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本文引用的文献

1
Pancreatic microexons regulate islet function and glucose homeostasis.胰腺微小外显子调节胰岛功能和葡萄糖稳态。
Nat Metab. 2023 Feb;5(2):219-236. doi: 10.1038/s42255-022-00734-2. Epub 2023 Feb 9.
2
Therapeutic Modulation of RNA Splicing in Malignant and Non-Malignant Disease.治疗性调控 RNA 剪接在恶性和非恶性疾病中的作用。
Trends Mol Med. 2021 Jul;27(7):643-659. doi: 10.1016/j.molmed.2021.04.005. Epub 2021 May 13.
3
A novel protein domain in an ancestral splicing factor drove the evolution of neural microexons.一个古老剪接因子中的新蛋白结构域驱动了神经微外显子的演化。
Nat Ecol Evol. 2019 Apr;3(4):691-701. doi: 10.1038/s41559-019-0813-6. Epub 2019 Mar 4.
4
An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms.可变剪接图谱和功能关联图集揭示了新的调控程序和基因,它们可同时表达多个主要的异构体。
Genome Res. 2017 Oct;27(10):1759-1768. doi: 10.1101/gr.220962.117. Epub 2017 Aug 30.
5
A highly conserved program of neuronal microexons is misregulated in autistic brains.在自闭症大脑中,一个高度保守的神经元微小外显子程序受到了失调调控。
Cell. 2014 Dec 18;159(7):1511-23. doi: 10.1016/j.cell.2014.11.035.
6
Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants.富含 2 型糖尿病风险相关变异的胰岛增强子簇。
Nat Genet. 2014 Feb;46(2):136-143. doi: 10.1038/ng.2870. Epub 2014 Jan 12.
7
Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing.通过高通量测序对人类转录组中可变剪接复杂性进行深度研究。
Nat Genet. 2008 Dec;40(12):1413-5. doi: 10.1038/ng.259. Epub 2008 Nov 2.
8
Gene structure prediction and alternative splicing analysis using genomically aligned ESTs.利用基因组比对的ESTs进行基因结构预测和可变剪接分析。
Genome Res. 2001 May;11(5):889-900. doi: 10.1101/gr.155001.
9
Initial sequencing and analysis of the human genome.人类基因组的初步测序与分析。
Nature. 2001 Feb 15;409(6822):860-921. doi: 10.1038/35057062.
10
Proteomics: new perspectives, new biomedical opportunities.蛋白质组学:新视角,新生物医学机遇。
Lancet. 2000 Nov 18;356(9243):1749-56. doi: 10.1016/S0140-6736(00)03214-1.

小巧而强大:葡萄糖稳态中的微外显子。

Small but mighty: microexons in glucose homeostasis.

机构信息

Department of Genetics, Stanford School of Medicine, Stanford, CA, USA.

Department of Genetics, Stanford School of Medicine, Stanford, CA, USA; Department of Pediatrics, Division of Endocrinology, Stanford School of Medicine, Stanford, CA, USA; Stanford Diabetes Research Center, Stanford School of Medicine, Stanford, CA, USA.

出版信息

Trends Genet. 2023 Jul;39(7):526-527. doi: 10.1016/j.tig.2023.04.003. Epub 2023 Apr 18.

DOI:10.1016/j.tig.2023.04.003
PMID:37080883
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11523908/
Abstract

Many molecular mechanisms underlying blood glucose homeostasis remain elusive. Juan-Mateu et al. find that pancreatic islet cells utilize a regulatory program, originally identified in neurons, that involves alternative splicing of microexons in genes important for insulin secretion or diabetes risk.

摘要

许多血糖稳态的分子机制仍然难以捉摸。Juan-Mateu 等人发现,胰岛细胞利用了一种最初在神经元中发现的调节程序,该程序涉及对胰岛素分泌或糖尿病风险相关基因的微外显子的选择性剪接。