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线粒体与细胞间变异性的非遗传起源:多即不同。

Mitochondria and the non-genetic origins of cell-to-cell variability: More is different.

作者信息

Guantes Raúl, Díaz-Colunga Juan, Iborra Francisco J

机构信息

Department of Condensed Matter Physics, Materials Science Institute 'Nicolás Cabrera' and Institute of Condensed Matter Physics (IFIMAC), Universidad Autónoma de Madrid, Campus de Cantoblanco, Madrid, Spain.

Centro Nacional de Biotecnología, CSIC, Campus de Cantoblanco, Madrid, Spain.

出版信息

Bioessays. 2016 Jan;38(1):64-76. doi: 10.1002/bies.201500082. Epub 2015 Dec 12.

Abstract

Gene expression activity is heterogeneous in a population of isogenic cells. Identifying the molecular basis of this variability will improve our understanding of phenomena like tumor resistance to drugs, virus infection, or cell fate choice. The complexity of the molecular steps and machines involved in transcription and translation could introduce sources of randomness at many levels, but a common constraint to most of these processes is its energy dependence. In eukaryotic cells, most of this energy is provided by mitochondria. A clonal population of cells may show a large variability in the number and functionality of mitochondria. Here, we discuss how differences in the mitochondrial content of each cell contribute to heterogeneity in gene products. Changes in the amount of mitochondria can also entail drastic alterations of a cell's gene expression program, which ultimately leads to phenotypic diversity. Also watch the Video Abstract.

摘要

在同基因细胞群体中,基因表达活性是异质的。确定这种变异性的分子基础将增进我们对诸如肿瘤耐药性、病毒感染或细胞命运选择等现象的理解。转录和翻译过程中涉及的分子步骤和机制的复杂性可能在多个层面引入随机性来源,但这些过程大多共同面临的一个限制是其能量依赖性。在真核细胞中,大部分能量由线粒体提供。一群克隆细胞可能在线粒体的数量和功能上表现出很大的变异性。在这里,我们讨论每个细胞中线粒体含量的差异如何导致基因产物的异质性。线粒体数量的变化也可能导致细胞基因表达程序的剧烈改变,最终导致表型多样性。另请观看视频摘要。

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