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本文引用的文献

1
The structures of nonprotein-coding RNAs that drive internal ribosome entry site function.驱动内部核糖体进入位点功能的非蛋白编码 RNA 结构。
Wiley Interdiscip Rev RNA. 2012 Mar-Apr;3(2):195-212. doi: 10.1002/wrna.1105. Epub 2012 Jan 3.
2
Short-chain fatty acids stimulate glucagon-like peptide-1 secretion via the G-protein-coupled receptor FFAR2.短链脂肪酸通过 G 蛋白偶联受体 FFAR2 刺激胰高血糖素样肽-1 的分泌。
Diabetes. 2012 Feb;61(2):364-71. doi: 10.2337/db11-1019. Epub 2011 Dec 21.
3
Short-chain fatty acids and ketones directly regulate sympathetic nervous system via G protein-coupled receptor 41 (GPR41).短链脂肪酸和酮体通过 G 蛋白偶联受体 41(GPR41)直接调节交感神经系统。
Proc Natl Acad Sci U S A. 2011 May 10;108(19):8030-5. doi: 10.1073/pnas.1016088108. Epub 2011 Apr 25.
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A protocol for islet isolation from mouse pancreas.从鼠胰腺中分离胰岛的方案。
Nat Protoc. 2009;4(11):1649-52. doi: 10.1038/nprot.2009.150. Epub 2009 Oct 22.
5
A rat brain bicistronic gene with an internal ribosome entry site codes for a phencyclidine-binding protein with cytotoxic activity.一个带有内部核糖体进入位点的大鼠脑双顺反子基因编码一种具有细胞毒性活性的苯环利定结合蛋白。
J Biol Chem. 2009 Jan 23;284(4):2245-57. doi: 10.1074/jbc.M807063200. Epub 2008 Nov 21.
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Effects of the gut microbiota on host adiposity are modulated by the short-chain fatty-acid binding G protein-coupled receptor, Gpr41.肠道微生物群对宿主肥胖的影响由短链脂肪酸结合G蛋白偶联受体Gpr41调节。
Proc Natl Acad Sci U S A. 2008 Oct 28;105(43):16767-72. doi: 10.1073/pnas.0808567105. Epub 2008 Oct 17.
7
Gpr40 is expressed in enteroendocrine cells and mediates free fatty acid stimulation of incretin secretion.Gpr40在肠内分泌细胞中表达,并介导游离脂肪酸对肠促胰岛素分泌的刺激作用。
Diabetes. 2008 Sep;57(9):2280-7. doi: 10.2337/db08-0307. Epub 2008 Jun 2.
8
Regulation of the gene encoding GPR40, a fatty acid receptor expressed selectively in pancreatic beta cells.对编码GPR40的基因的调控,GPR40是一种在胰腺β细胞中选择性表达的脂肪酸受体。
J Biol Chem. 2007 Aug 10;282(32):23561-71. doi: 10.1074/jbc.M702115200. Epub 2007 May 24.
9
GPR40 is necessary but not sufficient for fatty acid stimulation of insulin secretion in vivo.GPR40对于体内脂肪酸刺激胰岛素分泌是必要的,但并非充分条件。
Diabetes. 2007 Apr;56(4):1087-94. doi: 10.2337/db06-1532.
10
Short-chain fatty acid receptor, GPR43, is expressed by enteroendocrine cells and mucosal mast cells in rat intestine.短链脂肪酸受体GPR43在大鼠肠道的肠内分泌细胞和黏膜肥大细胞中表达。
Cell Tissue Res. 2006 Jun;324(3):353-60. doi: 10.1007/s00441-005-0140-x. Epub 2006 Feb 1.

GPR41 基因的表达是通过编码 GPR40 和 GPR41 蛋白的双顺反子 mRNA 的内部核糖体进入位点(IRES)依赖性翻译来介导的。

GPR41 gene expression is mediated by internal ribosome entry site (IRES)-dependent translation of bicistronic mRNA encoding GPR40 and GPR41 proteins.

机构信息

Department of Biological Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

J Biol Chem. 2012 Jun 8;287(24):20154-63. doi: 10.1074/jbc.M112.358887. Epub 2012 Apr 9.

DOI:10.1074/jbc.M112.358887
PMID:22493486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3370198/
Abstract

GPR41 is a G protein-coupled receptor activated by short chain fatty acids. The gene encoding GPR41 is located immediately downstream of a related gene encoding GPR40, a receptor for long chain fatty acids. Expression of GPR41 has been reported in a small number of cell types, including gut enteroendocrine cells and sympathetic ganglia, where it may play a role in the maintenance of metabolic homeostasis. We now demonstrate that GPR41, like GPR40, is expressed in pancreatic beta cells. Surprisingly, we found no evidence for transcriptional control elements or transcriptional initiation in the intergenic GPR40-GPR41 region. Rather, using 5'-rapid amplification of cDNA ends analysis, we demonstrated that GPR41 is transcribed from the promoter of the GPR40 gene. We confirmed this finding by generating bicistronic luciferase reporter plasmids, and we were able to map a potential internal ribosome entry site-containing region to a 2474-nucleotide region of the intergenic sequence. Consistent with this, we observed m(7)G cap-independent reporter gene expression upon transfection of RNA containing this region. Thus, GPR41 expression is mediated via an internal ribosome entry site located in the intergenic region of a bicistronic mRNA. This novel sequence organization may be utilized to permit coordinated regulation of the fatty acid receptors GPR40 and GPR41.

摘要

GPR41 是一种由短链脂肪酸激活的 G 蛋白偶联受体。编码 GPR41 的基因位于编码长链脂肪酸受体 GPR40 的基因的下游。GPR41 的表达已在少数细胞类型中报道,包括肠道内分泌细胞和交感神经节,在这些细胞中,它可能在维持代谢平衡中发挥作用。我们现在证明 GPR41 与 GPR40 一样在胰腺β细胞中表达。令人惊讶的是,我们在基因间 GPR40-GPR41 区域没有发现转录控制元件或转录起始的证据。相反,我们使用 5'-cDNA 末端快速扩增分析,证明 GPR41 是从 GPR40 基因的启动子转录的。我们通过生成双顺反子荧光素酶报告质粒证实了这一发现,并且我们能够将一个可能含有内部核糖体进入位点的区域映射到基因间序列的 2474 个核苷酸区域。与此一致,我们观察到在转染含有该区域的 RNA 时,m(7)G 帽非依赖性报告基因表达。因此,GPR41 的表达是通过位于双顺反子 mRNA 基因间区域的内部核糖体进入位点介导的。这种新的序列组织可能用于允许脂肪酸受体 GPR40 和 GPR41 的协调调节。