• 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

Construction and characterization of a highly stable human: rodent monochromosomal hybrid panel for genetic complementation and genome mapping studies.

作者信息

Cuthbert A P, Trott D A, Ekong R M, Jezzard S, England N L, Themis M, Todd C M, Newbold R F

机构信息

Department of Biology and Biochemistry, Brunel University, Uxbridge, UK.

出版信息

Cytogenet Cell Genet. 1995;71(1):68-76. doi: 10.1159/000134066.

DOI:10.1159/000134066
PMID:7606932
Abstract

Human:rodent somatic cell hybrids carrying a single, intact, selectable human chromosome are valuable both for functional somatic cell genetic analysis and genome mapping procedures. Here, we describe the construction and detailed molecular cytogenetic characterization of a panel of 23 stable hybrids, representing all 22 human autosomes plus the X-chromosome. Individual normal human chromosomes have been tagged with a selectable fusion gene (Hytk) introduced into the chromosome in a small (4.2 kbp) retroviral vector. Use of the Hytk marker permits both positive and negative ("in-out") selection to be applied to the human chromosome in any mammalian cell background. The panel includes 18 new hybrids isolated by direct microcell transfer from normal human diploid fibroblasts into mouse A9 cells.

摘要

相似文献

1
Construction and characterization of a highly stable human: rodent monochromosomal hybrid panel for genetic complementation and genome mapping studies.
Cytogenet Cell Genet. 1995;71(1):68-76. doi: 10.1159/000134066.
2
Construction and analysis of microcell hybrids containing dual selectable tagged human chromosomes.含有双选择标记人类染色体的微细胞杂种的构建与分析。
Cytogenet Cell Genet. 1995;69(1-2):63-5. doi: 10.1159/000133939.
3
Integration of a dominant selectable marker into human chromosomes and transfer of marked chromosomes to mouse cells by microcell fusion.将显性选择标记整合到人类染色体中,并通过微细胞融合将标记的染色体转移到小鼠细胞中。
Somat Cell Mol Genet. 1985 Mar;11(2):177-87. doi: 10.1007/BF01534706.
4
A method for constructing radiation hybrid maps of whole genomes.一种构建全基因组辐射杂种图谱的方法。
Nat Genet. 1994 May;7(1):22-8. doi: 10.1038/ng0594-22.
5
Monochromosomal rodent-human hybrids from microcell fusion of human lymphoblastoid cells containing an inserted dominant selectable marker.
Genomics. 1990 Feb;6(2):358-66. doi: 10.1016/0888-7543(90)90577-h.
6
Construction of microcell hybrid clones containing specific mouse chromosomes: application to autosomes 8 and 17.包含特定小鼠染色体的微细胞杂交克隆的构建:应用于常染色体8和17
Mol Cell Biol. 1982 May;2(5):526-34. doi: 10.1128/mcb.2.5.526-534.1982.
7
Regional localization of 188 sequence tagged sites on a somatic cell hybrid mapping panel for human chromosome 3.
Genomics. 1994 Dec;24(3):549-56. doi: 10.1006/geno.1994.1665.
8
Mapping a novel cellular-senescence gene to human chromosome 2q37 by irradiation microcell-mediated chromosome transfer.通过辐射微细胞介导的染色体转移将一个新的细胞衰老基因定位于人类染色体2q37。
Mol Carcinog. 1998 May;22(1):34-45. doi: 10.1002/(sici)1098-2744(199805)22:1<34::aid-mc5>3.0.co;2-l.
9
Mouse A9 cells containing single human chromosomes for analysis of genomic imprinting.含有单条人类染色体的小鼠A9细胞用于基因组印记分析。
DNA Res. 1999 Jun 30;6(3):165-72. doi: 10.1093/dnares/6.3.165.
10
Construction of 700 human/mouse A9 monochromosomal hybrids and analysis of imprinted genes on human chromosome 6.构建700个人类/小鼠A9单染色体杂种并分析人类6号染色体上的印记基因。
J Hum Genet. 2001;46(3):137-45. doi: 10.1007/s100380170101.

引用本文的文献

1
Human NORs, comprising rDNA arrays and functionally conserved distal elements, are located within dynamic chromosomal regions.人类 NORs 包含 rDNA 阵列和功能保守的远端元件,位于动态染色体区域内。
Genes Dev. 2019 Dec 1;33(23-24):1688-1701. doi: 10.1101/gad.331892.119. Epub 2019 Nov 14.
2
Functional role of and candidate genes on the regulation of gene expression.和候选基因在基因表达调控中的功能作用。 (原文中“and”前后内容缺失,可能影响准确理解,以上是按现有内容翻译)
Oncotarget. 2017 Jun 27;8(37):61890-61900. doi: 10.18632/oncotarget.18712. eCollection 2017 Sep 22.
3
Monochromosomal Hybrids and Chromosome Transfer: A Functional Approach for Gene Identification.
单染色体杂种与染色体转移:一种用于基因鉴定的功能方法。
Cancer Genomics Proteomics. 2017 Mar-Apr;14(2):93-101. doi: 10.21873/cgp.20022.
4
Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism.ABCD4 基因突变导致一种新的维生素 B12 代谢先天性错误。
Nat Genet. 2012 Oct;44(10):1152-5. doi: 10.1038/ng.2386. Epub 2012 Aug 26.
5
Mutations in C12orf62, a factor that couples COX I synthesis with cytochrome c oxidase assembly, cause fatal neonatal lactic acidosis.C12orf62 中的突变会导致 COX I 合成与细胞色素 c 氧化酶组装偶联,从而引起致命的新生儿乳酸酸中毒。
Am J Hum Genet. 2012 Jan 13;90(1):142-51. doi: 10.1016/j.ajhg.2011.11.027.
6
Microcell-mediated chromosome transfer identifies EPB41L3 as a functional suppressor of epithelial ovarian cancers.微细胞介导的染色体转移鉴定出 EPB41L3 是上皮性卵巢癌的功能性抑制因子。
Neoplasia. 2010 Jul;12(7):579-89. doi: 10.1593/neo.10340.
7
LMBRD1: the gene for the cblF defect of vitamin B₁₂ metabolism.LMBRD1:钴胺素代谢 cblF 缺陷的基因。
J Inherit Metab Dis. 2011 Feb;34(1):121-6. doi: 10.1007/s10545-010-9083-9. Epub 2010 May 6.
8
Insights into lysosomal cobalamin trafficking: lessons learned from cblF disease.溶酶体钴胺素转运的研究进展:cblF 病的启示。
J Mol Med (Berl). 2010 May;88(5):459-66. doi: 10.1007/s00109-010-0601-x. Epub 2010 Feb 20.
9
Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome.编码细胞色素c氧化酶I翻译激活因子的TACO1发生突变,会导致细胞色素c氧化酶缺乏症和迟发性 Leigh 综合征。
Nat Genet. 2009 Jul;41(7):833-7. doi: 10.1038/ng.390. Epub 2009 Jun 7.
10
Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism.在维生素B12代谢的cblF缺陷中改变的一种假定溶酶体钴胺素转运蛋白的鉴定。
Nat Genet. 2009 Feb;41(2):234-9. doi: 10.1038/ng.294. Epub 2009 Jan 11.