• 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

心脏同源盒基因CSX定位于人类染色体5q34。

Assignment of cardiac homeobox gene CSX to human chromosome 5q34.

作者信息

Shiojima I, Komuro I, Inazawa J, Nakahori Y, Matsushita I, Abe T, Nagai R, Yazaki Y

机构信息

Department of Medicine III, University of Tokyo School of Medicine, Japan.

出版信息

Genomics. 1995 May 1;27(1):204-6. doi: 10.1006/geno.1995.1027.

DOI:10.1006/geno.1995.1027
PMID:7665173
Abstract

Homeobox-containing genes play critical roles in regulating tissue-specific gene expression essential for tissue differentiation, as well as determining the temporal and spatial patterns of development. Recently, a human cardiac homeobox-containing gene, CSX, has been isolated. CSX is abundantly expressed in the human heart from fetal stages, suggesting that CSX plays an important role in human heart formation. In the present study, we have determined the chromosomal localization of CSX by fluorescence in situ hybridization techniques and systemic screening of a yeast artificial chromosome library using polymerase chain reaction. By these methods, CSX was mapped to 5q34 of human chromosome 5 near the boundary of 5q34 and 5q35. In this region, another homeobox-containing gene MSX2, which is expressed in various tissues including the conduction system of the developing heart, has been assigned. Localization of CSX and MSX2 to the same region of the human chromosome suggests that these genes may be coordinately regulated during human heart formation.

摘要

含同源框的基因在调节组织特异性基因表达中发挥关键作用,这些基因表达对于组织分化至关重要,同时也决定了发育的时空模式。最近,一个含人类心脏同源框的基因CSX已被分离出来。CSX在胎儿期的人类心脏中大量表达,这表明CSX在人类心脏形成中发挥重要作用。在本研究中,我们通过荧光原位杂交技术以及使用聚合酶链反应对酵母人工染色体文库进行系统筛选,确定了CSX的染色体定位。通过这些方法,CSX被定位到人类5号染色体的5q34,靠近5q34和5q35的边界。在该区域,另一个含同源框的基因MSX2已被定位,MSX2在包括发育中心脏传导系统在内的各种组织中表达。CSX和MSX2定位于人类染色体的同一区域,这表明这些基因在人类心脏形成过程中可能受到协同调节。

相似文献

1
Assignment of cardiac homeobox gene CSX to human chromosome 5q34.心脏同源盒基因CSX定位于人类染色体5q34。
Genomics. 1995 May 1;27(1):204-6. doi: 10.1006/geno.1995.1027.
2
Csx: a murine homeobox-containing gene specifically expressed in the developing heart.Csx:一个在发育中的心脏中特异性表达的含小鼠同源异型盒基因。
Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8145-9. doi: 10.1073/pnas.90.17.8145.
3
Molecular cloning and characterization of human cardiac homeobox gene CSX1.人类心脏同源盒基因CSX1的分子克隆与特性分析
Circ Res. 1996 Nov;79(5):920-9. doi: 10.1161/01.res.79.5.920.
4
The cardiac homeobox gene Csx/Nkx2.5 lies genetically upstream of multiple genes essential for heart development.心脏同源盒基因Csx/Nkx2.5在基因层面上位于心脏发育所必需的多个基因的上游。
Development. 1999 Mar;126(6):1269-80. doi: 10.1242/dev.126.6.1269.
5
Molecular cloning, chromosomal mapping, and characterization of the human cardiac-specific homeobox gene hCsx.人类心脏特异性同源盒基因hCsx的分子克隆、染色体定位及特性分析
Mol Med. 1996 Jan;2(1):86-96.
6
Transcriptional regulation of human cardiac homeobox gene CSX1.人类心脏同源盒基因CSX1的转录调控
Biochem Biophys Res Commun. 2000 Jun 16;272(3):749-57. doi: 10.1006/bbrc.2000.2861.
7
Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand.心室特异性同源盒基因Irx4的心脏表达受Nkx2-5和dHand调控。
Dev Biol. 2000 Jan 15;217(2):266-77. doi: 10.1006/dbio.1999.9548.
8
Complex modular cis-acting elements regulate expression of the cardiac specifying homeobox gene Csx/Nkx2.5.复杂的模块化顺式作用元件调控心脏特异性同源盒基因Csx/Nkx2.5的表达。
Development. 1999 Apr;126(7):1439-50. doi: 10.1242/dev.126.7.1439.
9
Identification of the in vivo casein kinase II phosphorylation site within the homeodomain of the cardiac tisue-specifying homeobox gene product Csx/Nkx2.5.在心脏组织特异性同源盒基因产物Csx/Nkx2.5的同源结构域内鉴定体内酪蛋白激酶II磷酸化位点。
Mol Cell Biol. 1999 Jan;19(1):526-36. doi: 10.1128/MCB.19.1.526.
10
Ventricular noncompaction and distal chromosome 5q deletion.心室心肌致密化不全与5号染色体长臂远端缺失
Am J Med Genet. 1999 Aug 6;85(4):419-23.

