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ZBTB48是一种调节B细胞特异性CIITA表达的启动因子。

ZBTB48 is a priming factor regulating B-cell-specific CIITA expression.

作者信息

Rane Grishma, Kuan Vivian L S, Wang Suman, Mok Michelle Meng Huang, Khanchandani Vartika, Hansen Julia, Norvaisaite Ieva, Zulkaflee Naasyidah, Yong Wai Khang, Jahn Arne, Mukundan Vineeth T, Shi Yunyu, Osato Motomi, Li Fudong, Kappei Dennis

机构信息

Cancer Science Institute of Singapore, National University of Singapore, 117599, Singapore, Singapore.

MOE Key Laboratory for Cellular Dynamics, School of Life Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.

出版信息

EMBO J. 2024 Dec;43(24):6236-6263. doi: 10.1038/s44318-024-00306-y. Epub 2024 Nov 19.

Abstract

The class-II transactivator (CIITA) is the master regulator of MHC class-II gene expression and hence the adaptive immune response. Three cell type-specific promoters (pI, pIII, and pIV) are involved in the regulation of CIITA expression, which can be induced by IFN-γ in non-immune cells. While key regulatory elements have been identified within these promoters, our understanding of the transcription factors regulating CIITA expression is incomplete. Here, we demonstrate that the telomere-binding protein and transcriptional activator ZBTB48 directly binds to both critical activating elements within the B-cell-specific promoter CIITA pIII. ZBTB48 knockout impedes the CIITA/MHC-II expression program induced in non-APC cells by IFN-γ, and loss of ZBTB48 in mice silences MHC-II expression in pro-B and immature B cells. Transcriptional regulation of CIITA by ZBTB48 is enabled by ZBTB48-dependent chromatin opening at CIITA pIII upstream of activating H3K4me3 marks. We conclude that ZBTB48 primes CIITA pIII by acting as a molecular on-off-switch for B-cell-specific CIITA expression.

摘要

II类反式激活因子(CIITA)是MHC II类基因表达以及适应性免疫反应的主要调节因子。三种细胞类型特异性启动子(pI、pIII和pIV)参与CIITA表达的调控,CIITA表达可在非免疫细胞中被IFN-γ诱导。虽然已在这些启动子中鉴定出关键调控元件,但我们对调节CIITA表达的转录因子的了解仍不完整。在此,我们证明端粒结合蛋白及转录激活因子ZBTB48直接结合B细胞特异性启动子CIITA pIII内的两个关键激活元件。ZBTB48基因敲除会阻碍IFN-γ在非抗原呈递细胞中诱导的CIITA/MHC-II表达程序,并且小鼠中ZBTB48的缺失会使前B细胞和未成熟B细胞中的MHC-II表达沉默。ZBTB48对CIITA的转录调控是通过在激活的H3K4me3标记上游的CIITA pIII处依赖ZBTB48的染色质开放实现的。我们得出结论,ZBTB48通过作为B细胞特异性CIITA表达的分子开关来启动CIITA pIII。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/114c/11649694/f4ce97adf3e6/44318_2024_306_Fig1_HTML.jpg

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