| Literature DB >> 28245910 |
Nathan Lawlor1, Shubham Khetan2, Duygu Ucar3, Michael L Stitzel4.
Abstract
Pancreatic islet dysfunction and beta cell failure are hallmarks of type 2 diabetes mellitus (T2DM) pathogenesis. In this review, we discuss how genome-wide association studies (GWASs) and recent developments in islet (epi)genome and transcriptome profiling (particularly single cell analyses) are providing novel insights into the genetic, environmental, and cellular contributions to islet (dys)function and T2DM pathogenesis. Moving forward, study designs that interrogate and model genetic variation [e.g., allelic profiling and (epi)genome editing] will be critical to dissect the molecular genetics of T2DM pathogenesis, to build next-generation cellular and animal models, and to develop precision medicine approaches to detect, treat, and prevent islet (dys)function and T2DM.Entities:
Keywords: Type 2 diabetes (T2D); epigenomics; genomics; pancreatic islets; single cell; transcriptomics
Mesh:
Year: 2017 PMID: 28245910 PMCID: PMC5458785 DOI: 10.1016/j.tig.2017.01.010
Source DB: PubMed Journal: Trends Genet ISSN: 0168-9525 Impact factor: 11.639