Ying-Jiun C Chen, Govinal Badiger Bhaskara, Yue Lu, Kevin Lin, Sharon Y R Dent
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Integration of RNA sequencing (RNA-seq), assay for transposase-accessible chromatin with sequencing (ATAC-seq), and cleavage under targets and release using nuclease assay (CUT&RUN) results identified pathways directly regulated by ADA2B including MTORC1 signaling and oncogenic programs driven by MYC, E2F, and MM-specific MAF. We discovered that ADA2B is recruited to MAF and MYC gene targets, and that MAF shares a majority of its targets with MYC in MM cells. Furthermore, we found that the SANT domain of ADA2B is required for interaction with both GCN5 and PCAF acetyltransferases, incorporation into SAGA, and ADA2B protein stability. 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引用次数: 0
摘要
尽管治疗方法取得了最新进展,但多发性骨髓瘤(MM)仍然是一种无法治愈的恶性肿瘤。表观遗传因素导致了多发性骨髓瘤的发病、进展、复发和克隆异质性,但我们对多发性骨髓瘤发病的表观遗传机制的了解还远远不够。SAGA 复合物是转录的辅助激活因子,可催化乙酰化和去泛素化。对癌症依赖性图谱项目数据集的分析表明,许多 SAGA 成分在 MM 中具有选择性依赖性。为了确定SAGA的特异功能,我们重点研究了ADA2B,它是赖氨酸乙酰转移酶(KAT)模块中唯一一个在SAGA中发挥特异功能的亚基。通过整合 RNA 测序(RNA-seq)、转座酶可接触染色质测序(ATAC-seq)以及靶标下裂解和核酸酶检测(CUT&RUN),我们发现了由 ADA2B 直接调控的通路,包括 MTORC1 信号传导以及由 MYC、E2F 和 MM 特异性 MAF 驱动的致癌程序。我们发现 ADA2B 被招募到 MAF 和 MYC 基因靶点,并且 MAF 与 MM 细胞中的 MYC 共享其大部分靶点。此外,我们还发现 ADA2B 的 SANT 结构域是与 GCN5 和 PCAF 乙酰转移酶相互作用、并入 SAGA 以及 ADA2B 蛋白稳定性所必需的。我们的研究结果揭示了以前未知的 SAGA KAT 模块依赖性控制 MM 细胞生长的机制,揭示了未来开发 MM 疗法时可能利用的一个弱点。
The SAGA acetyltransferase module is required for the maintenance of MAF and MYC oncogenic gene expression programs in multiple myeloma.
Despite recent advances in therapeutic treatments, multiple myeloma (MM) remains an incurable malignancy. Epigenetic factors contribute to the initiation, progression, relapse, and clonal heterogeneity in MM, but our knowledge on epigenetic mechanisms underlying MM development is far from complete. The SAGA complex serves as a coactivator in transcription and catalyzes acetylation and deubiquitylation. Analyses of data sets in the Cancer Dependency Map Project revealed that many SAGA components are selective dependencies in MM. To define SAGA-specific functions, we focused on ADA2B, the only subunit in the lysine acetyltransferase (KAT) module that specifically functions in SAGA. Integration of RNA sequencing (RNA-seq), assay for transposase-accessible chromatin with sequencing (ATAC-seq), and cleavage under targets and release using nuclease assay (CUT&RUN) results identified pathways directly regulated by ADA2B including MTORC1 signaling and oncogenic programs driven by MYC, E2F, and MM-specific MAF. We discovered that ADA2B is recruited to MAF and MYC gene targets, and that MAF shares a majority of its targets with MYC in MM cells. Furthermore, we found that the SANT domain of ADA2B is required for interaction with both GCN5 and PCAF acetyltransferases, incorporation into SAGA, and ADA2B protein stability. Our findings uncover previously unknown SAGA KAT module-dependent mechanisms controlling MM cell growth, revealing a vulnerability that might be exploited for future development of MM therapy.
期刊介绍:
Genes & Development is a research journal published in association with The Genetics Society. It publishes high-quality research papers in the areas of molecular biology, molecular genetics, and related fields. The journal features various research formats including Research papers, short Research Communications, and Resource/Methodology papers.
Genes & Development has gained recognition and is considered as one of the Top Five Research Journals in the field of Molecular Biology and Genetics. It has an impressive Impact Factor of 12.89. The journal is ranked #2 among Developmental Biology research journals, #5 in Genetics and Heredity, and is among the Top 20 in Cell Biology (according to ISI Journal Citation Reports®, 2021).