MYC增强子RNA与YEATS2蛋白的动态相互作用调控胰腺癌中MYC基因的转录

IF 6.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
EMBO Reports Pub Date : 2025-05-01 Epub Date: 2025-04-11 DOI:10.1038/s44319-025-00446-0
Jayita Roy, Aniket Kumar, Shouvik Chakravarty, Nidhan K Biswas, Srikanta Goswami, Anup Mazumder
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引用次数: 0

摘要

胰腺导管腺癌(PDAC)是最常见和侵袭性的胰腺癌之一,生存率低,治疗选择有限。MYC癌基因的异常表达促进PDAC的进展。最近的报道已经确定了增强子rna (eRNAs)的作用,起源于活性增强子,在控制基因转录。在这里,我们发现一种新的MYC eRNA在胰腺癌细胞的慢性炎症条件下调节MYC基因表达。在慢性胰腺炎和胰腺癌患者中观察到较高的MYC eRNA量。我们发现MYC eRNA与ATAC- hat复合体的组蛋白解读蛋白YEATS2相互作用,增强了含有YEATS2的ATAC复合体与MYC启动子/增强子区域的关联,从而增加了MYC基因的表达。TNF-α诱导的YEATS结构域酪氨酸去磷酸化增加胰腺癌细胞中MYC eRNA与YEATS2蛋白的结合。我们的研究通过增强子驱动的转录增加了MYC基因表达的另一个调控层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dynamic interaction of MYC enhancer RNA with YEATS2 protein regulates MYC gene transcription in pancreatic cancer.

Pancreatic ductal adenocarcinoma (PDAC) is one of the most prevalent and aggressive forms of pancreatic cancer with low survival rates and limited treatment options. Aberrant expression of the MYC oncogene promotes PDAC progression. Recent reports have established a role for enhancer RNAs (eRNAs), originating from active enhancers, in controlling gene transcription. Here we show that a novel MYC eRNA regulates MYC gene expression during chronic inflammatory conditions in pancreatic cancer cells. A higher amount of MYC eRNA is observed in chronic pancreatitis and in pancreatic cancer patients. We show that MYC eRNA interacts with YEATS2, a histone reader protein of the ATAC-HAT complex, and augments the association of YEATS2-containing ATAC complexes with MYC promoter/enhancer regions and thus increases MYC gene expression. TNF-α induced Tyrosine dephosphorylation of the YEATS domain increases MYC eRNA binding to the YEATS2 protein in pancreatic cancer cells. Our study adds another regulatory layer of MYC gene expression by enhancer-driven transcription.

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来源期刊
EMBO Reports
EMBO Reports 生物-生化与分子生物学
CiteScore
11.20
自引率
1.30%
发文量
267
审稿时长
1 months
期刊介绍: EMBO Reports is a scientific journal that specializes in publishing research articles in the fields of molecular biology, cell biology, and developmental biology. The journal is known for its commitment to publishing high-quality, impactful research that provides novel physiological and functional insights. These insights are expected to be supported by robust evidence, with independent lines of inquiry validating the findings. The journal's scope includes both long and short-format papers, catering to different types of research contributions. It values studies that: Communicate major findings: Articles that report significant discoveries or advancements in the understanding of biological processes at the molecular, cellular, and developmental levels. Confirm important findings: Research that validates or supports existing knowledge in the field, reinforcing the reliability of previous studies. Refute prominent claims: Studies that challenge or disprove widely accepted ideas or hypotheses in the biosciences, contributing to the correction and evolution of scientific understanding. Present null data: Papers that report negative results or findings that do not support a particular hypothesis, which are crucial for the scientific process as they help to refine or redirect research efforts. EMBO Reports is dedicated to maintaining high standards of scientific rigor and integrity, ensuring that the research it publishes contributes meaningfully to the advancement of knowledge in the life sciences. By covering a broad spectrum of topics and encouraging the publication of both positive and negative results, the journal plays a vital role in promoting a comprehensive and balanced view of scientific inquiry. 
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