A Network of microRNAs Acts to Promote Cell Cycle Exit and Differentiation of Human Pancreatic Endocrine Cells
Year: 2019
Type: article
Abstract: Pancreatic endocrine cell differentiation is orchestrated by the action of transcription factors that operate in a gene regulatory network to activate endocrine lineage genes and repress lineage-inappropriate genes. MicroRNAs (miRNAs) are important modulators of gene expression, yet their role in endocrine cell differentiation has not been systematically explored. Here we characterize miRNA-regulatory networks active in human endocrine cell differentiation by combining small RNA sequencing, miRNA over-expression, and network modeling approaches. Our analysis identified Let-7g, Let-7a, miR-200a, miR-127, and miR-375 as endocrine-enriched miRNAs that drive endocrine cell differentiation-associated gene expression changes. These miRNAs are predicted to target different transcription factors, which converge on genes involved in cell cycle regulation. When expressed in human embryonic stem cell-derived pancreatic progenitors, these miRNAs induce cell cycle exit and promote endocrine cell differentiation. Our study delineates the role of miRNAs in human endocrine cell differentiation and identifies miRNAs that could facilitate endocrine cell reprogramming.
Source: iScience
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,000
Funders: California Institute for Regenerative Medicine, Larry L. Hillblom Foundation, Juvenile Diabetes Research Foundation United Kingdom, Juvenile Diabetes Research Foundation United States of America, M.S.I. Foundation, National Institutes of Health, University of California, San Diego, National Cancer Institute, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: G1535915583, G2651376736, G2701041615, Deciphering transcriptional control of pancreatic beta-cell maturation in vitro, G5941497103, G598865872, G6331392353, Novel insights into nutrient-dependent regulation of beta cell proliferation, Epigenetic determinants of beta cell development and function, G9000106514, G9000140433, Cancer Biology, Informatics & Omics (CBIO) Training Program, Integrated Islet Distribution Program (U24) - 2021, Diabetes Research Center (DRC)
OpenAlex ID: W2985025435
