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核微环境支持细胞增殖和分化的转录调控机制的组装与组织。

Nuclear microenvironments support assembly and organization of the transcriptional regulatory machinery for cell proliferation and differentiation.

作者信息

Stein Gary S, Lian Jane B, van Wijnen Andre J, Stein Janet L, Javed Amjad, Montecino Martin, Zaidi S Kaleem, Young Daniel, Choi Je-Yong, Gutierrez Soraya, Pockwinse Shirwin

机构信息

Department of Cell Biology and Cancer Center, University of Massachusetts Medical School, 55 Lake Ave. N., Worcester, Massachusetts 01655, USA.

出版信息

J Cell Biochem. 2004 Feb 1;91(2):287-302. doi: 10.1002/jcb.10777.

Abstract

The temporal and spatial organization of transcriptional regulatory machinery provides microenvironments within the nucleus where threshold concentrations of genes and cognate factors facilitate functional interactions. Conventional biochemical, molecular, and in vivo genetic approaches, together with high throughput genomic and proteomic analysis are rapidly expanding our database of regulatory macromolecules and signaling pathways that are requisite for control of genes that govern proliferation and differentiation. There is accruing insight into the architectural organization of regulatory machinery for gene expression that suggests signatures for biological control. Localized scaffolding of regulatory macromolecules at strategic promoter sites and focal compartmentalization of genes, transcripts, and regulatory factors within intranuclear microenvironments provides an infrastructure for combinatorial control of transcription that is operative within the three dimensional context of nuclear architecture.

摘要

转录调控机制的时空组织在细胞核内提供了微环境,在这些微环境中,基因和相关因子的阈值浓度促进了功能相互作用。传统的生化、分子和体内遗传学方法,以及高通量基因组和蛋白质组分析,正在迅速扩展我们关于调控大分子和信号通路的数据库,这些对于控制支配增殖和分化的基因是必不可少的。我们对基因表达调控机制的结构组织有了越来越多的认识,这表明了生物控制的特征。调控大分子在战略启动子位点的局部支架作用以及基因、转录本和调控因子在核内微环境中的局部区域化,为转录的组合控制提供了一个基础设施,该基础设施在核结构的三维背景下起作用。

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