自身免疫调节因子
生物
中心公差
染色质
组蛋白乙酰转移酶
细胞生物学
组蛋白
转录因子
乙酰化
基因
遗传学
免疫学
癌症研究
免疫耐受
抗原
作者
Melanie Heinlein,Luke C. Gandolfo,Kelin Zhao,Charis E. Teh,Nghi Nguyen,Jonathan B. Baell,Yael Goldfarb,Jakub Abramson,Johannes Wichmann,Anne K. Voss,Andreas Strasser,Gordon K. Smyth,Tim Thomas,Daniel H.D. Gray
出处
期刊:PubMed
日期:2022-01-21
卷期号:7 (67): eabb6032-eabb6032
被引量:9
标识
DOI:10.1126/sciimmunol.abb6032
摘要
The autoimmune regulator (AIRE) induces the transcription of thousands of peripheral tissue genes (PTGs) in thymic epithelial cells (TECs) to mediate immunological tolerance. The chromatin state required for optimal AIRE function in TECs and how this state is induced remains unclear. We tested the role of the histone acetyltransferase, KAT7 (also known as HBO1 or MYST2), which is essential for acetylation of histone 3 lysine 14, in TEC differentiation, AIRE-mediated PTG expression, and thymic tolerance. We find that KAT7 is required for optimal expansion of medullary TEC and has a major role in the expression of AIRE-dependent PTGs, associated with enhanced chromatin accessibility at these gene loci in TECs. Mice with TEC-specific Kat7 deletion develop organ-specific autoimmunity with features resembling those observed in Aire-deficient mice. These findings highlight critical roles for KAT7-mediated acetylation in promoting a chromatin state at PTG loci that enables AIRE function and the establishment of immunological tolerance.
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