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Inflammatory Response: USP38 Couples Histone Ubiquitination and Methylation via KDM5B to Resolve Inflammation (Adv. Sci. 22/2020)

机译:炎症反应:USP38通过KDM5B将组蛋白泛素化和甲基化致致抗炎(ADV。SCI。22/2020)

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In article number 2002680, Jun Cui and co‐workers identify a new histone modifier‐USP38, that modulates histone ubiquitination and methylation to resolve inflammatory response. USP38 acts as a “Safety Machine” which shuts down the inflammation by de‐ubiquitinating histone H2B and stabilizes KDM5B to de‐methylate H3K4, which blocks the transcription of pro‐inflammatory genes. The USP38‐KDM5B complex might be a potential clinical target for therapy against inflammatory diseases.
机译:在2002680年,Jun Cui和同官员中鉴定了一种新的组蛋白改性剂-USP38,其调节组蛋白泛素化和甲基化以解决炎症反应。 USP38充当“安全机器”,其通过去ubiquitinated组蛋白H2b关闭炎症,并稳定KDM5B至去甲基化物H3K4,其阻断促炎基因的转录。 USP38-KDM5B复合物可能是对炎症性疾病进行治疗的潜在临床目标。

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