骨髓细胞发育过程中细胞和巨细胞病毒基因的表观遗传调控。

Xue-Feng Liu, Mary Hummel, Michael Abecassis
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引用次数: 2

摘要

髓样细胞是携带巨细胞病毒的重要细胞类型。潜伏病毒DNA存在于CD34+祖细胞及其衍生的单核细胞中。然而,潜伏感染的单核细胞分化为成熟的巨噬细胞或树突状细胞会引起潜伏病毒的再激活。在造血发育过程中,多能性基因被抑制,谱系特异性基因被逐步激活。这个过程是由细胞类型特定的染色质状态控制的。造血系统中的增强子是高度动态的,由先锋(第一层)转录因子(TF)建立,它为第二和第三层TF结合奠定了基础。在这篇综述中,我们研究了调节髓细胞发育、细胞身份和激活的表观遗传机制,特别关注了调节髓细胞中病毒基因表达和病毒感染状态的因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Epigenetic regulation of cellular and cytomegalovirus genes during myeloid cell development.

Myeloid cells are important cell types that carry human cytomegalovirus. Latent viral DNA is present in CD34+ progenitor cells and their derived monocytes. However, differentiation of latently infected monocytes to mature macrophages or dendritic cells causes reactivation of latent viruses. During hematopoietic development, pluripotent genes are repressed, and lineage specific genes are activated in a step-wise manner. This process is governed by cell-type specific chromatin states. Enhancers in the hematopoietic system are highly dynamic and established by pioneer (first tier) transcription factors (TFs), which set the stage for second and third tier TF binding. In this review, we examine the epigenetic mechanisms that regulate myeloid cell development, cell identity, and activation with a special focus on factors that regulate viral gene expression and the status of viral infection in myeloid cells.

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