• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人类内向整流钾离子通道亚基kir5.1(KCNJ16)定位于17号染色体长臂25区,在肾脏和胰腺中表达。

The human inward rectifier K(+) channel subunit kir5.1 (KCNJ16) maps to chromosome 17q25 and is expressed in kidney and pancreas.

作者信息

Liu Y, McKenna E, Figueroa D J, Blevins R, Austin C P, Bennett P B, Swanson R

机构信息

Department of Bioinformatics, Merck & Co., West Point, PA 19486, USA.

出版信息

Cytogenet Cell Genet. 2000;90(1-2):60-3. doi: 10.1159/000015662.

DOI:10.1159/000015662
PMID:11060447
Abstract

A novel human Kir5.1 (inward rectifier K+ channel subunit, gene name KCNJ16) was identified through database searches. This human KCNJ16 was mapped to chromosome 17q25. The full-length cDNA was identified and its genomic structure was determined. Tissue distribution studies showed that human KCNJ16 is significantly expressed in human kidney, pancreas and thyroid gland. In situ hybridization revealed expression in convoluted tubule cells of kidney and in the acinar and ductal cells of pancreas. These suggest that human Kir5.1 may be involved in the regulation of fluid and pH balance, thus making it a potential therapeutic target for hypertension, renal failure, or pancreatic disease.

摘要

通过数据库搜索鉴定出一种新型人类Kir5.1(内向整流钾离子通道亚基,基因名称为KCNJ16)。该人类KCNJ16基因定位于17号染色体q25区域。鉴定出了全长cDNA并确定了其基因组结构。组织分布研究表明,人类KCNJ16在人肾、胰腺和甲状腺中显著表达。原位杂交显示在肾曲小管细胞以及胰腺腺泡和导管细胞中有表达。这些表明人类Kir5.1可能参与了液体和pH平衡的调节,因此使其成为高血压、肾衰竭或胰腺疾病的潜在治疗靶点。

相似文献

1
The human inward rectifier K(+) channel subunit kir5.1 (KCNJ16) maps to chromosome 17q25 and is expressed in kidney and pancreas.人类内向整流钾离子通道亚基kir5.1(KCNJ16)定位于17号染色体长臂25区,在肾脏和胰腺中表达。
Cytogenet Cell Genet. 2000;90(1-2):60-3. doi: 10.1159/000015662.
2
Genetic and functional linkage of Kir5.1 and Kir2.1 channel subunits.Kir5.1和Kir2.1通道亚基的遗传与功能联系。
FEBS Lett. 2001 Mar 2;491(3):305-11. doi: 10.1016/s0014-5793(01)02202-5.
3
Cloning and characterization of two K+ inward rectifier (Kir) 1.1 potassium channel homologs from human kidney (Kir1.2 and Kir1.3).从人肾中克隆并鉴定两个钾离子内向整流通道(Kir)1.1钾通道同源物(Kir1.2和Kir1.3)
J Biol Chem. 1997 Jan 3;272(1):586-93. doi: 10.1074/jbc.272.1.586.
4
Cloning, functional expression and mRNA distribution of an inwardly rectifying potassium channel protein.
FEBS Lett. 1995 Jun 26;367(2):127-31. doi: 10.1016/0014-5793(95)00527-g.
5
Deletion of Kir5.1 Impairs Renal Ability to Excrete Potassium during Increased Dietary Potassium Intake.钾摄入增加时,Kir5.1 的缺失可损害肾脏排钾能力。
J Am Soc Nephrol. 2019 Aug;30(8):1425-1438. doi: 10.1681/ASN.2019010025. Epub 2019 Jun 25.
6
Diverse functions of the inward-rectifying potassium channel Kir5.1 and its relationship with human diseases.内向整流钾通道Kir5.1的多种功能及其与人类疾病的关系。
Front Physiol. 2023 Feb 27;14:1127893. doi: 10.3389/fphys.2023.1127893. eCollection 2023.
7
A novel ATP-dependent inward rectifier potassium channel expressed predominantly in glial cells.一种主要在神经胶质细胞中表达的新型ATP依赖性内向整流钾通道。
J Biol Chem. 1995 Jul 7;270(27):16339-46. doi: 10.1074/jbc.270.27.16339.
8
Cloning, localization, and functional expression of a human brain inward rectifier potassium channel (hIRK1).一种人类脑内向整流钾通道(hIRK1)的克隆、定位及功能表达
Recept Channels. 1995;3(3):175-83.
9
Expression of adenosine triphosphate-sensitive potassium channel subunits in female rat reproductive tissues: overlapping distribution of messenger ribonucleic acid for weak inwardly rectifying potassium channel subunit 6.1 and sulfonylurea-binding regulatory subunit 2.三磷酸腺苷敏感性钾通道亚基在雌性大鼠生殖组织中的表达:内向整流性钾通道亚基6.1与磺脲类结合调节亚基2信使核糖核酸的重叠分布
Am J Obstet Gynecol. 1999 May;180(5):1121-6. doi: 10.1016/s0002-9378(99)70604-6.
10
In vivo formation of a proton-sensitive K+ channel by heteromeric subunit assembly of Kir5.1 with Kir4.1.通过Kir5.1与Kir4.1的异源亚基组装在体内形成质子敏感钾通道。
J Physiol. 2000 Jun 15;525 Pt 3(Pt 3):587-92. doi: 10.1111/j.1469-7793.2000.00587.x.

