SUMOylation, a multifaceted regulatory mechanism in the pancreatic beta cells. (July 2020)
- Record Type:
- Journal Article
- Title:
- SUMOylation, a multifaceted regulatory mechanism in the pancreatic beta cells. (July 2020)
- Main Title:
- SUMOylation, a multifaceted regulatory mechanism in the pancreatic beta cells
- Authors:
- Li, Na
Zhang, Shu
Xiong, Fei
Eizirik, Decio L.
Wang, Cong-Yi - Abstract:
- Highlights: We summarize recent progress about how SUMOylation regulates beta cell function and viability. SUMOylation levels in beta cells are influenced by the cellular redox status. SUMOylation interplays with other PTMs (e.g., phosphorylation, ubiquitination and Neddylation) in beta cells SUMOylation can affect beta cell senescence probably by modifying senescence-related key molecules, such as NOTCH1 and p53. SUMOylation is a promising modulator in beta cell RNA processing. Abstract: SUMOylation is an evolutionarily conserved post-translational modification (PTM) that regulates protein subcellular localization, stability, conformation, transcription and enzymatic activity. Recent studies indicate that SUMOylation plays a key role in insulin gene expression, glucose metabolism and insulin exocytosis under physiological conditions in the pancreatic beta cells. Furthermore, SUMOylation is implicated in beta cell survival and recovery following exposure to oxidative stress, ER stress and inflammatory mediators under pathological situations. SUMOylation is closely regulated by the cellular redox status, and it collaborates with other PTMs such as phosphorylation, ubiquitination, and NEDDylation, to maintain beta cellular homeostasis. We hereby provide an update on recent findings regarding the role of SUMOylation in the regulation of pancreatic beta cell viability and function, and discuss its potential implication in beta cell senescence and RNA processing ( e.g ., pre-mRNAHighlights: We summarize recent progress about how SUMOylation regulates beta cell function and viability. SUMOylation levels in beta cells are influenced by the cellular redox status. SUMOylation interplays with other PTMs (e.g., phosphorylation, ubiquitination and Neddylation) in beta cells SUMOylation can affect beta cell senescence probably by modifying senescence-related key molecules, such as NOTCH1 and p53. SUMOylation is a promising modulator in beta cell RNA processing. Abstract: SUMOylation is an evolutionarily conserved post-translational modification (PTM) that regulates protein subcellular localization, stability, conformation, transcription and enzymatic activity. Recent studies indicate that SUMOylation plays a key role in insulin gene expression, glucose metabolism and insulin exocytosis under physiological conditions in the pancreatic beta cells. Furthermore, SUMOylation is implicated in beta cell survival and recovery following exposure to oxidative stress, ER stress and inflammatory mediators under pathological situations. SUMOylation is closely regulated by the cellular redox status, and it collaborates with other PTMs such as phosphorylation, ubiquitination, and NEDDylation, to maintain beta cellular homeostasis. We hereby provide an update on recent findings regarding the role of SUMOylation in the regulation of pancreatic beta cell viability and function, and discuss its potential implication in beta cell senescence and RNA processing ( e.g ., pre-mRNA splicing and mRNA methylation). Through which we intend to provide novel insights into this fundamental biological process regarding both maintenance of beta cell viability and functionality, and beta cell dysfunction in diabetes mellitus. … (more)
- Is Part Of:
- Seminars in cell & developmental biology. Volume 103(2020)
- Journal:
- Seminars in cell & developmental biology
- Issue:
- Volume 103(2020)
- Issue Display:
- Volume 103, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 103
- Issue:
- 2020
- Issue Sort Value:
- 2020-0103-2020-0000
- Page Start:
- 51
- Page End:
- 58
- Publication Date:
- 2020-07
- Subjects:
- T1D type 1 diabetes -- T2D type 2 diabetes -- PTM post-translational modification -- ROS reactive oxygen species -- STZ streptozotocin -- NEDD neural precursor cell-expressed developmentally downregulated -- PDSM phosphorylation dependent SUMOylation motif -- PML progressive multifocal leukoencephalopathy -- SASP senescence associated secretory phenotype -- GSIS glucose stimulated insulin secretion -- AD Alzheimer's disease -- ASC adipose derived stem cell -- Rb retinoblastoma protein -- CDK2 cyclin dependent kinase2 -- PKR protein kinase receptor -- TPR translocated promoter region -- MEF mouse embryonic fibroblast -- SENPs SUMO-specific proteases -- snRNP small nuclear ribonucleoprotein particle -- SRSF1 serine/arginine-rich splicing factor -- Prp3 pre-mRNA processing factor3 -- Mettl3/14 N6-adenosine-methyltrasferase like3/14 -- WTAP WT1 associated protein -- m6A N6-methyladenosine -- 5-mC 5-methylcytosine
SUMOylation -- Pancreatic beta cell -- Insulin -- Cell viability -- Diabetes mellitus
Cytology -- Periodicals
Developmental biology -- Periodicals
571.6 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10849521 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.semcdb.2020.03.008 ↗
- Languages:
- English
- ISSNs:
- 1084-9521
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8239.448346
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13557.xml