• 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

相似文献

1
Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy.突触结合蛋白 2 突变导致常染色体显性遗传的 Lambert-Eaton 肌无力综合征和非进行性运动神经病。
Am J Hum Genet. 2014 Sep 4;95(3):332-9. doi: 10.1016/j.ajhg.2014.08.007.
2
Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations.由 SYT2 突变引起的显性和隐性先天性肌无力综合征。
Muscle Nerve. 2021 Aug;64(2):219-224. doi: 10.1002/mus.27332. Epub 2021 Jun 12.
3
How to Spot Congenital Myasthenic Syndromes Resembling the Lambert-Eaton Myasthenic Syndrome? A Brief Review of Clinical, Electrophysiological, and Genetics Features.如何发现类似于 Lambert-Eaton 肌无力综合征的先天性肌无力综合征?临床、电生理和遗传学特征的简要综述。
Neuromolecular Med. 2018 Jun;20(2):205-214. doi: 10.1007/s12017-018-8490-1. Epub 2018 Apr 25.
4
Recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly conserved C-terminal amino acid sequence.隐性先天性肌病综合征由 SYT2 中的纯合突变引起,该突变改变了高度保守的 C 末端氨基酸序列。
Am J Med Genet A. 2020 Jul;182(7):1744-1749. doi: 10.1002/ajmg.a.61579. Epub 2020 Apr 6.
5
Biallelic loss of function variants in SYT2 cause a treatable congenital onset presynaptic myasthenic syndrome.SYT2 中的双等位基因功能丧失变异导致可治疗的先天性发作性 presynaptic 肌无力综合征。
Am J Med Genet A. 2020 Oct;182(10):2272-2283. doi: 10.1002/ajmg.a.61765. Epub 2020 Aug 10.
6
A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular junction dysfunction?一种新的散发型 SYT2 突变,表现为远端肌无力。神经病还是神经肌肉接头功能障碍?
J Peripher Nerv Syst. 2021 Mar;26(1):113-117. doi: 10.1111/jns.12425. Epub 2020 Dec 22.
7
Synaptotagmin can cause an immune-mediated model of Lambert-Eaton myasthenic syndrome in rats.突触结合蛋白可在大鼠中引发兰伯特-伊顿肌无力综合征的免疫介导模型。
Ann Neurol. 1994 Jan;35(1):74-80. doi: 10.1002/ana.410350112.
8
Electrophysiologic features of SYT2 mutations causing a treatable neuromuscular syndrome.导致可治疗性神经肌肉综合征的SYT2突变的电生理特征
Neurology. 2015 Dec 1;85(22):1964-71. doi: 10.1212/WNL.0000000000002185. Epub 2015 Oct 30.
9
Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome.果蝇研究支持突触前突触结合蛋白突变在人类先天性肌无力综合征中的作用。
PLoS One. 2017 Sep 27;12(9):e0184817. doi: 10.1371/journal.pone.0184817. eCollection 2017.
10
Identification of a new SYT2 variant validates an unusual distal motor neuropathy phenotype.一种新的SYT2变体的鉴定证实了一种罕见的远端运动神经病表型。
Neurol Genet. 2018 Oct 22;4(6):e282. doi: 10.1212/NXG.0000000000000282. eCollection 2018 Dec.

