Suppr超能文献

11q23 重排和 t(8;16) 急性髓系白血病中 C 端 BRE 的过表达是由基因内转录起始引起的。

C-terminal BRE overexpression in 11q23-rearranged and t(8;16) acute myeloid leukemia is caused by intragenic transcription initiation.

机构信息

Department of Laboratory Medicine, Laboratory of Hematology, Radboud Institute for Molecular Life Sciences (RIMLS), Radboud University Medical Center, Nijmegen, The Netherlands.

Department of Molecular Biology, Faculty of Science, RIMLS, Radboud University, Nijmegen, The Netherlands.

出版信息

Leukemia. 2018 Mar;32(3):828-836. doi: 10.1038/leu.2017.280. Epub 2017 Sep 5.

Abstract

Overexpression of the BRE (brain and reproductive organ-expressed) gene defines a distinct pediatric and adult acute myeloid leukemia (AML) subgroup. Here we identify a promoter enriched for active chromatin marks in BRE intron 4 causing strong biallelic expression of a previously unknown C-terminal BRE transcript. This transcript starts with BRE intron 4 sequences spliced to exon 5 and downstream sequences, and if translated might code for an N terminally truncated BRE protein. Remarkably, the new BRE transcript was highly expressed in over 50% of 11q23/KMT2A (lysine methyl transferase 2A)-rearranged and t(8;16)/KAT6A-CREBBP cases, while it was virtually absent from other AML subsets and normal tissues. In gene reporter assays, the leukemia-specific fusion protein KMT2A-MLLT3 transactivated the intragenic BRE promoter. Further epigenome analyses revealed 97 additional intragenic promoter marks frequently bound by KMT2A in AML with C-terminal BRE expression. The corresponding genes may be part of a context-dependent KMT2A-MLLT3-driven oncogenic program, because they were higher expressed in this AML subtype compared with other groups. C-terminal BRE might be an important contributor to this program because in a case with relapsed AML, we observed an ins(11;2) fusing CHORDC1 to BRE at the region where intragenic transcription starts in KMT2A-rearranged and KAT6A-CREBBP AML.

摘要

BRE(脑和生殖器官表达)基因的过表达定义了一个独特的儿科和成人急性髓系白血病(AML)亚组。在这里,我们确定了一个在 BRE 内含子 4 中富含活性染色质标记的启动子,导致以前未知的 C 末端 BRE 转录本的强烈双等位基因表达。这种转录本从 BRE 内含子 4 序列拼接的外显子 5 和下游序列开始,如果翻译,可能编码一个 N 端截断的 BRE 蛋白。值得注意的是,新的 BRE 转录本在超过 50%的 11q23/KMT2A(赖氨酸甲基转移酶 2A)重排和 t(8;16)/KAT6A-CREBBP 病例中高度表达,而在其他 AML 亚组和正常组织中几乎不存在。在基因报告基因实验中,白血病特异性融合蛋白 KMT2A-MLLT3 反式激活基因内的 BRE 启动子。进一步的表观基因组分析显示,在具有 C 末端 BRE 表达的 AML 中,97 个额外的基因内启动子标记经常被 KMT2A 结合。相应的基因可能是一个依赖于上下文的 KMT2A-MLLT3 驱动的致癌程序的一部分,因为与其他组相比,它们在这种 AML 亚型中表达更高。C 末端 BRE 可能是该程序的一个重要贡献者,因为在一个复发的 AML 病例中,我们观察到一个 ins(11;2) 将 CHORDC1 融合到 BRE,在 KMT2A 重排和 KAT6A-CREBBP AML 中,基因内转录开始的区域。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验