Kume K, Zylka M J, Sriram S, Shearman L P, Weaver D R, Jin X, Maywood E S, Hastings M H, Reppert S M
Laboratory of Developmental Chronobiology, Pediatric Service, Massachusetts General Hospital and Harvard Medical School, Boston 02114, USA.
Cell. 1999 Jul 23;98(2):193-205. doi: 10.1016/s0092-8674(00)81014-4.
We determined that two mouse cryptochrome genes, mCry1 and mCry2, act in the negative limb of the clock feedback loop. In cell lines, mPER proteins (alone or in combination) have modest effects on their cellular location and ability to inhibit CLOCK:BMAL1 -mediated transcription. This suggested cryptochrome involvement in the negative limb of the feedback loop. Indeed, mCry1 and mCry2 RNA levels are reduced in the central and peripheral clocks of Clock/Clock mutant mice. mCRY1 and mCRY2 are nuclear proteins that interact with each of the mPER proteins, translocate each mPER protein from cytoplasm to nucleus, and are rhythmically expressed in the suprachiasmatic circadian clock. Luciferase reporter gene assays show that mCRY1 or mCRY2 alone abrogates CLOCK:BMAL1-E box-mediated transcription. The mPER and mCRY proteins appear to inhibit the transcriptional complex differentially.
我们确定,小鼠的两个隐花色素基因mCry1和mCry2在生物钟反馈回路的负向分支中起作用。在细胞系中,mPER蛋白(单独或联合)对其细胞定位以及抑制CLOCK:BMAL1介导的转录的能力有适度影响。这表明隐花色素参与了反馈回路的负向分支。实际上,在Clock/Clock突变小鼠的中枢和外周生物钟中,mCry1和mCry2的RNA水平降低。mCRY1和mCRY2是核蛋白,它们与每个mPER蛋白相互作用,将每个mPER蛋白从细胞质转运到细胞核,并在视交叉上昼夜节律生物钟中有节律地表达。荧光素酶报告基因检测表明,单独的mCRY1或mCRY2可消除CLOCK:BMAL1-E盒介导的转录。mPER和mCRY蛋白似乎对转录复合物有不同的抑制作用。