Identification of novel mRNAs and lncRNAs associated with mouse experimental colitis and human inflammatory bowel disease

被引:13
作者
Rankin, Carl Robert [1 ]
Theodorou, Evangelos [2 ]
Law, Ivy Ka Man [1 ]
Rowe, Lorraine [1 ]
Kokkotou, Efi [2 ]
Pekow, Joel [3 ]
Wang, Jiafang [4 ]
Martin, Martin G. [4 ]
Pothoulakis, Charalabos [1 ]
Padua, David [1 ,5 ]
机构
[1] Univ Calif Los Angeles, Dept Med, David Geffen Sch Med, Div Digest Dis, Los Angeles, CA 90073 USA
[2] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Div Gastroenterol, Boston, MA USA
[3] Univ Chicago, Div Gastroenterol, Chicago, IL 60637 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Pediat, Los Angeles, CA 90073 USA
[5] Vet Affairs Greater Los Angeles Healthcare Syst, Div Gastroenterol Hepatol & Parenteral Nutr, Los Angeles, CA 90073 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2018年 / 315卷 / 05期
关键词
inflammatory bowel disease; long noncoding RNA; RNA-seq; ulcerative colitis; LONG NONCODING RNA; ULCERATIVE-COLITIS; DIFFERENTIAL EXPRESSION; GENE-EXPRESSION; MODIFIER FAT10; SEQ; VALIDATION; ACTIVATION; SUPPRESSOR; PATTERNS;
D O I
10.1152/ajpgi.00077.2018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Inflammatory bowel disease (IBD) is a complex disorder that is associated with significant morbidity. While many recent advances have been made with new diagnostic and therapeutic tools, a deeper understanding of its basic pathophysiology is needed to continue this trend toward improving treatments. By utilizing an unbiased, high-throughput transcriptomic analysis of two well-established mouse models of colitis, we set out to uncover novel coding and noncoding RNAs that are differentially expressed in the setting of colonic inflammation. RNA-seq analysis was performed using colonic tissue from two mouse models of colitis. a dextran sodium sulfate-induced model and a genetic-induced model in mice lacking IL-10. We identified 81 coding RNAs that were commonly altered in both experimental models. Of these coding RNAs. 12 of the human orthologs were differentially expressed in a transcriptomic analysis of IBD patients. Interestingly, 5 of the 12 of human differentially expressed genes have not been previously identified as IBD-associated genes, including ubiquitin D. Our analysis also identified 15 noncoding RNAs that were differentially expressed in either mouse model. Surprisingly, only three noncoding RNAs were commonly dysregulated in both of these models. The discovery of these new coding and noncoding RNAs expands our transcriptional knowledge of mouse models of IBD and offers additional targets to deepen our understanding of the pathophysiology of IBD. NEW & NOTEWORTHY Much of the genome is transcribed as non-protein-coding RNAs; however, their role in inflammatory bowel disease is largely unknown. This study represents the first of its kind to analyze the expression of long noncoding RNAs in two mouse models of inflammatory bowel disease and correlate them to human clinical samples. Using high-throughput RNA-sey analysis, we identified new coding and noncoding RNAs that were differentially expressed such as ubiquitin D and 5730437C11Rik.
引用
收藏
页码:G722 / G733
页数:12
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