• 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

KCNQ2钾通道转录本的可变剪接有助于M电流的功能多样性。

Alternative splicing of KCNQ2 potassium channel transcripts contributes to the functional diversity of M-currents.

作者信息

Pan Z, Selyanko A A, Hadley J K, Brown D A, Dixon J E, McKinnon D

机构信息

Department of Neurobiology and Behavior and Department of Physiology and Biophysics, State University of New York at Stony Brook, Stony Brook, NY 11794, USA.

出版信息

J Physiol. 2001 Mar 1;531(Pt 2):347-58. doi: 10.1111/j.1469-7793.2001.0347i.x.

DOI:10.1111/j.1469-7793.2001.0347i.x
PMID:11230508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2278468/
Abstract

The region of alternative splicing in the KCNQ2 potassium channel gene was determined by RNase protection analysis of KCNQ2 mRNA transcripts. Systematic analysis of KCNQ2 alternative splice variant expression in rat superior cervical ganglia revealed multiple variant isoforms. One class of KCNQ2 splice variants, those that contained exon 15a, was found to have significantly different kinetics to those of the other isoforms. These transcripts encoded channel subunits that, when co-expressed with the KCNQ3 subunit, activated and deactivated approximately 2.5 times more slowly than other isoforms. Deletion of exon 15a in these isoforms produced a reversion to the faster kinetics. Comparison of the kinetic properties of the cloned channel splice variants with those of the native M-current suggests that alternative splicing of the KCNQ2 gene may contribute to the variation in M-current kinetics seen in vivo.

摘要

通过对KCNQ2 mRNA转录本进行核糖核酸酶保护分析,确定了KCNQ2钾通道基因中的可变剪接区域。对大鼠颈上神经节中KCNQ2可变剪接变体表达的系统分析揭示了多种变体亚型。发现一类包含外显子15a的KCNQ2剪接变体,其动力学与其他亚型有显著差异。这些转录本编码的通道亚基,在与KCNQ3亚基共表达时,激活和失活的速度比其他亚型慢约2.5倍。在这些亚型中删除外显子15a会使动力学恢复到更快的状态。将克隆的通道剪接变体的动力学特性与天然M电流的动力学特性进行比较表明,KCNQ2基因的可变剪接可能导致体内M电流动力学的变化。

相似文献

1
Alternative splicing of KCNQ2 potassium channel transcripts contributes to the functional diversity of M-currents.KCNQ2钾通道转录本的可变剪接有助于M电流的功能多样性。
J Physiol. 2001 Mar 1;531(Pt 2):347-58. doi: 10.1111/j.1469-7793.2001.0347i.x.
2
Stoichiometry of expressed KCNQ2/KCNQ3 potassium channels and subunit composition of native ganglionic M channels deduced from block by tetraethylammonium.由四乙铵阻断推导表达的KCNQ2/KCNQ3钾通道的化学计量和天然神经节M通道的亚基组成。
J Neurosci. 2003 Jun 15;23(12):5012-9. doi: 10.1523/JNEUROSCI.23-12-05012.2003.
3
Subunit-specific modulation of KCNQ potassium channels by Src tyrosine kinase.Src 酪氨酸激酶对 KCNQ 钾通道的亚基特异性调节。
J Neurosci. 2003 Jan 1;23(1):84-95. doi: 10.1523/JNEUROSCI.23-01-00084.2003.
4
The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3.KCNQ2钾通道:剪接变体、功能及发育表达。脑定位及与KCNQ3的比较。
FEBS Lett. 1998 Nov 6;438(3):171-6. doi: 10.1016/s0014-5793(98)01296-4.
5
Reconstitution of muscarinic modulation of the KCNQ2/KCNQ3 K(+) channels that underlie the neuronal M current.构成神经元M电流基础的KCNQ2/KCNQ3钾通道的毒蕈碱调节的重构。
J Neurosci. 2000 Mar 1;20(5):1710-21. doi: 10.1523/JNEUROSCI.20-05-01710.2000.
6
Antibodies and a cysteine-modifying reagent show correspondence of M current in neurons to KCNQ2 and KCNQ3 K+ channels.抗体和一种半胱氨酸修饰试剂表明神经元中的M电流与KCNQ2和KCNQ3钾离子通道存在对应关系。
Br J Pharmacol. 2002 Dec;137(8):1173-86. doi: 10.1038/sj.bjp.0704989.
7
Differential expression of kcnq2 splice variants: implications to m current function during neuronal development.KCNQ2剪接变体的差异表达:对神经元发育过程中M电流功能的影响。
J Neurosci. 2001 Feb 15;21(4):1096-103. doi: 10.1523/JNEUROSCI.21-04-01096.2001.
8
Two types of K(+) channel subunit, Erg1 and KCNQ2/3, contribute to the M-like current in a mammalian neuronal cell.两种钾离子通道亚基,即Erg1和KCNQ2/3,对哺乳动物神经元细胞中的M样电流有贡献。
J Neurosci. 1999 Sep 15;19(18):7742-56. doi: 10.1523/JNEUROSCI.19-18-07742.1999.
9
Properties of single M-type KCNQ2/KCNQ3 potassium channels expressed in mammalian cells.在哺乳动物细胞中表达的单个M型KCNQ2/KCNQ3钾通道的特性。
J Physiol. 2001 Jul 1;534(Pt 1):15-24. doi: 10.1111/j.1469-7793.2001.00015.x.
10
Mechanisms underlying modulation of neuronal KCNQ2/KCNQ3 potassium channels by extracellular protons.细胞外质子对神经元KCNQ2/KCNQ3钾通道的调节机制。
J Gen Physiol. 2003 Dec;122(6):775-93. doi: 10.1085/jgp.200308897.

