Residential College | false |
Status | 已發表Published |
Human β cell transcriptome analysis uncovers lncRNAs that are tissue-specific, dynamically regulated, and abnormally expressed in type 2 diabetes | |
Moran I.17; Akerman I.17; Van De Bunt M.5; Xie R.15; Benazra M.13; Nammo T.17; Arnes L.11; Nakic N.17; Garcia-Hurtado J.17; Rodriguez-Segui S.17; Pasquali L.17; Sauty-Colace C.13; Beucher A.17; Scharfmann R.8; Van Arensbergen J.17; Johnson P.R.1; Berry A.9; Lee C.4; Harkins T.4; Gmyr V.12; Pattou F.12; Kerr-Conte J.12; Piemonti L.10; Berney T.3; Hanley N.9; Gloyn A.L.1; Sussel L.11; Langman L.16; Brayman K.L.16; Sander M.15; McCarthy M.I.5; Ravassard P.13; Ferrer J.17 | |
2012-10-03 | |
Source Publication | Cell Metabolism |
ISSN | 1550-4131 |
Volume | 16Issue:4Pages:435-448 |
Abstract | A significant portion of the genome is transcribed as long noncoding RNAs (lncRNAs), several of which are known to control gene expression. The repertoire and regulation of lncRNAs in disease-relevant tissues, however, has not been systematically explored. We report a comprehensive strand-specific transcriptome map of human pancreatic islets and β cells, and uncover >1100 intergenic and antisense islet-cell lncRNA genes. We find islet lncRNAs that are dynamically regulated and show that they are an integral component of the β cell differentiation and maturation program. We sequenced the mouse islet transcriptome and identify lncRNA orthologs that are regulated like their human counterparts. Depletion of HI-LNC25, a β cell-specific lncRNA, downregulated GLIS3 mRNA, thus exemplifying a gene regulatory function of islet lncRNAs. Finally, selected islet lncRNAs were dysregulated in type 2 diabetes or mapped to genetic loci underlying diabetes susceptibility. These findings reveal a new class of islet-cell genes relevant to β cell programming and diabetes pathophysiology. © 2012 Elsevier Inc. |
DOI | 10.1016/j.cmet.2012.08.010 |
URL | View the original |
Indexed By | SCIE |
WOS Research Area | Cell Biology ; Endocrinology & Metabolism |
WOS Subject | Cell Biology ; Endocrinology & Metabolism |
WOS ID | WOS:000309948400007 |
Scopus ID | 2-s2.0-84867070330 |
Fulltext Access | |
Citation statistics | |
Document Type | Journal article |
Collection | Faculty of Health Sciences |
Affiliation | 1.Churchill Hospital 2.Research Institute 3.Cell Isolation and Transplantation Center 4.Life Technologies 5.Wellcome Trust Centre for Human Genetics 6.Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas 7.John Radcliffe Hospital 8.Universite Paris Descartes 9.University of Manchester 10.IRCCS San Raffaele Scientific Institute 11.Columbia University in the City of New York 12.University of Lille 13.Sorbonne Universite 14.Hospital Clinic Barcelona 15.University of California, San Diego 16.University of Virginia Medical School 17.Institut d'Investigacions Biomèdiques August Pi i Sunyer - IDIBAPS |
Recommended Citation GB/T 7714 | Moran I.,Akerman I.,Van De Bunt M.,et al. Human β cell transcriptome analysis uncovers lncRNAs that are tissue-specific, dynamically regulated, and abnormally expressed in type 2 diabetes[J]. Cell Metabolism, 2012, 16(4), 435-448. |
APA | Moran I.., Akerman I.., Van De Bunt M.., Xie R.., Benazra M.., Nammo T.., Arnes L.., Nakic N.., Garcia-Hurtado J.., Rodriguez-Segui S.., Pasquali L.., Sauty-Colace C.., Beucher A.., Scharfmann R.., Van Arensbergen J.., Johnson P.R.., Berry A.., Lee C.., Harkins T.., ...& Ferrer J. (2012). Human β cell transcriptome analysis uncovers lncRNAs that are tissue-specific, dynamically regulated, and abnormally expressed in type 2 diabetes. Cell Metabolism, 16(4), 435-448. |
MLA | Moran I.,et al."Human β cell transcriptome analysis uncovers lncRNAs that are tissue-specific, dynamically regulated, and abnormally expressed in type 2 diabetes".Cell Metabolism 16.4(2012):435-448. |
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