Dataset Information

Positional cloning of the mouse circadian clock gene.

ABSTRACT: We used positional cloning to identify the circadian Clock gene in mice. Clock is a large transcription unit with 24 exons spanning approximately 100,000 bp of DNA from which transcript classes of 7.5 and approximately 10 kb arise. Clock encodes a novel member of the bHLH-PAS family of transcription factors. In the Clock mutant allele, an A-->T nucleotide transversion in a splice donor site causes exon skipping and deletion of 51 amino acids in the CLOCK protein. Clock is a unique gene with known circadian function and with features predicting DNA binding, protein dimerization, and activation domains. CLOCK represents the second example of a PAS domain-containing clock protein (besides Drosophila PERIOD), which suggests that this motif may define an evolutionarily conserved feature of the circadian clock mechanism.

SUBMITTER: King DP

PROVIDER: S-EPMC3815553 | biostudies-literature | 1997 May

REPOSITORIES: biostudies-literature

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Positional cloning of the mouse circadian clock gene.

King D P DP Zhao Y Y Sangoram A M AM Wilsbacher L D LD Tanaka M M Antoch M P MP Steeves T D TD Vitaterna M H MH Kornhauser J M JM Lowrey P L PL Turek F W FW Takahashi J S JS

Cell 19970501 4

We used positional cloning to identify the circadian Clock gene in mice. Clock is a large transcription unit with 24 exons spanning approximately 100,000 bp of DNA from which transcript classes of 7.5 and approximately 10 kb arise. Clock encodes a novel member of the bHLH-PAS family of transcription factors. In the Clock mutant allele, an A-->T nucleotide transversion in a splice donor site causes exon skipping and deletion of 51 amino acids in the CLOCK protein. Clock is a unique gene with know ...[more]

PMID: 9160755

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Project description:PurposeMice lacking rods and cones retain pupillary light reflexes that are mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs). Melanopsin is necessary and sufficient for this nonvisual photoreception. The mammalian inner retina also expresses the potential blue light photopigments cryptochromes 1 and 2. Previous studies have shown that outer retinal degenerate mice lacking cryptochromes have lower nonvisual photic sensitivity than retinal degenerate mice, suggesting a role for cryptochrome in inner retinal photoreception.MethodsNonvisual photoreception (pupillary light responses, circadian entrainment, and in vitro sensitivity of intrinsically photosensitive retinal ganglion cells) were studied in wild-type, rd/rd, and circadian clock-mutant mice with and without rd/rd mutation.ResultsLoss of cryptochrome in retinal degenerate mice reduces the sensitivity of the pupillary light response at all wavelengths but does not alter the form of the action spectrum, suggesting that cryptochrome does not function as a photopigment in the inner retina. The authors compounded the rd/rd retinal degeneration mutation with mutations in other essential circadian clock genes, mPeriod and Bmal1. Both mPeriod1?/?; mPeriod2?/?;rd/rd and Bmal1?/?;rd/rd mice showed significantly lower pupillary light sensitivity than rd/rd mice alone. A moderate amplitude (0.5 log) circadian rhythm of pupillary light responsiveness was observed in rd/rd mice. Multielectrode array recordings of ipRGC responses of mCryptochrome1?/?;mCryptochrome2?/? and mPeriod1?/?;mPeriod2?/? mice showed minimal sensitivity decrement compared with wild-type animals. mCryptochrome1?/?;mCryptochrome2?/?;rd/rd, mPeriod1?/?;mPeriod2?/?;rd/rd and Bmal1?/?;rd/rd mice all showed comparable weak behavioral synchronization to a 12-hour light/12-hour dark cycle.ConclusionsThe effect of cryptochrome loss on nonvisual photoreception is due to loss of the circadian clock nonspecifically. The circadian clock modulates the sensitivity of nonvisual photoreception.

Dataset Information

Positional cloning of the mouse circadian clock gene.

Publications

Positional cloning of the mouse circadian clock gene.

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