引用本文的文献

1
The physiological characteristics of inward rectifying potassium channel Kir4.2 and its research progress in human diseases.内向整流钾通道Kir4.2的生理特性及其在人类疾病中的研究进展
Front Cell Dev Biol. 2025 Apr 24;13:1519080. doi: 10.3389/fcell.2025.1519080. eCollection 2025.
2
Novel KCNJ16 variants identified in a Chinese patient with hypokalemic metabolic acidosis.在中国低钾代谢性酸中毒患者中发现的新型 KCNJ16 变异体。
Mol Genet Genomic Med. 2023 Nov;11(11):e2238. doi: 10.1002/mgg3.2238. Epub 2023 Jul 19.
3
Diverse functions of the inward-rectifying potassium channel Kir5.1 and its relationship with human diseases.
内向整流钾通道Kir5.1的多种功能及其与人类疾病的关系。
Front Physiol. 2023 Feb 27;14:1127893. doi: 10.3389/fphys.2023.1127893. eCollection 2023.
4
Kir5.1 channels: potential role in epilepsy and seizure disorders.Kir5.1 通道:在癫痫和癫痫发作障碍中的潜在作用。
Am J Physiol Cell Physiol. 2022 Sep 1;323(3):C706-C717. doi: 10.1152/ajpcell.00235.2022. Epub 2022 Jul 18.
5
Inwardly rectifying potassium channel 5.1: Structure, function, and possible roles in diseases.内向整流钾通道5.1:结构、功能及在疾病中的可能作用
Genes Dis. 2020 Mar 21;8(3):272-278. doi: 10.1016/j.gendis.2020.03.006. eCollection 2021 May.
6
Ion Channel Signature in Healthy Pancreas and Pancreatic Ductal Adenocarcinoma.健康胰腺和胰腺导管腺癌中的离子通道特征
Front Pharmacol. 2020 Oct 16;11:568993. doi: 10.3389/fphar.2020.568993. eCollection 2020.
7
Contrasting signatures of genomic divergence during sympatric speciation.同域物种形成过程中基因组分歧的鲜明特征。
Nature. 2020 Dec;588(7836):106-111. doi: 10.1038/s41586-020-2845-0. Epub 2020 Oct 28.
8
Potassium channels in pancreatic duct epithelial cells: their role, function and pathophysiological relevance.胰腺导管上皮细胞中的钾通道:它们的作用、功能及病理生理相关性。
Pflugers Arch. 2015 Apr;467(4):625-40. doi: 10.1007/s00424-014-1585-0. Epub 2014 Jul 31.
9
A high-coverage genome sequence from an archaic Denisovan individual.古丹尼索瓦人个体的高覆盖度基因组序列。
Science. 2012 Oct 12;338(6104):222-6. doi: 10.1126/science.1224344. Epub 2012 Aug 30.
10
Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.全基因组关联研究在 17q24.3 鉴定出甲状腺功能亢进性周期性瘫痪的易感性位点。
Nat Genet. 2012 Sep;44(9):1026-9. doi: 10.1038/ng.2367. Epub 2012 Aug 5.