Shaping Striated Muscles with Ubiquitin Proteasome System in Health and Disease

被引:15
|
作者
Hnia, Karim [1 ]
Clausen, Tim [2 ,3 ]
Moog-Lutz, Christel [4 ]
机构
[1] Univ Toulouse III, I2MC, INSERM, UMR1048, Toulouse, France
[2] Vienna BioCtr VBC, Res Inst Mol Pathol IMP, Campus Vienna Bioctr 1, A-1030 Vienna, Austria
[3] Med Univ Vienna, Vienna BioCtr VBC, A-1030 Vienna, Austria
[4] Univ Toulouse, IPBS, CNRS, UPS, Toulouse, France
关键词
RING FINGER 1; FUNCTIONAL INSUFFICIENCY; MULTIPLE-MYELOMA; LIGASE ACTIVITY; CARDIAC-MUSCLE; AUTOPHAGY; PROTEIN; ATROPHY; INHIBITOR; DEGRADATION;
D O I
10.1016/j.molmed.2019.05.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
For long-lived contractile cells, such as striated muscle cells, maintaining proteome integrity is a challenging task. These cells require hundreds of components that must be properly synthesized, folded, and incorporated into the basic contractile unit, the sarcomere. Muscle protein quality control in cells is mainly guaranteed by the ubiquitin-proteasome system (UPS), the lysosome-autophagy system, and various molecular chaperones. Recent studies establish the concept of dedicated UPS in the regulation of sarcomere assembly during development and in adult life to maintain the intricate and interwoven organization of protein complexes in muscle. Failure of sarcomere protein quality control often represents the basis of severe myopathies and cardiomyopathies in human, further highlighting its importance in producing and maintaining the contractile machinery of muscle cells in shape.
引用
收藏
页码:760 / 774
页数:15
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