Abstract 2118: Non-coding germline GATA3 variants alter chromatin topology and contribute to pathogenesis of acute lymphoblastic leukemia

Hongbo Yang, Hui Zhang, Yu Luan, Tingting Liu, K. Roberts, Maoxiang Qian, Bo Zhang, Wenjian Yang, V. Pérez-Andreu, Jie Xu, Sriranga lyyanki, Da Kuang, S. Reshmi, J. Gastier-Foster, Colton A. Smith, C. Pui, W. Evans, S. Hunger, L. Platanias, M. Relling, C. Mullighan, M. Loh, Feng Yue, Jun J. Yang
{"title":"Abstract 2118: Non-coding germline GATA3 variants alter chromatin topology and contribute to pathogenesis of acute lymphoblastic leukemia","authors":"Hongbo Yang, Hui Zhang, Yu Luan, Tingting Liu, K. Roberts, Maoxiang Qian, Bo Zhang, Wenjian Yang, V. Pérez-Andreu, Jie Xu, Sriranga lyyanki, Da Kuang, S. Reshmi, J. Gastier-Foster, Colton A. Smith, C. Pui, W. Evans, S. Hunger, L. Platanias, M. Relling, C. Mullighan, M. Loh, Feng Yue, Jun J. Yang","doi":"10.1158/1538-7445.AM2021-2118","DOIUrl":null,"url":null,"abstract":"Inherited non-coding genetic variants confer significant disease susceptibility in many cancers. However, the molecular processes of by which germline variants contribute to somatic lesions are poorly understood. We performed targeted sequencing in 5,008 patients and identified a key regulatory germline variant in GATA3 strongly associated with Philadelphia chromosome-like acute lymphoblastic leukemia (Ph-like ALL). By creating an isogenic cellular model with CRISPR-Cas9 system, we showed that this variant activated a strong enhancer that significantly upregulated GATA3 transcription, which in turn reshaped the global chromatin accessibility and 3D genome organization. Remarkably, this genotype switch induced a chromatin loop between the CRLF2 oncogene and a distal enhancer, similar to the somatically acquired super-enhancer hijacking event in patients. GATA3 genotype-related alterations in transcriptional control and 3D chromatin organization were further validated in Ph-like ALL patients. Finally, we showed that GATA3 directly regulates CRLF2 and potentiates the oncogenic effects of JAK-STAT signaling in leukemogenesis. Altogether, our results provide evidence for a novel mechanism by which a germline non-coding variant contributes to oncogene activation epigenetic regulation and 3D genome reprogramming. Citation Format: Hongbo Yang, Hui Zhang, Yu Luan, Tingting Liu, Kathryn Roberts, Mao-xiang Qian, Bo Zhang, Wenjian Yang, Virginia Perez-Andreu, Jie Xu, Sriranga lyyanki, Da Kuang, Shalini Reshmi, Julie Gastier-Foster, Colton Smith, Ching-Hon Pui, William Evans, Stephen Hunger, Stephen Hunger, Leonidas Platanias, Mary Relling, Charles Mullighan, Mignon Loh, Feng Yue, Jun Yang. Non-coding germline GATA3 variants alter chromatin topology and contribute to pathogenesis of acute lymphoblastic leukemia [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2118.","PeriodicalId":18754,"journal":{"name":"Molecular and Cellular Biology / Genetics","volume":"26 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular and Cellular Biology / Genetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1158/1538-7445.AM2021-2118","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Inherited non-coding genetic variants confer significant disease susceptibility in many cancers. However, the molecular processes of by which germline variants contribute to somatic lesions are poorly understood. We performed targeted sequencing in 5,008 patients and identified a key regulatory germline variant in GATA3 strongly associated with Philadelphia chromosome-like acute lymphoblastic leukemia (Ph-like ALL). By creating an isogenic cellular model with CRISPR-Cas9 system, we showed that this variant activated a strong enhancer that significantly upregulated GATA3 transcription, which in turn reshaped the global chromatin accessibility and 3D genome organization. Remarkably, this genotype switch induced a chromatin loop between the CRLF2 oncogene and a distal enhancer, similar to the somatically acquired super-enhancer hijacking event in patients. GATA3 genotype-related alterations in transcriptional control and 3D chromatin organization were further validated in Ph-like ALL patients. Finally, we showed that GATA3 directly regulates CRLF2 and potentiates the oncogenic effects of JAK-STAT signaling in leukemogenesis. Altogether, our results provide evidence for a novel mechanism by which a germline non-coding variant contributes to oncogene activation epigenetic regulation and 3D genome reprogramming. Citation Format: Hongbo Yang, Hui Zhang, Yu Luan, Tingting Liu, Kathryn Roberts, Mao-xiang Qian, Bo Zhang, Wenjian Yang, Virginia Perez-Andreu, Jie Xu, Sriranga lyyanki, Da Kuang, Shalini Reshmi, Julie Gastier-Foster, Colton Smith, Ching-Hon Pui, William Evans, Stephen Hunger, Stephen Hunger, Leonidas Platanias, Mary Relling, Charles Mullighan, Mignon Loh, Feng Yue, Jun Yang. Non-coding germline GATA3 variants alter chromatin topology and contribute to pathogenesis of acute lymphoblastic leukemia [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2118.
非编码种系GATA3变异改变染色质拓扑结构并参与急性淋巴细胞白血病的发病机制
遗传性非编码基因变异赋予许多癌症显著的疾病易感性。然而,由种系变异导致体细胞病变的分子过程尚不清楚。我们对5008例患者进行了靶向测序,发现了GATA3中一个与费城染色体样急性淋巴细胞白血病(Ph-like ALL)密切相关的关键调节种系变异。通过使用CRISPR-Cas9系统创建等基因细胞模型,我们发现该变体激活了一个强增强子,显著上调GATA3转录,从而重塑了全球染色质可及性和3D基因组组织。值得注意的是,这种基因型开关诱导了CRLF2癌基因和远端增强子之间的染色质环,类似于患者体内获得的超级增强子劫持事件。在ph样ALL患者中进一步验证了转录控制和3D染色质组织中GATA3基因型相关的改变。最后,我们发现GATA3直接调节CRLF2并增强JAK-STAT信号在白血病发生中的致癌作用。总之,我们的研究结果为种系非编码变异参与癌基因激活、表观遗传调控和3D基因组重编程的新机制提供了证据。引文格式:杨洪波、张辉、栾宇、刘婷婷、Kathryn Roberts、钱茂翔、张博、杨文健、Virginia Perez-Andreu、徐杰、Sriranga lyyanki、Da Kuang、Shalini Reshmi、Julie Gastier-Foster、Colton Smith、puching - hon、William Evans、Stephen Hunger、Stephen Hunger、Leonidas Platanias、Mary Relling、Charles Mullighan、Mignon Loh、Feng Yue、Yang Jun。非编码种系GATA3变异改变染色质拓扑结构,参与急性淋巴细胞白血病的发病机制[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):2118。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信