在t细胞急性淋巴细胞白血病中,PHF6与LMO2复合物相互作用。

IF 7.9 1区 医学 Q1 HEMATOLOGY
Vesna S Stanulović,Sarah Binhassan,Budoor A Jaber,Shimaa Alazmi,Fatma M B Saleman,Sandeep Potluri,Guy Pratt,Christian Ludwig,Douglas G Ward,Maarten Hoogenkamp
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引用次数: 0

摘要

转录介质LIM domain only 2 (LMO2)与TAL1/LYL1、HEB/E2A、LDB1和GATA形成一个大的多蛋白复合物。这个复合体从造血发育开始和分化过程中调控转录。涉及LMO2和TAL1的染色体重排是t细胞淋巴母细胞白血病(TALL)的病因。我们已经鉴定出Plant Homeodomain (PHD)- likefinger 6 (PHF6)是一个新的LMO2相互作用因子。已经发现PHF6的体细胞突变发生在几种类型的白血病中。我们发现PHF6作为T-ALL中TAL1, GATA2, LDB1复合体的一部分与LMO2相互作用并结合到DNA上。这些发现表明,PHF6与TAL1/LMO2/LDB1/GATA2复合体相关,并调节在血液发育中起主要作用的基因,如SPI1 (PU.1)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PHF6 interacts with the LMO2 complex in T-cell acute lymphoblastic leukemia.
The transcriptional mediator LIM domain only 2 (LMO2) forms a large multi-protein complex together with TAL1/LYL1, HEB/E2A, LDB1 and GATA. This complex regulates transcription from the onset of hematopoietic development and during differentiation. Chromosomal rearrangements involving LMO2 and TAL1 are causative for T-cell lymphoblastic leukemia (TALL). We have identified Plant Homeodomain (PHD)-like Finger 6 (PHF6) as a new LMO2 interacting factor. Somatic mutations in PHF6 have been found to occur in several types of leukemia. We show that PHF6 interacts with LMO2 as a part of the TAL1, GATA2, LDB1 complex in T-ALL and binds to the DNA. These findings show that PHF6 associates with the TAL1/LMO2/LDB1/GATA2 complex and regulates genes that have a major role in blood development, such as SPI1 (PU.1).
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来源期刊
Haematologica
Haematologica 医学-血液学
CiteScore
14.10
自引率
2.00%
发文量
349
审稿时长
3-6 weeks
期刊介绍: Haematologica is a journal that publishes articles within the broad field of hematology. It reports on novel findings in basic, clinical, and translational research. Scope: The scope of the journal includes reporting novel research results that: Have a significant impact on understanding normal hematology or the development of hematological diseases. Are likely to bring important changes to the diagnosis or treatment of hematological diseases.
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