• 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

编码细胞骨架蛋白纽蛋白的人类基因的组织及纽蛋白启动子序列

Organization of the human gene encoding the cytoskeletal protein vinculin and the sequence of the vinculin promoter.

作者信息

Moiseyeva E P, Weller P A, Zhidkova N I, Corben E B, Patel B, Jasinska I, Koteliansky V E, Critchley D R

机构信息

Department of Biochemistry, University of Leicester, United Kingdom.

出版信息

J Biol Chem. 1993 Feb 25;268(6):4318-25.

PMID:8440716
Abstract

The human vinculin gene contains 22 exons ranging in size from 71 base pairs (bp) to 303 bp (average 155 bp) with the exception of exon 22 which contains 144 bp of coding sequence and 1848 bp of 3'-untranslated sequence including two polyadenylation signals. There is a limited correlation between exon boundaries and functional domains within the vinculin molecule. The talin-binding domain in vinculin spans residues 1-258, and the first 6 exons encode residues 1-261. Similarly, the predicted boundaries of the central repeat domain (residues 259-589) are close to the boundaries of exons 7 and 12. Analysis of vinculin mRNAs in human uterus showed that alternative splicing of the gene is limited to exon 19, which encodes the 68 amino acids included in the muscle-specific isoform called metavinculin. We have determined 1.1 kilobases of sequence 5' of the transcription start site. The vinculin promoter lacks a TATA box, but does contain six Sp1 sites, and a CArG box at position -262 which forms the core of the serum response element found in immediate-early response genes. Expression of a vinculin promoter/CAT construct is serum-inducible in NIH3T3 cells demonstrating that the promoter does contain a functional serum response element.

摘要

人类纽蛋白基因包含22个外显子,大小从71个碱基对(bp)到303 bp不等(平均155 bp),但外显子22除外,其包含144 bp的编码序列和1848 bp的3'非翻译序列,包括两个聚腺苷酸化信号。纽蛋白分子中外显子边界与功能域之间的相关性有限。纽蛋白中的踝蛋白结合结构域跨越第1至258位残基,前6个外显子编码第1至261位残基。同样,中央重复结构域(第259至589位残基)的预测边界接近外显子7和12的边界。对人子宫中纽蛋白mRNA的分析表明,该基因的可变剪接受限于外显子19,其编码肌肉特异性同种型中包含的68个氨基酸,称为间纽蛋白。我们已经确定了转录起始位点5'端1.1千碱基的序列。纽蛋白启动子缺乏TATA框,但确实包含六个Sp1位点,以及位于-262位置的一个CArG框,它构成了立即早期反应基因中发现的血清反应元件的核心。纽蛋白启动子/CAT构建体在NIH3T3细胞中可被血清诱导表达,表明该启动子确实包含一个功能性血清反应元件。

相似文献

1
Organization of the human gene encoding the cytoskeletal protein vinculin and the sequence of the vinculin promoter.编码细胞骨架蛋白纽蛋白的人类基因的组织及纽蛋白启动子序列
J Biol Chem. 1993 Feb 25;268(6):4318-25.
2
The mouse p44 mitogen-activated protein kinase (extracellular signal-regulated kinase 1) gene. Genomic organization and structure of the 5'-flanking regulatory region.小鼠p44丝裂原活化蛋白激酶(细胞外信号调节激酶1)基因。5'侧翼调控区的基因组组织与结构。
J Biol Chem. 1995 Nov 10;270(45):26986-92. doi: 10.1074/jbc.270.45.26986.
3
Structure and expression of the mouse growth hormone receptor/growth hormone binding protein gene.小鼠生长激素受体/生长激素结合蛋白基因的结构与表达
J Mol Endocrinol. 1999 Aug;23(1):33-44. doi: 10.1677/jme.0.0230033.
4
Characterization of the human bone sialoprotein (BSP) gene and its promoter sequence.人类骨唾液蛋白(BSP)基因及其启动子序列的特征分析。
Matrix Biol. 1994 Jan;14(1):31-40. doi: 10.1016/0945-053x(94)90027-2.
5
The genomic structure of the human SPEC1 gene reveals complex splicing and close promoter proximity to the AF1q translocation gene.人类SPEC1基因的基因组结构显示出复杂的剪接方式,且其启动子与AF1q易位基因紧密相邻。
Gene. 2001 Aug 8;273(2):295-303. doi: 10.1016/s0378-1119(01)00561-3.
6
An additional exon in the human vinculin gene specifically encodes meta-vinculin-specific difference peptide. Cross-species comparison reveals variable and conserved motifs in the meta-vinculin insert.
Eur J Biochem. 1992 Mar 1;204(2):767-72. doi: 10.1111/j.1432-1033.1992.tb16692.x.
7
Organization of the mouse microfibril-associated glycoprotein-2 (MAGP-2) gene.小鼠微原纤维相关糖蛋白2(MAGP-2)基因的组织
Mamm Genome. 2000 Mar;11(3):191-5. doi: 10.1007/s003350010036.
8
Genomic organization and alternative splicing of human PACE4 (SPC4), kexin-like processing endoprotease.人类PACE4(SPC4)的基因组结构与可变剪接,类克新加工内切蛋白酶
J Biochem. 1997 Aug;122(2):438-52. doi: 10.1093/oxfordjournals.jbchem.a021772.
9
Cloning and analysis of the promoter region of the rat SM22 alpha gene.大鼠SM22α基因启动子区域的克隆与分析
Biochem J. 1995 Sep 15;310 ( Pt 3)(Pt 3):1037-43. doi: 10.1042/bj3101037.
10
Complete structure of the murine p36 (annexin II) gene. Identification of mRNAs for both the murine and the human gene with alternatively spliced 5' noncoding exons.小鼠p36(膜联蛋白II)基因的完整结构。鉴定小鼠和人类基因带有可变剪接5'非编码外显子的mRNA。
Biochim Biophys Acta. 1996 May 2;1306(2-3):160-70. doi: 10.1016/0167-4781(95)00238-3.

