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白血病中表观遗传修饰的动力学。

Dynamics of epigenetic modifications in leukemia.

机构信息

Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona 08003, Spain.

出版信息

Brief Funct Genomics. 2011 Jan;10(1):18-29. doi: 10.1093/bfgp/elr002. Epub 2011 Jan 21.

Abstract

Chromatin modifications at both histones and DNA are critical for regulating gene expression. Mis-regulation of such epigenetic marks can lead to pathological states; indeed, cancer affecting the hematopoietic system is frequently linked to epigenetic abnormalities. Here, we discuss the different types of modifications and their general impact on transcription, as well as the polycomb group of proteins, which effect transcriptional repression and are often mis-regulated. Further, we discuss how chromosomal translocations leading to fusion proteins can aberrantly regulate gene transcription through chromatin modifications within the hematopoietic system. PML-RARa, AML1-ETO and MLL-fusions are examples of fusion proteins that mis-regulate epigenetic modifications (either directly or indirectly), which can lead to acute myeloblastic leukemia (AML). An in-depth understanding of the mechanisms behind the mis-regulation of epigenetic modifications that lead to the development and progression of AMLs could be critical for designing effective treatments.

摘要

染色质修饰在组蛋白和 DNA 上对于调节基因表达至关重要。这种表观遗传标记的失调可能导致病理状态;事实上,影响造血系统的癌症通常与表观遗传异常有关。在这里,我们讨论了不同类型的修饰及其对转录的一般影响,以及多梳蛋白组蛋白,其影响转录抑制,并且经常失调。此外,我们还讨论了导致融合蛋白的染色体易位如何通过造血系统内的染色质修饰异常调节基因转录。PML-RARa、AML1-ETO 和 MLL 融合蛋白是异常调节表观遗传修饰(直接或间接)的融合蛋白的例子,可导致急性髓细胞性白血病(AML)。深入了解导致 AML 发生和发展的表观遗传修饰失调的机制对于设计有效的治疗方法可能至关重要。

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