Ohno Tomoya, Onishi Yoshiaki, Ishida Norio
Clock Cell Biology, Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology, Central 6-5, 1-1-1 Higashi, Tsukuba, Japan.
Biochem Biophys Res Commun. 2007 Mar 23;354(4):1010-5. doi: 10.1016/j.bbrc.2007.01.084. Epub 2007 Jan 24.
The bZIP transcription factor E4BP4, is a mammalian homologue of vrille that functions as a key negative component of the circadian clock. We have shown that the E4BP4-binding site (B-site) is required in addition to a non-canonical E-box (E2 enhancer) for robust circadian Period2 (Per2) expression in the cell-autonomous clock. While the E2 enhancer and the B-site are closely situated, correlations between each component bound to the E2 enhancer and the B-site remain obscure. Here, we show that E4BP4 interacts with PER2, which represses transcriptional activity via the E-box enhancer. Interaction with PER2 required the carboxyl-terminal region that contains the repression domain of E4BP4. We also found that E4BP4 interacts with CRYPTOCHROME2 (CRY2), a key negative regulator in the mammalian circadian clock. These results suggest that E4BP4 is a component of the negative regulator complex of mammalian circadian clocks.
碱性亮氨酸拉链转录因子E4BP4是果蝇生物钟蛋白vrille的哺乳动物同源物,在生物钟中作为关键的负调控因子发挥作用。我们已经表明,除了非典型E盒(E2增强子)之外,E4BP4结合位点(B位点)对于细胞自主生物钟中强大的昼夜节律Period2(Per2)表达也是必需的。虽然E2增强子和B位点紧密相邻,但与E2增强子和B位点结合的每个组分之间的相关性仍不清楚。在这里,我们表明E4BP4与PER2相互作用,后者通过E盒增强子抑制转录活性。与PER2的相互作用需要包含E4BP4抑制结构域的羧基末端区域。我们还发现E4BP4与哺乳动物生物钟中的关键负调控因子隐花色素2(CRY2)相互作用。这些结果表明E4BP4是哺乳动物生物钟负调控复合物的一个组分。