• 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

编码磷酸核糖甘氨酰胺甲酰基转移酶的基因定位于人类第14号染色体。

Assignment of the gene coding for phosphoribosylglycineamide formyltransferase to human chromosome 14.

作者信息

Jones C, Patterson D, Kao F T

出版信息

Somatic Cell Genet. 1981 Jul;7(4):399-409. doi: 10.1007/BF01542985.

DOI:10.1007/BF01542985
PMID:7197058
Abstract

Purine-requiring Chinese hamster ovary cell auxotrophs of the complementation class ade-E were hybridized with various human cells, and hybrids were isolated under selective conditions in which the retention of the complementing gene on the human chromosome is necessary for survival. Synteny analysis in 72 primary and secondary hybrid clones using isozyme, karyotypic, and biochemical methods provides evidence for an assignment of the gene for phosphoribosylglycineamide formyltransferase (GART, EC 2.1.2.2), deficient in ade-E mutants, to human chromosome 14. The importance of this gene assignment to the development of hypotheses regarding the organization, structure, and regulation of genes involved in the same biosynthetic pathway in mammalian cells is discussed.

摘要

将互补类 ade - E 的需要嘌呤的中国仓鼠卵巢细胞营养缺陷型与各种人类细胞杂交,并在选择性条件下分离杂种细胞,在这些条件下,人类染色体上互补基因的保留对细胞存活是必需的。使用同工酶、核型和生化方法对 72 个初级和次级杂种克隆进行同线分析,为将 ade - E 突变体中缺乏的磷酸核糖甘氨酰胺甲酰基转移酶(GART,EC 2.1.2.2)基因定位于人类 14 号染色体提供了证据。讨论了这一基因定位对于形成关于哺乳动物细胞中参与同一生物合成途径的基因的组织、结构和调控的假说的重要性。

相似文献

1
Assignment of the gene coding for phosphoribosylglycineamide formyltransferase to human chromosome 14.编码磷酸核糖甘氨酰胺甲酰基转移酶的基因定位于人类第14号染色体。
Somatic Cell Genet. 1981 Jul;7(4):399-409. doi: 10.1007/BF01542985.
2
Expression of a human cDNA encoding a protein containing GAR synthetase, AIR synthetase, and GAR transformylase corrects the defects in mutant Chinese hamster ovary cells lacking these activities.编码一种包含甘氨酰胺核糖核苷酸(GAR)合成酶、5-氨基咪唑核糖核苷酸(AIR)合成酶和GAR转甲酰基酶的蛋白质的人互补DNA(cDNA)的表达可纠正缺乏这些活性的突变型中国仓鼠卵巢细胞中的缺陷。
Somat Cell Mol Genet. 1991 Jul;17(4):411-20. doi: 10.1007/BF01233066.
3
Assignment of a third purine biosynthetic gene (glycinamide ribonucleotide transformylase) to human chromosome 21.将第三个嘌呤生物合成基因(甘氨酰胺核糖核苷酸转甲酰基酶)定位于人类21号染色体。
Am J Hum Genet. 1986 Aug;39(2):179-85.
4
Cloning and in vivo expression of the human GART gene using yeast artificial chromosomes.利用酵母人工染色体克隆和体内表达人类GART基因。
EMBO J. 1991 Jul;10(7):1629-34. doi: 10.1002/j.1460-2075.1991.tb07685.x.
5
Demonstration, by somatic cell genetics, of coordinate regulation of genes for two enzymes of purine synthesis assigned to human chromosome 21.通过体细胞遗传学证明,定位于人类21号染色体上的嘌呤合成途径中两种酶的基因存在协同调控。
Proc Natl Acad Sci U S A. 1981 Jan;78(1):405-9. doi: 10.1073/pnas.78.1.405.
6
New gene assignments using a complete, characterized sheep-hamster somatic cell hybrid panel.利用一个完整的、经过特征鉴定的绵羊 - 仓鼠体细胞杂交细胞系进行新基因定位。
Anim Genet. 1998 Feb;29(1):48-54. doi: 10.1046/j.1365-2052.1998.00253.x.
7
Association of human chromosome 14 with a ts defect in G1 of Chinese hamster K12 cells.
Cell Biol Int Rep. 1979 Mar;3(2):169-78. doi: 10.1016/0309-1651(79)90123-1.
8
Cloning of three human multifunctional de novo purine biosynthetic genes by functional complementation of yeast mutations.通过酵母突变体的功能互补克隆三个人类多功能从头嘌呤生物合成基因。
Proc Natl Acad Sci U S A. 1990 Apr;87(8):2916-20. doi: 10.1073/pnas.87.8.2916.
9
GART, SON, IFNAR, and CRF2-4 genes cluster on human chromosome 21 and mouse chromosome 16.GART、SON、IFNAR和CRF2 - 4基因聚集在人类21号染色体和小鼠16号染色体上。
Mamm Genome. 1993;4(6):338-42. doi: 10.1007/BF00357094.
10
Transfer of the human HPRT and GART genes from yeast to mammalian cells by microinjection of YAC DNA.通过显微注射酵母人工染色体(YAC)DNA将人类次黄嘌呤磷酸核糖转移酶(HPRT)基因和甘氨酰胺核糖核苷酸转甲酰基酶(GART)基因从酵母转移至哺乳动物细胞。
Somat Cell Mol Genet. 1991 Nov;17(6):573-80. doi: 10.1007/BF01233622.

