Proteome complexity and the forces that drive proteome imbalance

被引:198
作者
Harper, J. Wade [1 ]
Bennett, Eric J. [2 ]
机构
[1] Harvard Med Sch, Dept Cell Biol, Boston, MA 02115 USA
[2] Univ Calif San Diego, Sect Cell & Dev Biol, Div Biol Sci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
N-TERMINAL ACETYLATION; UBIQUITIN-PROTEASOME-SYSTEM; EMBRYONIC STEM-CELLS; QUALITY-CONTROL; COPY-NUMBER; AAA-ATPASE; COTRANSLATIONAL UBIQUITINATION; SACCHAROMYCES-CEREVISIAE; TRANSLATION INITIATION; RIBOSOME BIOGENESIS;
D O I
10.1038/nature19947
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The cellular proteome is a complex microcosm of structural and regulatory networks that requires continuous surveillance and modification to meet the dynamic needs of the cell. It is therefore crucial that the protein flux of the cell remains in balance to ensure proper cell function. Genetic alterations that range from chromosome imbalance to oncogene activation can affect the speed, fidelity and capacity of protein biogenesis and degradation systems, which often results in proteome imbalance. An improved understanding of the causes and consequences of proteome imbalance is helping to reveal how these systems can be targeted to treat diseases such as cancer.
引用
收藏
页码:328 / 338
页数:11
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