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Chromatin modifying activity of leukaemia associated fusion proteins.

机译:白血病相关融合蛋白的染色质修饰活性。

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The leukaemias, which are divided into chronic and acute forms, are malignant diseases of haematopoietic cells in which the proper balance between proliferation, differentiation and apoptosis is no longer operative. Genes, such as those of mixed-lineage leukaemia, AML1 and retinoic acid receptor alpha, have been found to be aberrantly fused to different partners, which often encode transcription factors or other chromatin modifying enzymes, in numerous types of acute lymphoid and myeloid leukaemias. These chimeric fusion oncoproteins, generated by reciprocal chromosomal translocations, are responsible for chromatin alterations on target genes whose expression is critical to stem cell development or lineage specification in haematopoiesis. Alterations in the 'histone code' or in the DNA methylation content occur as consequence of aberrant targeting of the corresponding enzymatic activities. Here, the author will review the most recent progress in the field, focusing on how fusion proteins generated by chromosomal translocation are responsible for chromatin alterations, gene deregulation and haematopoietic differentiation block and their implication for clinical treatment.
机译:分为慢性和急性形式的白血病是造血细胞的恶性疾病,其中增殖,分化和凋亡之间的适当平衡不再起作用。已经发现,在多种类型的急性淋巴细胞和髓样白血病中,诸如混合谱系白血病,AML1和视黄酸受体α的基因被异常融合到不同的伴侣上,这些伴侣通常编码转录因子或其他染色质修饰酶。这些嵌合融合癌蛋白是由相互的染色体易位产生的,负责靶基因的染色质改变,其表达对于造血干细胞发育或谱系规格至关重要。 “组蛋白密码”或DNA甲基化含量的变化是相应酶活性靶向异常的结果。在这里,作者将回顾该领域的最新进展,重点关注由染色体易位产生的融合蛋白如何引起染色质改变,基因失调和造血分化阻滞及其对临床治疗的意义。

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