Illuminating the impact of N-terminal acetylation: from protein to physiology

被引:1
作者
Mctiernan, Nina [1 ]
Kjosas, Ine [1 ]
Arnesen, Thomas [1 ,2 ]
机构
[1] Univ Bergen, Dept Biomed, Bergen, Norway
[2] Haukeland Hosp, Dept Surg, Bergen, Norway
基金
欧洲研究理事会;
关键词
ARF-LIKE GTPASE; MUSCLE ALPHA-TROPOMYOSIN; END RULE PATHWAY; MOLECULAR-BASIS; SIR3; STABILIZES; ACETYLTRANSFERASE; YEAST; ACTIN; IDENTIFICATION; NATA;
D O I
10.1038/s41467-025-55960-5
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
07 ; 0710 ; 09 ;
摘要
N-terminal acetylation is a highly abundant protein modification in eukaryotic cells. This modification is catalysed by N-terminal acetyltransferases acting co- or post-translationally. Here, we review the eukaryotic N-terminal acetylation machinery: the enzymes involved and their substrate specificities. We also provide an overview of the impact of N-terminal acetylation, including its effects on protein folding, subcellular targeting, protein complex formation, and protein turnover. In particular, there may be competition between N-terminal acetyltransferases and other enzymes in defining protein fate. At the organismal level, N-terminal acetylation is highly influential, and its impairment was recently linked to cardiac dysfunction and neurodegenerative diseases.
引用
收藏
页数:15
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