引用本文的文献

1
Cloning, sequencing, and analysis of inv8 chromosome breakpoints associated with recombinant 8 syndrome.与重组8综合征相关的inv8染色体断点的克隆、测序及分析
Am J Hum Genet. 2000 Mar;66(3):1138-44. doi: 10.1086/302821.
2
Assignment of the structural gene coding for albumin to human chromosome 4.将编码白蛋白的结构基因定位于人类第4号染色体。
Hum Genet. 1982;62(4):337-41. doi: 10.1007/BF00304551.
3
Isolation and chromosomal localization of unique DNA sequences from a human genomic library.从人类基因组文库中分离独特DNA序列并进行染色体定位。
Proc Natl Acad Sci U S A. 1982 Feb;79(3):865-9. doi: 10.1073/pnas.79.3.865.
4
Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells.人类c-myc癌基因位于8号染色体上,该区域在伯基特淋巴瘤细胞中发生易位。
Proc Natl Acad Sci U S A. 1982 Dec;79(24):7824-7. doi: 10.1073/pnas.79.24.7824.
5
Human ferritin gene is assigned to chromosome 19.人类铁蛋白基因定位于第19号染色体。
Proc Natl Acad Sci U S A. 1983 Jan;80(2):482-6. doi: 10.1073/pnas.80.2.482.
6
Assignment of first random restriction fragment length polymorphism (RFLP) locus ((D14S1) to a region of human chromosome 14.将首个随机限制性片段长度多态性(RFLP)位点(D14S1)定位到人类14号染色体的一个区域。
Am J Hum Genet. 1982 Mar;34(2):216-26.
7
Selective transfer of individual human chromosomes to recipient cells.将人类个体染色体选择性转移至受体细胞。
Mol Cell Biol. 1985 Jan;5(1):140-6. doi: 10.1128/mcb.5.1.140-146.1985.
8
Assignment of a third purine biosynthetic gene (glycinamide ribonucleotide transformylase) to human chromosome 21.将第三个嘌呤生物合成基因(甘氨酰胺核糖核苷酸转甲酰基酶)定位于人类21号染色体。
Am J Hum Genet. 1986 Aug;39(2):179-85.
9
Multiple purine pathway enzyme activities are encoded at a single genetic locus in Drosophila.果蝇中多个嘌呤代谢途径酶的活性由单个基因位点编码。
Proc Natl Acad Sci U S A. 1986 Feb;83(3):720-4. doi: 10.1073/pnas.83.3.720.
10
Papillomavirus sequences integrate near cellular oncogenes in some cervical carcinomas.在一些宫颈癌中,乳头瘤病毒序列整合在细胞癌基因附近。
Proc Natl Acad Sci U S A. 1987 Feb;84(4):1070-4. doi: 10.1073/pnas.84.4.1070.