引用本文的文献

1
Human Genetics of Truncus Arteriosus.动脉干畸形的人类遗传学。
Adv Exp Med Biol. 2024;1441:841-852. doi: 10.1007/978-3-031-44087-8_51.
2
Association between single-nucleotide polymorphisms of and congenital heart disease in Chinese population: A meta-analysis.中国人群中[具体基因]单核苷酸多态性与先天性心脏病的关联:一项荟萃分析。 (注:原文中“of ”部分缺失具体基因名称)
Open Life Sci. 2022 May 12;17(1):473-482. doi: 10.1515/biol-2022-0058. eCollection 2022.
3
Developmental retardation due to paternal 5q/11q translocation in a Chinese infant: clinical, chromosomal and microarray characterization.
一名中国婴儿因父源性5号染色体长臂/11号染色体长臂易位导致发育迟缓:临床、染色体及微阵列特征分析
J Genet. 2019 Sep;98.
4
Analysis of NKX2-5 in 439 Chinese Patients with Sporadic Atrial Septal Defect.分析 439 例散发性房间隔缺损患者的 NKX2-5。
Med Sci Monit. 2019 Apr 15;25:2756-2763. doi: 10.12659/MSM.916052.
5
Novel Point Mutations in the Gene in Pediatric Patients with Non-Familial Congenital Heart Disease.在非家族性先天性心脏病的儿科患者中,基因的新突变。
Medicina (Kaunas). 2018 Jun 19;54(3):46. doi: 10.3390/medicina54030046.
6
Electrical disorders in atrial septal defect: genetics and heritability.房间隔缺损中的电学紊乱:遗传学与遗传度
J Thorac Dis. 2018 Sep;10(Suppl 24):S2848-S2853. doi: 10.21037/jtd.2018.02.53.
7
Computational modeling suggests impaired interactions between NKX2.5 and GATA4 in individuals carrying a novel pathogenic D16N NKX2.5 mutation.计算模型表明,携带新型致病性D16N NKX2.5突变的个体中,NKX2.5与GATA4之间的相互作用受损。
Oncotarget. 2018 Feb 9;9(17):13713-13732. doi: 10.18632/oncotarget.24459. eCollection 2018 Mar 2.
8
Genome-wide analysis reveals conserved transcriptional responses downstream of resting potential change in Xenopus embryos, axolotl regeneration, and human mesenchymal cell differentiation.全基因组分析揭示了非洲爪蟾胚胎、蝾螈再生及人间充质细胞分化过程中静息电位变化下游保守的转录反应。
Regeneration (Oxf). 2015 Nov 26;3(1):3-25. doi: 10.1002/reg2.48. eCollection 2016 Feb.
9
Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.NKX2-5 基因在孤立性心房颤动患者中的突变谱。
Int J Med Sci. 2014 Apr 7;11(6):554-63. doi: 10.7150/ijms.8407. eCollection 2014.
10
A case report of truncus arteriosus communis and genetic counseling.共同动脉干病例报告及遗传咨询
ARYA Atheroscler. 2013 Jun;9(4):254-9.