Graduate School of Natural Science and Technology, Gifu University, 1-1 Yanagido, Gifu, 501-1193, Japan.
Department of Biomedical Sciences, College of Veterinary Medicine, King Faisal University, 31982, Al-Ahsa, Saudi Arabia.
Cell Biochem Biophys. 2024 Jun;82(2):1463-1475. doi: 10.1007/s12013-024-01300-1. Epub 2024 May 16.
Previously, we found by constructing various luciferase reporters that a well-conserved ATF6-binding element in the CRELD2 promoter is activated by transient ATF6 overexpression. In this study, we established ATF6-deficient and ATF4-deficient cell lines to analyze CRELD2 mRNA and protein expression together with that of other ER stress-inducible factors. Our results showed that ATF6 deficiency markedly suppressed tunicamycin (Tm)-induced expression of unglycosylated CRELD2. This reduction reflected a decrease in the CRELD2 transcription level. On the other hand, a putative ATF4-binding site in the mouse CRELD2 promoter did not respond to Tm stimulation, but ATF4 loss resulted in reductions in CRELD2 mRNA and protein expression, accompanied by a decrease in Tm-induced ATF6 expression. In contrast, transient suppression of GADD34, an ATF4 downstream factor, suppressed Tm-induced CRELD2 protein expression without a decrease in ATF6 protein expression. Furthermore, we investigated the association of CRELD2 with a well-known ERAD substrate, namely, an α1-antitripsin truncation mutant, NHK, by generating various CRELD2 and NHK constructs. Coimmunoprecipitation of these proteins was observed only when the cysteine in the CXXC motif on the N-terminal side of CRELD2 was replaced with alanine, and the interaction between the two was found to be disulfide bond-independent. Taken together, these findings indicate that CRELD2 expression is regulated by multiple factors via transcriptional and posttranscriptional mechanisms. In addition, the N-terminal structure of CRELD2, including the CXXC motif, was suggested to play a role in the association of the target proteins. In the future, the identification and characterization of factors interacting with CRELD2 will be useful for understanding protein homeostasis under various ER stress conditions.
先前,我们通过构建各种荧光素酶报告基因发现 CRELD2 启动子中一个高度保守的 ATF6 结合元件可被瞬时过表达的 ATF6 激活。在本研究中,我们建立了 ATF6 缺陷和 ATF4 缺陷细胞系,以分析 CRELD2mRNA 和蛋白表达以及其他内质网应激诱导因子的表达。我们的结果表明,ATF6 缺陷显著抑制了衣霉素(Tm)诱导的未糖基化 CRELD2 的表达。这种减少反映了 CRELD2 转录水平的降低。另一方面,在小鼠 CRELD2 启动子中一个假定的 ATF4 结合位点对 Tm 刺激没有反应,但 ATF4 的缺失导致 CRELD2mRNA 和蛋白表达减少,同时 Tm 诱导的 ATF6 表达减少。相反,ATF4 下游因子 GADD34 的瞬时抑制抑制了 Tm 诱导的 CRELD2 蛋白表达,而不会降低 ATF6 蛋白表达。此外,我们通过生成各种 CRELD2 和 NHK 构建体来研究 CRELD2 与一种已知的 ERAD 底物,即α1-抗胰蛋白酶截断突变体 NHK 的关联。只有当 CRELD2 氨基端CXXC 模体中的半胱氨酸被替换为丙氨酸时,才能观察到这些蛋白的共免疫沉淀,并且发现两者之间的相互作用是不依赖二硫键的。总之,这些发现表明 CRELD2 的表达受多种因素通过转录和转录后机制进行调节。此外,CRELD2 的氨基端结构,包括 CXXC 模体,被认为在靶蛋白的相互作用中起作用。在未来,与 CRELD2 相互作用的因子的鉴定和特征描述对于理解各种内质网应激条件下的蛋白质平衡将是有用的。