Davidson, Rebecca K.Kanojia, SukratiSpaeth, Jason M.2023-03-302023-03-302021Davidson RK, Kanojia S, Spaeth JM. The Contribution of Transcriptional Coregulators in the Maintenance of β-cell Function and Identity. Endocrinology. 2021;162(2):bqaa213. doi:10.1210/endocr/bqaa213https://hdl.handle.net/1805/32140Islet β-cell dysfunction that leads to impaired insulin secretion is a principal source of pathology of diabetes. In type 2 diabetes, this breakdown in β-cell health is associated with compromised islet-enriched transcription factor (TF) activity that disrupts gene expression programs essential for cell function and identity. TF activity is modulated by recruited coregulators that govern activation and/or repression of target gene expression, thereby providing a supporting layer of control. To date, more than 350 coregulators have been discovered that coordinate nucleosome rearrangements, modify histones, and physically bridge general transcriptional machinery to recruited TFs; however, relatively few have been attributed to β-cell function. Here, we will describe recent findings on those coregulators with direct roles in maintaining islet β-cell health and identity and discuss how disruption of coregulator activity is associated with diabetes pathogenesis.en-USPublisher PolicyIsletβ-cell identityβ-cell functionTranscriptionCoregulatorThe Contribution of Transcriptional Coregulators in the Maintenance of β-cell Function and IdentityArticle