生物
染色体易位
白血病
髓系白血病
融合基因
癌症研究
表观遗传学
组蛋白乙酰转移酶
基因
遗传学
作者
Kazutsune Yamagata,Mika Shino,Yukiko Aikawa,Shuhei Fujita,Issay Kitabayashi
出处
期刊:Leukemia
[Springer Nature]
日期:2021-05-09
卷期号:35 (10): 2840-2853
被引量:14
标识
DOI:10.1038/s41375-021-01244-y
摘要
Chromosome translocations involving the MLL gene are common rearrangements in leukemia. Such translocations fuse the MLL 5'-region to partner genes in frame, producing MLL-fusions that cause MLL-related leukemia. MLL-fusions activate transcription of target genes such as HoxA cluster and Meis1, but the underlying mechanisms remain to be fully elucidated. In this study, we discovered that Tip60, a MYST-type histone acetyltransferase, was required for the expression of HoxA cluster and Meis1 genes and the development of MLL-fusion leukemia. Tip60 was recruited by MLL-AF10 and MLL-ENL fusions to the Hoxa9 locus, where it acetylated H2A.Z, thereby promoting Hoxa9 gene expression. Conditional deletion of Tip60 prevented the development of MLL-AF10 and MLL-ENL leukemia, indicating that Tip60 is indispensable for the leukemogenic activity of the MLL-AF10 and MLL-ENL-fusions. Our findings provide novel insight about epigenetic regulation in the development of MLL-AF10 and MLL-ENL-fusion leukemia.
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