N-degron通路:从基础科学到治疗应用

IF 2.6 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et Biophysica Acta-Gene Regulatory Mechanisms Pub Date : 2023-06-01 DOI:10.1016/j.bbagrm.2023.194934
Ah Jung Heo , Su Bin Kim , Yong Tae Kwon , Chang Hoon Ji
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引用次数: 1

摘要

n -降解途径是一个降解系统,其中单个n端氨基酸(Nt)调节蛋白质和其他生物材料的半衰期。这些决定因子被称为n -degron,被n -识别蛋白识别,并将它们与泛素(Ub)-蛋白酶体系统(UPS)或自噬-溶酶体系统(ALS)联系起来。在UPS中,Arg/N-degron途径以t-精氨酸(Nt-Arg)和其他N-degron为靶点,通过UBR盒n识别蛋白组装Lys48 (K48)连接的Ub链,进行蛋白酶体蛋白水解。在ALS中,Arg/N-degrons被n -识别蛋白p62/SQSTSM-1/ sequestoome -1识别,诱导底物的顺式降解和各种载体(如蛋白质聚集体和亚细胞细胞器)的反式降解。UPS和ALP之间的串扰涉及到Ub代码的重编程。真核细胞发展出多种途径来针对所有20种主要氨基酸进行降解。在这里,我们讨论了N-degron通路的组成、调控和功能,重点介绍了Arg/N-degron和n - recognition的基本机制和治疗应用。
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The N-degron pathway: From basic science to therapeutic applications

The N-degron pathway is a degradative system in which single N-terminal (Nt) amino acids regulate the half-lives of proteins and other biological materials. These determinants, called N-degrons, are recognized by N-recognins that link them to the ubiquitin (Ub)-proteasome system (UPS) or autophagy-lysosome system (ALS). In the UPS, the Arg/N-degron pathway targets the Nt-arginine (Nt-Arg) and other N-degrons to assemble Lys48 (K48)-linked Ub chains by UBR box N-recognins for proteasomal proteolysis. In the ALS, Arg/N-degrons are recognized by the N-recognin p62/SQSTSM-1/Sequestosome-1 to induce cis-degradation of substrates and trans-degradation of various cargoes such as protein aggregates and subcellular organelles. This crosstalk between the UPS and ALP involves reprogramming of the Ub code. Eukaryotic cells developed diverse ways to target all 20 principal amino acids for degradation. Here we discuss the components, regulation, and functions of the N-degron pathways, with an emphasis on the basic mechanisms and therapeutic applications of Arg/N-degrons and N-recognins.

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来源期刊
CiteScore
9.20
自引率
2.10%
发文量
63
审稿时长
44 days
期刊介绍: BBA Gene Regulatory Mechanisms includes reports that describe novel insights into mechanisms of transcriptional, post-transcriptional and translational gene regulation. Special emphasis is placed on papers that identify epigenetic mechanisms of gene regulation, including chromatin, modification, and remodeling. This section also encompasses mechanistic studies of regulatory proteins and protein complexes; regulatory or mechanistic aspects of RNA processing; regulation of expression by small RNAs; genomic analysis of gene expression patterns; and modeling of gene regulatory pathways. Papers describing gene promoters, enhancers, silencers or other regulatory DNA regions must incorporate significant functions studies.
期刊最新文献
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