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首页> 外文期刊>Disease Prevention Daily. >Studies from University of Texas Southwestern Medical Center Dallas Yield New Information about Autoimmunity (Phosphorylation and Chromatin Tethering Prevent Cgas Activation During Mitosis)
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Studies from University of Texas Southwestern Medical Center Dallas Yield New Information about Autoimmunity (Phosphorylation and Chromatin Tethering Prevent Cgas Activation During Mitosis)

机译:研究从德克萨斯大学西南达拉斯医疗中心产生新的信息自身免疫(磷酸化和染色质有丝分裂期间拘束防止注册会计师激活)

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摘要

2021 MAY 03 (NewsRx) - By a News Reporter-Staff News Editor at Disease Prevention Daily - Data detailed on Immunology - Autoimmunity have been presented. According to news originating from Dallas, Texas, by NewsRx correspondents, research stated, "The cyclic guanosine monophosphate (GMP)-adenosine monophosphate (AMP) synthase (cGAS) detects microbial and self-DNA in the cytosol to activate immune and inflammatory programs. cGAS also associates with chromatin, especially after nuclear envelope breakdown when cells enter mitosis. How cGAS is regulated during cell cycle transition is not clear." Funders for this research include NIH National Cancer Institute (NCI), The Welch Foundation, Cancer Prevention and Research Institute of Texas, Cancer Research Institute. Our news journalists obtained a quote from the research from the University of Texas Southwestern Medical Center Dallas, "Here, we found direct biochemical evidence that cGAS activity was selectively suppressed during mitosis in human cell lines and uncovered two parallel mechanisms underlying this suppression. First, cGAS was hyperphosphorylated at the N terminus by mitotic kinases, including Aurora kinase B. The N terminus of cGAS was critical for sensing nuclear chromatin but not mitochondrial DNA. Chromatin sensing was blocked by hyperphosphorylation. Second, oligomerization of chromatin-bound cGAS, which is required for its activation, was prevented."
机译:2021年5月03 (NewsRx)——由一个新闻记者在疾病预防每日新闻编辑——数据详细的免疫学,自身免疫提出了。达拉斯,德克萨斯NewsRx记者、研究说:“环鸟苷酸(GMP)腺苷一磷酸合酶(AMP)(注册会计师)检测微生物和self-DNA胞质激活免疫和炎症项目。特别是在核膜破裂的时候细胞进入有丝分裂。细胞周期过渡并不清楚。”本研究包括国立卫生研究院国家癌症研究所(NCI),韦尔奇基金会,癌症预防和得克萨斯研究所,癌症研究所。引用的研究获得的德克萨斯大学西南医学中心达拉斯,“在这里,我们发现直接生化证据表明,海巡署活动是有选择性的在人类细胞有丝分裂线和镇压发现了两个并行机制抑制。在有丝分裂激酶的N末端,包括极光激酶b . N末端的注册会计师核染色质但不是传感的关键线粒体DNA。hyperphosphorylation。chromatin-bound的注册会计师,这需要其激活,是预防的。”

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