关贸总协定3
增强子
先天性淋巴细胞
生物
效应器
转录因子
清脆的
染色质
细胞生物学
功能(生物学)
基因
计算生物学
获得性免疫系统
遗传学
抗原
作者
Darshan N. Kasal,Zhitao Liang,Maile K. Hollinger,Crystal Y. O’Leary,Wioletta Lisicka,Anne I. Sperling,Albert Bendelac
标识
DOI:10.1073/pnas.2106311118
摘要
Significance Group 2 innate lymphoid cells (ILC2s) and adaptive CD4 + T helper type 2 (Th2) cells express a common effector program orchestrated by the “master” transcription factor GATA3 that is acquired through development or differentiation, respectively. To elucidate the regulatory mechanisms controlling the acquisition of this shared program, we used a combination of chromatin accessibility data and CRISPR/Cas9-mediated deletion, which revealed a Gata3 enhancer necessary for ILC2 development and function. Notably, this enhancer was largely dispensable for Th2 cell differentiation. Thus, ILC2s and Th2 cells display different requirements for the induction of a common type 2 helper effector program.
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