The Contribution of Transcriptional Coregulators in the Maintenance of β-cell Function and Identity.

Abstract:

:Islet 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.

journal_name

Endocrinology

journal_title

Endocrinology

authors

Davidson RK,Kanojia S,Spaeth JM

doi

10.1210/endocr/bqaa213

subject

Has Abstract

pub_date

2021-02-01 00:00:00

issue

2

eissn

0013-7227

issn

1945-7170

pii

5992209

journal_volume

162

pub_type

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