Spatial and circadian regulation of cry in Drosophila.

J Biol Rhythms

Department of Biology and Center for Research on Biological Clocks, Texas A&M University, College Station, TX 77843-3258, USA.

Published: August 2008

AI Article Synopsis

  • In Drosophila, cryptochrome (cry) acts as a blue-light photoreceptor essential for circadian rhythm regulation and its mRNA levels cycle, peaking around ZT5, similar to Clock (Clk) mRNA.
  • A research study employed various cry-Gal4 trans-genes with different cry sequences to analyze the regulation of cry's spatial and circadian expression.
  • Findings indicate that cry upstream sequences promote steady expression in brain and peripheral oscillator cells, while intron 1 ensures rhythmic expression specifically in eyes and antennae, revealing distinct regulatory elements for spatial and circadian expression.

Article Abstract

In Drosophila, cryptochrome (cry) encodes a blue-light photoreceptor that mediates light input to circadian oscillators and sustains oscillator function in peripheral tissues. The levels of cry mRNA cycle with a peak at approximately ZT5, which is similar to the phase of Clock (Clk) mRNA cycling in Drosophila. To understand how cry spatial and circadian expression is regulated, a series of cry-Gal4 trans-genes containing different portions of cry upstream and intron 1 sequences were tested for spatial and circadian expression. In fly heads, cry upstream sequences drive constitutive expression in brain oscillator neurons, a novel group of nonoscillator cells in the optic lobe, and peripheral oscillator cells in eyes and antennae. In contrast, cry intron 1 drives rhythmic expression in eyes and antennae, but not brain oscillator neurons. These results demonstrate that intron 1 is sufficient for high-amplitude cry mRNA cycling, show that cry upstream sequences are sufficient for expression in brain oscillator neurons, and suggest that cry spatial and circadian expression are regulated by different elements.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2504742PMC
http://dx.doi.org/10.1177/0748730408318566DOI Listing

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