T2DB: A Web Database for Long Non-Coding RNA Genes in Type II Diabetes.

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Rebecca Distefano, Mirolyuba Ilieva, Jens Hedelund Madsen, Hideshi Ishii, Masanori Aikawa, Sarah Rennie, Shizuka Uchida
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Abstract

Type II diabetes (T2D) is a growing health problem worldwide due to increased levels of obesity and can lead to other life-threatening diseases, such as cardiovascular and kidney diseases. As the number of individuals diagnosed with T2D rises, there is an urgent need to understand the pathogenesis of the disease in order to prevent further harm to the body caused by elevated blood glucose levels. Recent advances in long non-coding RNA (lncRNA) research may provide insights into the pathogenesis of T2D. Although lncRNAs can be readily detected in RNA sequencing (RNA-seq) data, most published datasets of T2D patients compared to healthy donors focus only on protein-coding genes, leaving lncRNAs to be undiscovered and understudied. To address this knowledge gap, we performed a secondary analysis of published RNA-seq data of T2D patients and of patients with related health complications to systematically analyze the expression changes of lncRNA genes in relation to the protein-coding genes. Since immune cells play important roles in T2D, we conducted loss-of-function experiments to provide functional data on the T2D-related lncRNA USP30-AS1, using an in vitro model of pro-inflammatory macrophage activation. To facilitate lncRNA research in T2D, we developed a web application, T2DB, to provide a one-stop-shop for expression profiling of protein-coding and lncRNA genes in T2D patients compared to healthy donors or subjects without T2D.

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T2DB:II型糖尿病中长非编码RNA基因的网络数据库。
由于肥胖水平的增加,II型糖尿病(T2D)在全球范围内是一个日益严重的健康问题,并可能导致其他危及生命的疾病,如心血管和肾脏疾病。随着被诊断为T2D的人数增加,迫切需要了解该疾病的发病机制,以防止血糖水平升高对身体造成进一步伤害。长期非编码RNA(lncRNA)研究的最新进展可能为T2D的发病机制提供见解。尽管lncRNA可以很容易地在RNA测序(RNA-seq)数据中检测到,但与健康供体相比,大多数已发表的T2D患者数据集只关注蛋白质编码基因,这使得lncRNA尚未被发现和研究不足。为了解决这一知识差距,我们对T2D患者和有相关健康并发症的患者的已发表RNA-seq数据进行了二次分析,以系统分析lncRNA基因与蛋白质编码基因的表达变化。由于免疫细胞在T2D中发挥重要作用,我们使用促炎巨噬细胞激活的体外模型进行了功能丧失实验,以提供T2D相关lncRNA USP30-AS1的功能数据。为了促进T2D中lncRNA的研究,我们开发了一个名为T2DB的网络应用程序,与健康供体或无T2D的受试者相比,为T2D患者的蛋白质编码和lncRNA基因的表达谱分析提供了一站式服务。
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来源期刊
Non-Coding RNA
Non-Coding RNA Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
6.70
自引率
4.70%
发文量
74
审稿时长
10 weeks
期刊介绍: Functional studies dealing with identification, structure-function relationships or biological activity of: small regulatory RNAs (miRNAs, siRNAs and piRNAs) associated with the RNA interference pathway small nuclear RNAs, small nucleolar and tRNAs derived small RNAs other types of small RNAs, such as those associated with splice junctions and transcription start sites long non-coding RNAs, including antisense RNAs, long ''intergenic'' RNAs, intronic RNAs and ''enhancer'' RNAs other classes of RNAs such as vault RNAs, scaRNAs, circular RNAs, 7SL RNAs, telomeric and centromeric RNAs regulatory functions of mRNAs and UTR-derived RNAs catalytic and allosteric (riboswitch) RNAs viral, transposon and repeat-derived RNAs bacterial regulatory RNAs, including CRISPR RNAS Analysis of RNA processing, RNA binding proteins, RNA signaling and RNA interaction pathways: DICER AGO, PIWI and PIWI-like proteins other classes of RNA binding and RNA transport proteins RNA interactions with chromatin-modifying complexes RNA interactions with DNA and other RNAs the role of RNA in the formation and function of specialized subnuclear organelles and other aspects of cell biology intercellular and intergenerational RNA signaling RNA processing structure-function relationships in RNA complexes RNA analyses, informatics, tools and technologies: transcriptomic analyses and technologies development of tools and technologies for RNA biology and therapeutics Translational studies involving long and short non-coding RNAs: identification of biomarkers development of new therapies involving microRNAs and other ncRNAs clinical studies involving microRNAs and other ncRNAs.
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