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本文引用的文献

1
Mouse-human experimental epigenetic analysis unmasks dietary targets and genetic liability for diabetic phenotypes.小鼠-人类实验性表观遗传学分析揭示糖尿病表型的饮食靶点和遗传易感性。
Cell Metab. 2015 Jan 6;21(1):138-49. doi: 10.1016/j.cmet.2014.12.014.
2
The Polycomb protein, Bmi1, regulates insulin sensitivity.多梳蛋白 Bmi1 调节胰岛素敏感性。
Mol Metab. 2014 Aug 27;3(8):794-802. doi: 10.1016/j.molmet.2014.08.002. eCollection 2014 Nov.
3
Genome-wide associations between genetic and epigenetic variation influence mRNA expression and insulin secretion in human pancreatic islets.基因与表观遗传变异之间的全基因组关联影响人类胰岛中的mRNA表达和胰岛素分泌。
PLoS Genet. 2014 Nov 6;10(11):e1004735. doi: 10.1371/journal.pgen.1004735. eCollection 2014 Nov.
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The role of epigenetic mechanisms in Notch signaling during development.表观遗传机制在发育过程中 Notch 信号转导中的作用。
J Cell Physiol. 2015 May;230(5):969-81. doi: 10.1002/jcp.24851.
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Generation of functional human pancreatic β cells in vitro.体外生成功能性人胰腺β细胞。
Cell. 2014 Oct 9;159(2):428-39. doi: 10.1016/j.cell.2014.09.040.
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Control of cell identity genes occurs in insulated neighborhoods in mammalian chromosomes.细胞身份基因的调控发生在哺乳动物染色体的绝缘区域。
Cell. 2014 Oct 9;159(2):374-387. doi: 10.1016/j.cell.2014.09.030.
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Dynamic GATA4 enhancers shape the chromatin landscape central to heart development and disease.动态GATA4增强子塑造了心脏发育和疾病核心的染色质景观。
Nat Commun. 2014 Sep 24;5:4907. doi: 10.1038/ncomms5907.
8
Diabetes recovery by age-dependent conversion of pancreatic δ-cells into insulin producers.通过胰腺δ细胞随年龄依赖性转化为胰岛素产生细胞实现糖尿病恢复。
Nature. 2014 Oct 23;514(7523):503-7. doi: 10.1038/nature13633. Epub 2014 Aug 20.
9
"RAS"ling β cells to proliferate for diabetes: why do we need MEN?“RAS”促使β细胞增殖以应对糖尿病:我们为何需要MEN?
J Clin Invest. 2014 Sep;124(9):3698-700. doi: 10.1172/JCI77764. Epub 2014 Aug 18.
10
Dynamics of genomic H3K27me3 domains and role of EZH2 during pancreatic endocrine specification.胰腺内分泌细胞特化过程中基因组H3K27me3结构域的动态变化及EZH2的作用
EMBO J. 2014 Oct 1;33(19):2157-70. doi: 10.15252/embj.201488671. Epub 2014 Aug 8.

表观遗传修饰和长链非编码RNA影响胰腺的发育和功能。

Epigenetic modifications and long noncoding RNAs influence pancreas development and function.

作者信息

Arnes Luis, Sussel Lori

机构信息

Department of Genetics and Development, Columbia University, New York, NY, USA.

Department of Genetics and Development, Columbia University, New York, NY, USA.

出版信息

Trends Genet. 2015 Jun;31(6):290-9. doi: 10.1016/j.tig.2015.02.008. Epub 2015 Mar 23.

DOI:10.1016/j.tig.2015.02.008
PMID:25812926
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4458180/
Abstract

Insulin-producing β cells within the pancreatic islet of Langerhans are responsible for maintaining glucose homeostasis; the loss or malfunction of β cells results in diabetes mellitus. Recent advances in cell purification strategies and sequencing technologies as well as novel molecular tools have revealed that epigenetic modifications and long noncoding RNAs (lncRNAs) represent an integral part of the transcriptional mechanisms regulating pancreas development and β cell function. Importantly, these findings have uncovered a new layer of gene regulation in the pancreas that can be exploited to enhance the restoration and/or repair of β cells to treat diabetes.

摘要

胰腺胰岛中产生胰岛素的β细胞负责维持葡萄糖稳态;β细胞的丧失或功能异常会导致糖尿病。细胞纯化策略和测序技术以及新型分子工具的最新进展表明,表观遗传修饰和长链非编码RNA(lncRNA)是调节胰腺发育和β细胞功能的转录机制的一个组成部分。重要的是,这些发现揭示了胰腺中基因调控的一个新层面,可用于增强β细胞的恢复和/或修复以治疗糖尿病。