引用本文的文献

1
Plural molecular and cellular mechanisms of pore domain encephalopathy.孔域脑病的多种分子和细胞机制。
Elife. 2025 Jan 6;13:RP91204. doi: 10.7554/eLife.91204.
2
Plural molecular and cellular mechanisms of pore domain encephalopathy.孔结构域脑病的多种分子和细胞机制。
bioRxiv. 2024 Jun 26:2024.01.04.574177. doi: 10.1101/2024.01.04.574177.
3
Heteromeric Kv7.2/7.3 channels differentially regulate action potential initiation and conduction in neocortical myelinated axons.异源 Kv7.2/7.3 通道在新皮层有髓轴突中差异调节动作电位起始和传导。
J Neurosci. 2014 Mar 5;34(10):3719-32. doi: 10.1523/JNEUROSCI.4206-13.2014.
4
Activation of axonal Kv7 channels in human peripheral nerve by flupirtine but not placebo - therapeutic potential for peripheral neuropathies: results of a randomised controlled trial.氟吡汀而非安慰剂激活人外周神经中的轴突 Kv7 通道-治疗周围神经病变的潜力:一项随机对照试验的结果。
J Transl Med. 2013 Feb 8;11:34. doi: 10.1186/1479-5876-11-34.
5
Relating ion channel expression, bifurcation structure, and diverse firing patterns in a model of an identified motor neuron.在一个已识别的运动神经元模型中关联离子通道表达、分支结构和多样的放电模式。
J Comput Neurosci. 2013 Apr;34(2):211-29. doi: 10.1007/s10827-012-0416-6. Epub 2012 Aug 11.
6
Transcriptional repression of the M channel subunit Kv7.2 in chronic nerve injury.慢性神经损伤中 M 通道亚基 Kv7.2 的转录抑制。
Pain. 2011 Apr;152(4):742-754. doi: 10.1016/j.pain.2010.12.028. Epub 2011 Feb 23.
7
New tricks for old dogs: KCNQ expression and role in smooth muscle.老狗也有新把戏:KCNQ 表达及其在平滑肌中的作用。
Br J Pharmacol. 2009 Apr;156(8):1196-203. doi: 10.1111/j.1476-5381.2009.00131.x.
8
Ion channel clustering at the axon initial segment and node of Ranvier evolved sequentially in early chordates.离子通道在轴突起始段和郎飞结处的聚集在早期脊索动物中是依次进化的。
PLoS Genet. 2008 Dec;4(12):e1000317. doi: 10.1371/journal.pgen.1000317. Epub 2008 Dec 26.
9
Expression and localization of K channels KCNQ2 and KCNQ3 in the mammalian cochlea.钾通道KCNQ2和KCNQ3在哺乳动物耳蜗中的表达与定位
Audiol Neurootol. 2009;14(2):98-105. doi: 10.1159/000158538. Epub 2008 Oct 1.
10
KCNQ/M-currents contribute to the resting membrane potential in rat visceral sensory neurons.钾离子通道蛋白Q/M电流有助于大鼠内脏感觉神经元的静息膜电位。
J Physiol. 2006 Aug 15;575(Pt 1):175-89. doi: 10.1113/jphysiol.2006.113308. Epub 2006 Jun 15.

本文引用的文献

1
Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors.通过M1毒蕈碱型乙酰胆碱受体抑制哺乳动物细胞中表达的KCNQ1 - 4钾通道。
J Physiol. 2000 Feb 1;522 Pt 3(Pt 3):349-55. doi: 10.1111/j.1469-7793.2000.t01-2-00349.x.
2
A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly.KCNQ1通道的一种隐性C末端耶尔韦尔和朗格-尼尔森突变会损害亚基组装。
EMBO J. 2000 Feb 1;19(3):332-40. doi: 10.1093/emboj/19.3.332.
3
Two types of K(+) channel subunit, Erg1 and KCNQ2/3, contribute to the M-like current in a mammalian neuronal cell.两种钾离子通道亚基,即Erg1和KCNQ2/3,对哺乳动物神经元细胞中的M样电流有贡献。
J Neurosci. 1999 Sep 15;19(18):7742-56. doi: 10.1523/JNEUROSCI.19-18-07742.1999.
4
M-channel gating and simulation.M通道门控与模拟
Biophys J. 1999 Aug;77(2):701-13. doi: 10.1016/S0006-3495(99)76925-0.
5
Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions.
Hum Genet. 1999 Mar;104(3):234-40. doi: 10.1007/pl00008713.
6
KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel.KCNQ2和KCNQ3钾通道亚基:M通道的分子关联
Science. 1998 Dec 4;282(5395):1890-3. doi: 10.1126/science.282.5395.1890.
7
The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3.KCNQ2钾通道:剪接变体、功能及发育表达。脑定位及与KCNQ3的比较。
FEBS Lett. 1998 Nov 6;438(3):171-6. doi: 10.1016/s0014-5793(98)01296-4.
8
KQT2, a new putative potassium channel family produced by alternative splicing. Isolation, genomic structure, and alternative splicing of the putative potassium channels.
Recept Channels. 1998;5(5):255-71.
9
A potassium channel mutation in neonatal human epilepsy.新生儿人类癫痫中的一种钾通道突变。
Science. 1998 Jan 16;279(5349):403-6. doi: 10.1126/science.279.5349.403.
10
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.一个特发性癫痫家族中一个新型KQT样钾通道基因的孔突变。
Nat Genet. 1998 Jan;18(1):53-5. doi: 10.1038/ng0198-53.