Circadian clock genes reign in duration of fruit fly ...( This week researchers at Oregon State ...)

This week, researchers at Oregon State University report evidence that two genes representing key components of the circadian clock somehow also influence sexual behavior in the fruit fly Drosophila. Circadian rhythms control the timing of physiological events over the course of day-night cycles approximating 24 hours. The new work reveals that, in fact, at least some circadian clock genes can also control the duration of behaviors over a much shorter time scale--in this case, the length of the fly's copulation. The effects on copulation are independent of light and the 24-hour circadian clock.

The researchers reporting the work, Laura Beaver and Dr. Jaga Giebultowicz, found that male flies lacking one of two circadian clock genes, "period" or "timeless," exhibited an altered sexual behavior in which copulation time was significantly extended. Whereas copulation normally lasts for around 15 minutes, males carrying mutations in period or timeless spent up to 3050% more time in copulation than their normal male counterparts. The effect is sex-specific, because mutant female flies copulating with normal males did not show a similar change in behavior.

Both the period and timeless genes are evolutionarily conserved components of the molecular circadian clock mechanism and are present in diverse species including humans. Both genes play critical roles in the control of the 24-hour clock. However, despite their roles in controlling the timing of daily behaviors such as sleep, the period and timeless genes appear to influence the duration of fly copulation through a mechanism that is separate from the daily circadian clock. The researchers found, for example, that altered oscillations of the circadian clock do not affect the flies' time in copulation and neither does constant light, which abolishes the clock function. Together, the new findings broaden the known set of behaviors controlled by the period and timeless genes and suggest that these genes might
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Contact: Heidi Hardman
hhardman@cell.com
617-397-2879
Cell Press
23-Aug-2004

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