SignificanceNatural variation of the WC-1 NpolyQ suggests a mechanism by which period length can be varied and selected for by the local environment that does not deleteriously affect WC-1 activity. Understanding natural variation in the N. crassa circadian clock will facilitate an understanding of how fungi exploit their environments.

Highlights

  • Circadian clocks are internal timing mechanisms found across all kingdoms that synchronize the biological process of an organism with its local environment [1,2,3]

  • We established that the natural period length of the N. crassa circadian clock is 22 hours, two hours shorter than the external period of daily light and temperature cycles

  • We genetically separated the WHITE COLLAR-1 (WC-1) and FRQ alleles and demonstrated that the simple sequence repeat (SSR) polymorphism in WC-1 accounted for the period phenotype (Figure 5)

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Summary

Introduction

Circadian clocks are internal timing mechanisms found across all kingdoms that synchronize the biological process of an organism with its local environment [1,2,3]. Entrainment to the ambient 24 hour period partitions biological processes to the correct time of day, or phase, in relation to environmental cues. It is important for the circadian clock to maintain a constant period over a range of physiological temperatures; the clock is temperature compensated and its temperature coefficient (Q10) is lower than normal enzymatic reactions [4]. Understanding natural variation in the N. crassa circadian clock will facilitate an understanding of how fungi exploit their environments

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