氨酸/NFATc1通路通过调节 histone H3 表达抑制细胞细胞毒性
Yuki Sato1, Makoto Habara1, Shunsuke Hanaki1
1Department of Veterinary Biochemistry, Joint Faculty of Veterinary Medicine, Yamaguchi University, 1677-1 Yoshida, Yamaguchi, 753-8511, Japan.
Scientific reports
|June 26, 2024
概括
过多的质子会导致基因组的不稳定. 转录因子NFATc1 (激活T细胞1的核因子) 抑制了组质素基因表达,防止有害的组质素积累并维持细胞存活.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 遗传学 遗传学 是一个
背景情况:
- 过量的组织蛋白导致线粒染色体损失和基因组不稳定,威胁到细胞的生存.
- 酵母菌中的质子降解涉及蛋白酶和Rad53,但转录调节仍然不清楚.
研究的目的:
- 为了研究基因基因的转录调节.
- 识别控制基因组表达的因素及其在预防基因组不稳定中的作用.
主要方法:
- 用氨酸抑制剂进行治疗.
- 对转录因子NFATc1结合基因组基因促进体的分析.
- 对细胞内水平的反应中基因表达的评估.
- 细胞增殖测定基因组H3过度表达.
主要成果:
- 卡尔西纽林抑制剂治疗导致基因组蛋白水平升高.
- 鉴定出NFATc1是组织素转录的抑制剂,作用于尿的下游.
- NFATc1结合到多个组素基因的促销者.
- 基斯转录由细胞内水平下调.
- 过度表达的希斯H3显著损害了细胞增殖.
结论:
- NFATc1在防止有害的组织激素积累方面发挥着至关重要的作用.
- NFATc1通过压制基因表达的转录来维持基因组的稳定性.
- 细胞内水平通过NFATc1.1调节组织素转录.
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