ISOLATION OF TIMELESS BY PER PROTEIN-INTERACTION - DEFECTIVE INTERACTION BETWEEN TIMELESS PROTEIN AND LONG-PERIOD MUTANT PER(L)

被引:307
作者
GEKAKIS, N
SAEZ, L
DELAHAYEBROWN, AM
MYERS, MP
SEHGAL, A
YOUNG, MW
WEITZ, CJ
机构
[1] HARVARD UNIV, SCH MED, DEPT NEUROBIOL, BOSTON, MA 02115 USA
[2] ROCKEFELLER UNIV, CTR BIOL TIMING, HOWARD HUGHES MED INST, NATL SCI FDN SCI & TECHNOL, NEW YORK, NY 10021 USA
[3] ROCKEFELLER UNIV, GENET LAB, NEW YORK, NY 10021 USA
[4] UNIV PENN, MED CTR, DEPT NEUROSCI, PHILADELPHIA, PA 19104 USA
[5] UNIV PENN, MED CTR, CTR SLEEP & RESP NEUROBIOL, PHILADELPHIA, PA 19104 USA
关键词
D O I
10.1126/science.270.5237.811
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The period (per) gene likely encodes a component of the Drosophila circadian clock. Circadian oscillations in the abundance of per messenger RNA and per protein (PER) are thought to arise from negative feedback control of per gene transcription by PER. A recently identified second clock locus, timeless (tim), apparently regulates entry of PER into the nucleus. Reported here are the cloning of complementary DNAs derived from the tim gene in a two-hybrid screen for PER-interacting proteins and the demonstration of a physical interaction between the tim protein (TIM) and PER in vitro. A restricted segment of TIM binds directly to a part of the PER dimerization domain PAS. PER(L), a mutation that causes a temperature-sensitive lengthening of circadian period and a temperature-sensitive delay in PER nuclear entry, exhibits a temperature-sensitive defect in binding to TIM. These results suggest that the interaction between TIM and PER determines the timing of PER nuclear entry and therefore the duration of part of the circadian cycle.
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页码:811 / 815
页数:5
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