Sculpting nuclear envelope identity from the endoplasmic reticulum during the cell cycle

被引:10
作者
Deolal, Pallavi [1 ,2 ]
Scholz, Julia [1 ,2 ,3 ,4 ]
Ren, Kaike [1 ,2 ,3 ,4 ]
Bragulat-Teixidor, Helena [1 ,2 ,3 ,4 ]
Otsuka, Shotaro [1 ,2 ,5 ]
机构
[1] Max Perutz Labs, Vienna Bioctr Campus VBC, Vienna, Austria
[2] Med Univ Vienna, Ctr Med Biochem, Dept Mol Biol, Vienna, Austria
[3] Univ Vienna, Doctoral Sch, Vienna Bioctr PhD Program, Vienna, Austria
[4] Med Univ Vienna, Vienna, Austria
[5] Max Perutz Labs, Vienna Bioctr Campus VBC,Dr Bohr Gasse 9, A-1030 Vienna, Austria
关键词
Cell cycle; endoplasmic reticulum; ER-NE junction; mitosis; nuclear assembly; nuclear envelope; nuclear pore complex; TO-TUBULE TRANSFORMATION; PROTEIN-QUALITY CONTROL; MEMBRANE-PROTEINS; AUTOPHAGY DEGRADES; PORE COMPLEXES; SUN PROTEINS; E3; LIGASE; ER; RECRUITMENT; MECHANISMS;
D O I
10.1080/19491034.2023.2299632
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The nuclear envelope (NE) regulates nuclear functions, including transcription, nucleocytoplasmic transport, and protein quality control. While the outer membrane of the NE is directly continuous with the endoplasmic reticulum (ER), the NE has an overall distinct protein composition from the ER, which is crucial for its functions. During open mitosis in higher eukaryotes, the NE disassembles during mitotic entry and then reforms as a functional territory at the end of mitosis to reestablish nucleocytoplasmic compartmentalization. In this review, we examine the known mechanisms by which the functional NE reconstitutes from the mitotic ER in the continuous ER-NE endomembrane system during open mitosis. Furthermore, based on recent findings indicating that the NE possesses unique lipid metabolism and quality control mechanisms distinct from those of the ER, we explore the maintenance of NE identity and homeostasis during interphase. We also highlight the potential significance of membrane junctions between the ER and NE.
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页数:20
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