Arginylation Regulates Cytoskeleton Organization and Cell Division and Affects Mitochondria in Fission Yeast

被引:2
作者
Chen, Li [1 ]
Kashina, Anna [1 ]
机构
[1] Univ Penn, Sch Vet Med, Dept Biomed Sci, Philadelphia, PA 19104 USA
关键词
actin; arginylation; cytoskeleton; fission yeast; mitosis; RNA-PROTEIN TRANSFERASE; END RULE PATHWAY; POSTTRANSLATIONAL ARGINYLATION; ACTIN CYTOSKELETON; CDC42; IDENTIFICATION; CYTOKINESIS; DYNAMICS; POLARITY; GROWTH;
D O I
10.1128/mcb.00261-22
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
Protein arginylation mediated by arginyltransferase Ate1 is a posttranslational modification of emerging importance implicated in the regulation of mammalian embryogenesis, the cardiovascular system, tissue morphogenesis, cell migration, neurodegeneration, cancer, and aging. Ate1 deletion results in embryonic lethality in mice but does not affect yeast viability, making yeast an ideal system to study the molecular pathways regulated by arginylation. Here, we conducted a global analysis of cytoskeleton-related arginylation-dependent phenotypes in Schizosaccharomyces pombe, a fission yeast species that shares many fundamental features of higher eukaryotic cells. Our studies revealed roles of Ate1 in cell division, cell polarization, organelle transport, and interphase cytoskeleton organization and dynamics. We also found a role of Ate1 in mitochondria morphology and maintenance. Furthermore, targeted mass spectrometry analysis of the total Sc. pombe arginylome identified a number of arginylated proteins, including those that play direct roles in these processes; lack of their arginylation may be responsible for ate1-knockout phenotypes. Our work outlines global biological processes potentially regulated by arginylation and paves the way to unraveling the functions of protein arginylation that are conserved at multiple levels of evolution and potentially constitute the primary role of this modification in vivo. Protein arginylation mediated by arginyltransferase Ate1 is a posttranslational modification of emerging importance implicated in the regulation of mammalian embryogenesis, the cardiovascular system, tissue morphogenesis, cell migration, neurodegeneration, cancer, and aging. Ate1 deletion results in embryonic lethality in mice but does not affect yeast viability, making yeast an ideal system to study the molecular pathways regulated by arginylation. Here, we conducted a global analysis of cytoskeleton-related arginylation-dependent phenotypes in Schizosaccharomyces pombe, a fission yeast species that shares many fundamental features of higher eukaryotic cells.
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页数:14
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共 53 条
[1]  
Arai R, 2002, J CELL SCI, V115, P887
[2]  
BALZI E, 1990, J BIOL CHEM, V265, P7464
[3]   Cell Polarity in Yeast [J].
Chiou, Jian-geng ;
Balasubramanian, Mohan K. ;
Lew, Daniel J. .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 33, 2017, 33 :77-101
[4]   Arginylation of Myosin Heavy Chain Regulates Skeletal Muscle Strength [J].
Comachione, Anabelle S. ;
Leite, Felipe S. ;
Wang, Junling ;
Leu, Nicolae A. ;
Kalganov, Albert ;
Volgin, Denys ;
Han, Xuemei ;
Xu, Tao ;
Cheng, Yu-Shu ;
Yates, John R. R., III ;
Rassier, Dilson E. ;
Kashina, Anna .
CELL REPORTS, 2014, 8 (02) :469-475
[5]   Heat stress induced arginylation of HuR promotes alternative polyadenylation ofHsp70.3by regulating HuR stability and RNA binding [J].
Deka, Kamalakshi ;
Saha, Sougata .
CELL DEATH AND DIFFERENTIATION, 2021, 28 (02) :730-747
[6]   Protein arginylation regulates cellular stress response by stabilizing HSP70 and HSP40 transcripts [J].
Deka, Kamalakshi ;
Singh, Archana ;
Chakraborty, Surajit ;
Mukhopadhyay, Rupak ;
Saha, Sougata .
CELL DEATH DISCOVERY, 2016, 2
[7]   Conservation and specialization: The role of the exocyst in neuronal exocytosis [J].
EauClaire, S ;
Guo, W .
NEURON, 2003, 37 (03) :369-370
[8]  
Estravis Miguel, 2012, Commun Integr Biol, V5, P370, DOI 10.4161/cib.19977
[9]   Cdc42 - the centre of polarity [J].
Etienne-Manneville, S .
JOURNAL OF CELL SCIENCE, 2004, 117 (08) :1291-1300
[10]   Atg43 tethers isolation membranes to mitochondria to promote starvation-induced mitophagy in fission yeast [J].
Fukuda, Tomoyuki ;
Ebi, Yuki ;
Saigusa, Tetsu ;
Furukawa, Kentaro ;
Yamashita, Shun-ichi ;
Inoue, Keiichi ;
Kobayashi, Daiki ;
Yoshida, Yutaka ;
Kanki, Tomotake .
ELIFE, 2020, 9 :1-29