引用本文的文献

1
Review of 40 genes causing congenital myasthenic syndromes.40种导致先天性肌无力综合征的基因综述。
J Hum Genet. 2025 Jun 18. doi: 10.1038/s10038-025-01355-9.
2
Dynamic formation of the protein-lipid prefusion complex.蛋白质-脂类预融合复合物的动态形成。
Biophys J. 2024 Oct 15;123(20):3569-3586. doi: 10.1016/j.bpj.2024.09.009. Epub 2024 Sep 10.
3
Amifampridines are the Most Effective Drugs for Treating Lambert-Eaton Myasthenic Syndrome With a Focus on Pediatric Lambert-Eaton Myasthenic Syndrome.氨吡啶类药物是治疗兰伯特-伊顿肌无力综合征最有效的药物,重点关注儿童兰伯特-伊顿肌无力综合征。
J Clin Neurol. 2024 Jul;20(4):353-361. doi: 10.3988/jcn.2024.0018.
4
A cell type-specific approach to elucidate the role of miR-96 in inner ear hair cells.一种用于阐明miR-96在内耳毛细胞中作用的细胞类型特异性方法。
Front Audiol Otol. 2024;2. doi: 10.3389/fauot.2024.1400576. Epub 2024 May 9.
5
Dynamic Formation of the Protein-Lipid Pre-fusion Complex.蛋白质-脂质预融合复合物的动态形成
bioRxiv. 2024 May 11:2024.04.17.589983. doi: 10.1101/2024.04.17.589983.
6
Calcium Sensors of Neurotransmitter Release.神经递质释放的钙传感器。
Adv Neurobiol. 2023;33:119-138. doi: 10.1007/978-3-031-34229-5_5.
7
Presynaptic Congenital Myasthenic Syndromes: Understanding Clinical Phenotypes through In vivo Models.突触前先天性肌无力综合征:通过体内模型理解临床表型。
J Neuromuscul Dis. 2023;10(5):731-759. doi: 10.3233/JND-221646.
8
Simulations of active zone structure and function at mammalian NMJs predict that loss of calcium channels alone is not sufficient to replicate LEMS effects.哺乳动物 NMJ 上的活性区结构和功能模拟预测,仅丧失钙通道不足以复制 LEMS 的作用。
J Neurophysiol. 2023 May 1;129(5):1259-1277. doi: 10.1152/jn.00404.2022. Epub 2023 Apr 19.
9
Neuromuscular junction involvement in inherited motor neuropathies: genetic heterogeneity and effect of oral salbutamol treatment.遗传性运动神经病中的神经肌肉接头受累:遗传异质性和口服沙丁胺醇治疗的效果。
J Neurol. 2023 Jun;270(6):3112-3119. doi: 10.1007/s00415-023-11643-z. Epub 2023 Mar 4.
10
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review.先天性肌营养不良症的临床与病理特征 35 个基因-全面综述。
Int J Mol Sci. 2023 Feb 13;24(4):3730. doi: 10.3390/ijms24043730.

本文引用的文献

1
Genic intolerance to functional variation and the interpretation of personal genomes.遗传不耐受功能性变异与个人基因组解读
PLoS Genet. 2013;9(8):e1003709. doi: 10.1371/journal.pgen.1003709. Epub 2013 Aug 22.
2
GEnomes Management Application (GEM.app): a new software tool for large-scale collaborative genome analysis.基因组管理应用程序(GEM.app):用于大规模协作基因组分析的新软件工具。
Hum Mutat. 2013 Jun;34(6):842-6. doi: 10.1002/humu.22305. Epub 2013 Apr 3.
3
Genetic analysis of synaptotagmin C2 domain specificity in regulating spontaneous and evoked neurotransmitter release.突触结合蛋白 C2 结构域特异性在调节自发性和诱发性神经递质释放中的遗传分析。
J Neurosci. 2013 Jan 2;33(1):187-200. doi: 10.1523/JNEUROSCI.3214-12.2013.
4
Complexin controls spontaneous and evoked neurotransmitter release by regulating the timing and properties of synaptotagmin activity.复合蛋白通过调节突触结合蛋白活性的时间和特性来控制神经递质的自发和诱发释放。
J Neurosci. 2012 Dec 12;32(50):18234-45. doi: 10.1523/JNEUROSCI.3212-12.2012.
5
Defective presynaptic choline transport underlies hereditary motor neuropathy.遗传性运动神经病的根本原因是突触前胆碱转运缺陷。
Am J Hum Genet. 2012 Dec 7;91(6):1103-7. doi: 10.1016/j.ajhg.2012.09.019. Epub 2012 Nov 8.
6
Titin mutation segregates with hereditary myopathy with early respiratory failure.肌联蛋白突变与遗传性肌病伴早期呼吸衰竭相关。
Brain. 2012 Jun;135(Pt 6):1695-713. doi: 10.1093/brain/aws102. Epub 2012 May 9.
7
Lambert-Eaton myasthenic syndrome: from clinical characteristics to therapeutic strategies. Lambert-Eaton 肌无力综合征:从临床特征到治疗策略。
Lancet Neurol. 2011 Dec;10(12):1098-107. doi: 10.1016/S1474-4422(11)70245-9.
8
Distinct roles for two synaptotagmin isoforms in synchronous and asynchronous transmitter release at zebrafish neuromuscular junction.两种突触结合蛋白异构体在斑马鱼神经肌肉接头中同步和异步递质释放中的不同作用。
Proc Natl Acad Sci U S A. 2010 Aug 3;107(31):13906-11. doi: 10.1073/pnas.1008598107. Epub 2010 Jul 19.
9
Synaptotagmin-2 is essential for survival and contributes to Ca2+ triggering of neurotransmitter release in central and neuromuscular synapses.突触结合蛋白-2对生存至关重要,并有助于在中枢和神经肌肉突触中由钙离子触发神经递质释放。
J Neurosci. 2006 Dec 27;26(52):13493-504. doi: 10.1523/JNEUROSCI.3519-06.2006.
10
Visualization of synaptotagmin I oligomers assembled onto lipid monolayers.可视化组装在脂质单分子层上的突触结合蛋白I寡聚体。
Proc Natl Acad Sci U S A. 2003 Feb 18;100(4):2082-7. doi: 10.1073/pnas.0435872100. Epub 2003 Feb 10.

