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热休克蛋白 90B 基因(HSP90B)在模式单细胞绿藻衣藻中的基因表达和启动子特征。

Gene expression and promoter characterization of heat-shock protein 90B gene (HSP90B) in the model unicellular green alga Chlamydomonas reinhardtii.

机构信息

Department of Biochemistry, Faculty of Science, Mahidol University, 272 Rama 6 Rd., Bangkok 10400, Thailand; Center for Excellence in Protein and Enzyme Technology, Faculty of Science, Mahidol University, 272 Rama 6 Rd., Bangkok 10400, Thailand.

Department of Biochemistry, Faculty of Science, Kasetsart University, 50 Ngamwongwan Rd., Bangkok 10900, Thailand.

出版信息

Plant Sci. 2018 Jul;272:107-116. doi: 10.1016/j.plantsci.2018.04.010. Epub 2018 Apr 17.

Abstract

Molecular chaperones or heat shock proteins are a large protein family with important functions in every cellular organism. Among all types of the heat shock proteins, information on the ER-localized HSP90 protein (HSP90B) and its encoding gene is relatively scarce in the literature, especially in photosynthetic organisms. In this study, expression profiles as well as promoter sequence of the HSP90B gene were investigated in the model green alga Chlamydomonas reinhardtii. We have found that HSP90B is strongly induced by heat and ER stresses, while other short-term exposure to abiotic stresses, such as salinity, dark-to-light transition or light stress does not appear to affect the expression. Promoter truncation analysis as well as chromatin immunoprecipitation using the antibodies recognizing histone H3 and acetylated histone H3, revealed a putative core constitutive promoter sequence between -1 to -253 bp from the transcription start site. Our results also suggested that the nucleotides upstream of the core promoter may contain repressive elements such as putative repressor binding site(s).

摘要

分子伴侣或热休克蛋白是一个具有重要功能的大型蛋白质家族,存在于每一种细胞生物中。在所有类型的热休克蛋白中,关于内质网定位的 HSP90 蛋白(HSP90B)及其编码基因的信息在文献中相对较少,尤其是在光合生物中。在这项研究中,我们研究了模式绿藻莱茵衣藻中 HSP90B 基因的表达谱和启动子序列。我们发现 HSP90B 强烈地受到热激和内质网应激的诱导,而其他短期的非生物应激,如盐度、暗转光或光应激,似乎并不影响其表达。启动子截断分析以及使用识别组蛋白 H3 和乙酰化组蛋白 H3 的抗体进行的染色质免疫沉淀实验,揭示了一个位于转录起始位点前 -1 到 -253bp 的推定核心组成型启动子序列。我们的结果还表明,核心启动子上游的核苷酸可能包含抑制元件,如推定的抑制因子结合位点。

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