引用本文的文献

1
Unveiling the Spectrum of Minor Genes in Cardiomyopathies: A Narrative Review.揭示心肌病中小基因的谱:一篇叙述性综述。
Int J Mol Sci. 2024 Sep 10;25(18):9787. doi: 10.3390/ijms25189787.
2
Understanding the molecular basis of cardiomyopathy.了解心肌病的分子基础。
Am J Physiol Heart Circ Physiol. 2022 Feb 1;322(2):H181-H233. doi: 10.1152/ajpheart.00562.2021. Epub 2021 Nov 19.
3
SRF phosphorylation by glycogen synthase kinase-3 promotes axon growth in hippocampal neurons.糖原合成酶激酶-3 对 SRF 的磷酸化促进海马神经元的轴突生长。
J Neurosci. 2014 Mar 12;34(11):4027-42. doi: 10.1523/JNEUROSCI.4677-12.2014.
4
Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant.家族性扩张型心肌病与先天性缺陷相关,伴有一种新的VCL突变(Lys815Arg)以及一种已知的MYPBC3变异。
Cardiogenetics. 2011 Aug 22;1(1). doi: 10.4081/cardiogenetics.2011.e10.
5
Vinculin, cadherin mechanotransduction and homeostasis of cell-cell junctions.着丝粒蛋白、钙黏蛋白机械转导与细胞-细胞连接的稳态。
Protoplasma. 2013 Aug;250(4):817-29. doi: 10.1007/s00709-012-0475-6. Epub 2012 Dec 29.
6
Degeneration of the mouse retina upon dysregulated activity of serum response factor.血清反应因子活性失调导致小鼠视网膜退化。
Mol Vis. 2011 Apr 29;17:1110-27.
7
The vinculin-DeltaIn20/21 mouse: characteristics of a constitutive, actin-binding deficient splice variant of vinculin.连接蛋白-DeltaIn20/21 小鼠:连接蛋白的一种组成型、肌动蛋白结合缺陷的剪接变异体的特征。
PLoS One. 2010 Jul 14;5(7):e11530. doi: 10.1371/journal.pone.0011530.
8
Cardiac-myocyte-specific excision of the vinculin gene disrupts cellular junctions, causing sudden death or dilated cardiomyopathy.纽蛋白基因在心肌细胞中的特异性切除会破坏细胞连接,导致猝死或扩张型心肌病。
Mol Cell Biol. 2007 Nov;27(21):7522-37. doi: 10.1128/MCB.00728-07. Epub 2007 Sep 4.
9
Heterozygous inactivation of the vinculin gene predisposes to stress-induced cardiomyopathy.纽蛋白基因的杂合失活易引发应激性心肌病。
Am J Pathol. 2004 Sep;165(3):1033-44. doi: 10.1016/S0002-9440(10)63364-0.
10
Expression profiling of serum inducible genes identifies a subset of SRF target genes that are MKL dependent.血清诱导基因的表达谱分析鉴定出一组受血清反应因子(SRF)调控且依赖于肌动蛋白结合蛋白(MKL)的靶基因。
BMC Mol Biol. 2004 Aug 25;5:13. doi: 10.1186/1471-2199-5-13.