染色质
辅活化剂
同源盒
pou结构域
增强子
生物
癌症研究
基因
遗传学
转录因子
细胞生物学
作者
Aileen P. Szczepanski,Natsumi Tsuboyama,Jun Watanabe,Rintaro Hashizume,Zibo Zhao,Lu Wang
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2022-10-07
卷期号:8 (40)
被引量:13
标识
DOI:10.1126/sciadv.abq2403
摘要
Small cell lung cancer (SCLC), accounting for around 13% of all lung cancers, often results in rapid tumor growth, early metastasis, and acquired therapeutic resistance. The POU class 2 homeobox 3 (POU2F3) is a master regulator of tuft cell identity and defines the SCLC-P subtype that lacks the neuroendocrine markers. Here, we have identified a previously uncharacterized protein, C11orf53, which is coexpressed with POU2F3 in both SCLC cell lines and patient samples. Mechanistically, C11orf53 directly interacts with POU2F3 and is recruited to chromatin by POU2F3. Depletion of C11orf53 reduced enhancer H3K27ac levels and chromatin accessibility, resulting in a reduction of POU2F3-dependent gene expression. On the basis of the molecular function of C11orf53, we renamed it as "POU Class 2 Homeobox Associating Factor 2" (POU2AF2). In summary, our study has identified a new coactivator of POU2F3 and sheds light on the therapeutic potential of targeting POU2AF2/POU2F3 heterodimer in human SCLC.
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