突触结合蛋白 2 突变导致常染色体显性遗传的 Lambert-Eaton 肌无力综合征和非进行性运动神经病。

Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy.

机构信息

Department of Neurology, University of Rochester Medical Center, Rochester, NY 14642, USA.

Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK.

出版信息

Am J Hum Genet. 2014 Sep 4;95(3):332-9. doi: 10.1016/j.ajhg.2014.08.007.

DOI:10.1016/j.ajhg.2014.08.007
PMID:25192047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4157148/
Abstract

Synaptotagmin 2 is a synaptic vesicle protein that functions as a calcium sensor for neurotransmission but has not been previously associated with human disease. Via whole-exome sequencing, we identified heterozygous missense mutations in the C2B calcium-binding domain of the gene encoding Synaptotagmin 2 in two multigenerational families presenting with peripheral motor neuron syndromes. An essential calcium-binding aspartate residue, Asp307Ala, was disrupted by a c.920A>C change in one family that presented with an autosomal-dominant presynaptic neuromuscular junction disorder resembling Lambert-Eaton myasthenic syndrome. A c.923C>T variant affecting an adjacent residue (p.Pro308Leu) produced a presynaptic neuromuscular junction defect and a dominant hereditary motor neuropathy in a second family. Characterization of the mutation homologous to the human c.920A>C variant in Drosophila Synaptotagmin revealed a dominant disruption of synaptic vesicle exocytosis using this transgenic model. These findings indicate that Synaptotagmin 2 regulates neurotransmitter release at human peripheral motor nerve terminals. In addition, mutations in the Synaptotagmin 2 C2B domain represent an important cause of presynaptic congenital myasthenic syndromes and link them with hereditary motor axonopathies.

摘要

突触融合蛋白 2 是一种突触囊泡蛋白,作为神经递质传递的钙传感器发挥作用,但以前与人类疾病无关。通过全外显子组测序,我们在两个呈现周围运动神经元综合征的多代家族中鉴定出编码突触融合蛋白 2 的基因的 C2B 钙结合域中的杂合错义突变。一个家族中发生了 c.920A>C 变化,破坏了一个关键的钙结合天冬氨酸残基 Asp307Ala,该家族表现出类似于 Lambert-Eaton 肌无力综合征的常染色体显性突触前神经肌肉接头障碍。另一个家族中,c.923C>T 变体影响相邻残基(p.Pro308Leu),导致突触前神经肌肉接头缺陷和显性遗传性运动神经病。在果蝇突触融合蛋白中对与人类 c.920A>C 变体同源的突变进行表征,发现该转基因模型中突触囊泡胞吐作用的显性破坏。这些发现表明突触融合蛋白 2 调节人类周围运动神经末梢的神经递质释放。此外,突触融合蛋白 2 C2B 结构域的突变代表了突触前先天性肌无力综合征的一个重要原因,并将其与遗传性运动轴索性神经病联系起来。