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埃及狒狒中与ε-、γ-和β-珠蛋白基因启动子相关的染色质DNA甲基化和组蛋白共价修饰的发育变化。

Developmental changes in DNA methylation and covalent histone modifications of chromatin associated with the epsilon-, gamma-, and beta-globin gene promoters in Papio anubis.

作者信息

Lavelle Donald, Vaitkus Kestis, Hankewych Maria, Singh Mahipal, DeSimone Joseph

机构信息

Jesse Brown VA Medical Center and Department of Medicine, University of Illinois, MP151C, 820 S. Damen Ave., Chicago, IL 60612, USA.

出版信息

Blood Cells Mol Dis. 2006 Mar-Apr;36(2):269-78. doi: 10.1016/j.bcmd.2006.01.004. Epub 2006 Mar 9.

Abstract

The baboon is a suitable and relevant animal model to study the mechanism of human globin gene switching. This investigation addresses the role of DNA methylation and histone coding in globin gene switching in the baboon, Papio anubis. Bisulfite sequencing and chromatin immunoprecipitation studies were performed in erythroid cells purified from fetuses of varying gestational ages and from adult bone marrow to analyze the manner that changes in DNA methylation of the epsilon-, gamma-, and beta-globin promoters and association of ac-H3, ac-H4, H3-dimeK4, H3-dimeK36, and H3-dimeK79 with the epsilon-, gamma-, and beta-globin promoters occur during development. Changes in DNA methylation of the epsilon- and gamma-globin gene promoters during transitional stages of globin gene switching were consistent with the stochastic model of methylation and a role of DNA methylation in gene silencing. Enrichment of ac-H3, ac-H4, and pol II at the promoters of developmentally active genes was observed, while the pattern of distribution of H3-dimeK4 and H3-dimeK79 suggests that these modifications are found near both currently and formerly active promoters. Enrichment of H3-dimeK36 at the silenced epsilon-globin gene promoter was observed. These studies demonstrate that coordinated epigenetic modifications in the chromatin structure of the beta-like globin gene promoters accompany the highly regulated changes in expression patterns of these genes during development.

摘要

狒狒是研究人类珠蛋白基因转换机制的合适且相关的动物模型。本研究探讨了DNA甲基化和组蛋白编码在东非狒狒(Papio anubis)珠蛋白基因转换中的作用。对从不同胎龄胎儿和成年骨髓中纯化的红细胞进行了亚硫酸氢盐测序和染色质免疫沉淀研究,以分析在发育过程中,ε-、γ-和β-珠蛋白启动子的DNA甲基化变化以及ac-H3、ac-H4、H3-dimeK4、H3-dimeK36和H3-dimeK79与ε-、γ-和β-珠蛋白启动子的结合方式。在珠蛋白基因转换的过渡阶段,ε-和γ-珠蛋白基因启动子的DNA甲基化变化与甲基化的随机模型以及DNA甲基化在基因沉默中的作用一致。观察到发育活跃基因启动子处ac-H3、ac-H4和pol II的富集,而H3-dimeK4和H3-dimeK79的分布模式表明,这些修饰在当前和以前活跃的启动子附近均有发现。在沉默的ε-珠蛋白基因启动子处观察到H3-dimeK36的富集。这些研究表明,在发育过程中,β-样珠蛋白基因启动子染色质结构中的协同表观遗传修饰伴随着这些基因表达模式的高度调控变化。

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