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Research resource: RNA-Seq reveals unique features of the pancreatic β-cell transcriptome.研究资源:RNA测序揭示胰腺β细胞转录组的独特特征。
Mol Endocrinol. 2012 Oct;26(10):1783-92. doi: 10.1210/me.2012-1176. Epub 2012 Aug 21.
2
Androgen receptor-deficient islet β-cells exhibit alteration in genetic markers of insulin secretion and inflammation. A transcriptome analysis in the male mouse.雄激素受体缺陷的胰岛β细胞在胰岛素分泌和炎症的遗传标志物方面表现出改变。雄性小鼠的转录组分析。
J Diabetes Complications. 2017 May;31(5):787-795. doi: 10.1016/j.jdiacomp.2017.03.002. Epub 2017 Mar 9.
3
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Integrative transcriptome sequencing identifies trans-splicing events with important roles in human embryonic stem cell pluripotency.整合转录组测序鉴定出在人类胚胎干细胞多能性中具有重要作用的跨剪接事件。
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Diabetologia. 2018 Dec;61(12):2608-2620. doi: 10.1007/s00125-018-4735-7. Epub 2018 Oct 3.
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The transcriptional landscape of mouse beta cells compared to human beta cells reveals notable species differences in long non-coding RNA and protein-coding gene expression.与人类β细胞相比,小鼠β细胞的转录图谱揭示了长链非编码RNA和蛋白质编码基因表达方面显著的物种差异。
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Identification of islet-enriched long non-coding RNAs contributing to β-cell failure in type 2 diabetes.鉴定与 2 型糖尿病β细胞衰竭相关的胰岛富集长非编码 RNA。
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Cell Physiol Biochem. 2018;45(5):2031-2043. doi: 10.1159/000487983. Epub 2018 Mar 6.

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The Kv2.2 channel mediates the inhibition of prostaglandin E2 on glucose-stimulated insulin secretion in pancreatic β-cells.Kv2.2通道介导前列腺素E2对胰腺β细胞中葡萄糖刺激的胰岛素分泌的抑制作用。
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Emerging Roles of ncRNAs in Type 2 Diabetes Mellitus: From Mechanisms to Drug Discovery.非编码 RNA 在 2 型糖尿病中的新兴作用:从机制到药物发现。
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Commun Biol. 2024 Jan 16;7(1):104. doi: 10.1038/s42003-024-05783-9.
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The Association between the Differential Expression of lncRNA and Type 2 Diabetes Mellitus in People with Hypertriglyceridemia.长链非编码 RNA 的差异表达与伴有高甘油三酯血症的 2 型糖尿病之间的关系。
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Pharmacological blockade of the EP3 prostaglandin E receptor in the setting of type 2 diabetes enhances β-cell proliferation and identity and relieves oxidative damage.在 2 型糖尿病的背景下,药理学阻断 EP3 前列腺素 E 受体可增强β细胞的增殖和特性,并减轻氧化损伤。
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本文引用的文献

1
Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks.RNA-seq 实验中使用 TopHat 和 Cufflinks 的差异基因和转录本表达分析。
Nat Protoc. 2012 Mar 1;7(3):562-78. doi: 10.1038/nprot.2012.016.
2
Conserved function of lincRNAs in vertebrate embryonic development despite rapid sequence evolution.脊椎动物胚胎发育中 lincRNAs 的保守功能,尽管序列进化迅速。
Cell. 2011 Dec 23;147(7):1537-50. doi: 10.1016/j.cell.2011.11.055.
3
Targeted RNA sequencing reveals the deep complexity of the human transcriptome.靶向 RNA 测序揭示了人类转录组的深度复杂性。
Nat Biotechnol. 2011 Nov 13;30(1):99-104. doi: 10.1038/nbt.2024.
4
Clusters of conserved beta cell marker genes for assessment of beta cell phenotype.用于评估β细胞表型的簇状保守β细胞标记基因。
PLoS One. 2011;6(9):e24134. doi: 10.1371/journal.pone.0024134. Epub 2011 Sep 2.
5
Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses.整合注释人类大型长非编码 RNA 揭示了其全局特征和特定亚类。
Genes Dev. 2011 Sep 15;25(18):1915-27. doi: 10.1101/gad.17446611. Epub 2011 Sep 2.
6
Transcriptomes of the major human pancreatic cell types.人类主要胰腺细胞类型的转录组。
Diabetologia. 2011 Nov;54(11):2832-44. doi: 10.1007/s00125-011-2283-5. Epub 2011 Sep 1.
7
PhyloCSF: a comparative genomics method to distinguish protein coding and non-coding regions.PhyloCSF:一种用于区分蛋白质编码区和非编码区的比较基因组学方法。
Bioinformatics. 2011 Jul 1;27(13):i275-82. doi: 10.1093/bioinformatics/btr209.
8
Long noncoding RNAs and human disease.长非编码 RNA 与人类疾病。
Trends Cell Biol. 2011 Jun;21(6):354-61. doi: 10.1016/j.tcb.2011.04.001. Epub 2011 May 6.
9
RNA-sequence analysis of human B-cells.人类 B 细胞的 RNA 测序分析。
Genome Res. 2011 Jun;21(6):991-8. doi: 10.1101/gr.116335.110. Epub 2011 May 2.
10
Integrative genomics viewer.整合基因组浏览器。
Nat Biotechnol. 2011 Jan;29(1):24-6. doi: 10.1038/nbt.1754.

研究资源:RNA测序揭示胰腺β细胞转录组的独特特征。

Research resource: RNA-Seq reveals unique features of the pancreatic β-cell transcriptome.

作者信息

Ku Gregory M, Kim Hail, Vaughn Ian W, Hangauer Matthew J, Myung Oh Chang, German Michael S, McManus Michael T

机构信息

513 Parnassus Avenue, Box 0534, San Francisco, California 94143-0534, USA.

出版信息

Mol Endocrinol. 2012 Oct;26(10):1783-92. doi: 10.1210/me.2012-1176. Epub 2012 Aug 21.

DOI:10.1210/me.2012-1176
PMID:22915829
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3458219/
Abstract

The pancreatic β-cell is critical for the maintenance of glycemic control. Knowing the compendium of genes expressed in β-cells will further our understanding of this critical cell type and may allow the identification of future antidiabetes drug targets. Here, we report the use of next-generation sequencing to obtain nearly 1 billion reads from the polyadenylated RNA of islets and purified β-cells from mice. These data reveal novel examples of β-cell-specific splicing events, promoter usage, and over 1000 long intergenic noncoding RNA expressed in mouse β-cells. Many of these long intergenic noncoding RNA are β-cell specific, and we hypothesize that this large set of novel RNA may play important roles in β-cell function. Our data demonstrate unique features of the β-cell transcriptome.

摘要

胰腺β细胞对于维持血糖控制至关重要。了解β细胞中表达的基因全集将加深我们对这种关键细胞类型的理解,并可能有助于识别未来的抗糖尿病药物靶点。在此,我们报告使用下一代测序技术从小鼠胰岛和纯化的β细胞的聚腺苷酸化RNA中获得了近10亿条读数。这些数据揭示了β细胞特异性剪接事件、启动子使用的新例子,以及在小鼠β细胞中表达的1000多种长链基因间非编码RNA。这些长链基因间非编码RNA中的许多都是β细胞特异性的,我们推测这一大组新的RNA可能在β细胞功能中发挥重要作用。我们的数据证明了β细胞转录组的独特特征。