• 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

人腺嘌呤磷酸核糖转移酶基因(APRT)位于触珠蛋白(HP)和16号染色体脆性位点(fra(16)(q23),即FRA16D)位点远端的一个新位置。

A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23)(FRA16D) loci.

作者信息

Fratini A, Simmers R N, Callen D F, Hyland V J, Tischfield J A, Stambrook P J, Sutherland G R

出版信息

Cytogenet Cell Genet. 1986;43(1-2):10-3. doi: 10.1159/000132291.

DOI:10.1159/000132291
PMID:3780312
Abstract

The human adenine phosphoribosyltransferase gene (APRT) was mapped with respect to the haptoglobin gene (HP) and the fragile site at 16q23.2 (FRA16D). A subclone of APRT and a cDNA clone of HP were used for molecular hybridization to DNA from mouse-human hybrid cell lines containing specific chromosome 16 translocations. The APRT subclone was used for in situ hybridization to chromosomes expressing FRA16D. APRT was found to be distal to HP and FRA16D and was localized at 16q24, making the gene order cen-FRA16B-HP-FRA16D-APRT-qter.

摘要

人类腺嘌呤磷酸核糖转移酶基因(APRT)相对于触珠蛋白基因(HP)和位于16q23.2的脆性位点(FRA16D)进行了定位。APRT的一个亚克隆和HP的一个cDNA克隆用于与来自含有特定16号染色体易位的小鼠-人杂交细胞系的DNA进行分子杂交。APRT亚克隆用于对表达FRA16D的染色体进行原位杂交。发现APRT位于HP和FRA16D的远端,定位于16q24,基因顺序为cen-FRA16B-HP-FRA16D-APRT-qter。

相似文献

1
A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23)(FRA16D) loci.人腺嘌呤磷酸核糖转移酶基因(APRT)位于触珠蛋白(HP)和16号染色体脆性位点(fra(16)(q23),即FRA16D)位点远端的一个新位置。
Cytogenet Cell Genet. 1986;43(1-2):10-3. doi: 10.1159/000132291.
2
Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16.将基因探针和无名DNA片段精细定位到16号染色体长臂上。
Genomics. 1988 Feb;2(2):144-53. doi: 10.1016/0888-7543(88)90096-1.
3
Localization of the human haptoglobin genes distal to the fragile site at 16q22 using in situ hybridization.
Cytogenet Cell Genet. 1986;41(1):38-41. doi: 10.1159/000132193.
4
High-frequency structural gene deletion as the basis for functional hemizygosity of the adenine phosphoribosyltransferase locus in Chinese hamster ovary cells.高频结构基因缺失作为中国仓鼠卵巢细胞中腺嘌呤磷酸核糖转移酶基因座功能半合子状态的基础。
Proc Natl Acad Sci U S A. 1983 Oct;80(19):5961-4. doi: 10.1073/pnas.80.19.5961.
5
Assignment of the gene for adenine phosphoribosyltransferase on the genetic map of mouse chromosome 8.腺嘌呤磷酸核糖转移酶基因在小鼠8号染色体遗传图谱上的定位
Biochem Genet. 1987 Aug;25(7-8):563-8. doi: 10.1007/BF00554357.
6
Cloning the complete human adenine phosphoribosyl transferase gene.克隆完整的人类腺嘌呤磷酸核糖转移酶基因。
Gene. 1984 Nov;31(1-3):233-40. doi: 10.1016/0378-1119(84)90214-2.
7
Cloning of a Drosophila melanogaster adenine phosphoribosyltransferase structural gene and deduced amino acid sequence of the enzyme.果蝇腺嘌呤磷酸核糖转移酶结构基因的克隆及该酶推导的氨基酸序列
Gene. 1987;59(1):77-86. doi: 10.1016/0378-1119(87)90268-x.
8
Assignment of a processed mouse Aprt pseudogene to the same chromosome as the functional gene.将一个经过加工的小鼠Aprt假基因定位到与功能基因相同的染色体上。
Cytogenet Cell Genet. 1986;42(4):198-201. doi: 10.1159/000132278.
9
Expression of recessive Aprt- mutations in mouse CAK cells resulting from chromosome loss and duplication.染色体丢失和重复导致小鼠CAK细胞中隐性Aprt-突变的表达。
Somatic Cell Genet. 1983 Nov;9(6):771-8. doi: 10.1007/BF01539479.
10
Preferential loss or inactivation of chromosome Z4 APRT allele in CHO cells.中国仓鼠卵巢细胞中Z4 APRT染色体等位基因的优先丢失或失活。
Somat Cell Mol Genet. 1989 Jul;15(4):271-7. doi: 10.1007/BF01534966.

引用本文的文献

1
Are common fragile sites merely structural domains or highly organized "functional" units susceptible to oncogenic stress?常见脆性位点仅仅是结构域还是易受致癌应激影响的高度组织化的“功能”单元?
Cell Mol Life Sci. 2014 Dec;71(23):4519-44. doi: 10.1007/s00018-014-1717-x. Epub 2014 Sep 20.
2
Comparison between various strategies for the disease-gene mapping using linkage disequilibrium analyses: studies on adenine phosphoribosyltransferase deficiency used as an example.使用连锁不平衡分析进行疾病基因定位的各种策略之间的比较:以腺嘌呤磷酸核糖转移酶缺乏症研究为例
J Hum Genet. 2004;49(9):463-473. doi: 10.1007/s10038-004-0175-y. Epub 2004 Jul 28.
3
Chromosomal assignment of seven genes on canine chromosomes by fluorescence in situ hybridization.
Mamm Genome. 1996 Apr;7(4):268-70. doi: 10.1007/s003359900080.
4
Adenine phosphoribosyltransferase-deficient mice develop 2,8-dihydroxyadenine nephrolithiasis.腺嘌呤磷酸核糖转移酶缺陷型小鼠会患上2,8 - 二羟基腺嘌呤肾结石病。
Proc Natl Acad Sci U S A. 1996 May 28;93(11):5307-12. doi: 10.1073/pnas.93.11.5307.
5
Comparative anatomy of the human APRT gene and enzyme: nucleotide sequence divergence and conservation of a nonrandom CpG dinucleotide arrangement.人类APRT基因与酶的比较解剖学:核苷酸序列差异以及非随机CpG二核苷酸排列的保守性
Proc Natl Acad Sci U S A. 1987 May;84(10):3349-53. doi: 10.1073/pnas.84.10.3349.
6
Anonymous DNA probes to human chromosome 16 derived from a flow-purified library.源自流式纯化文库的人16号染色体匿名DNA探针。
Am J Hum Genet. 1988 Feb;42(2):373-9.
7
A fragile site in the human U2 small nuclear RNA gene cluster is revealed by adenovirus type 12 infection.12型腺病毒感染揭示了人类U2小核RNA基因簇中的一个易碎位点。
Mol Cell Biol. 1988 May;8(5):1863-7. doi: 10.1128/mcb.8.5.1863-1867.1988.
8
Restriction fragment length polymorphisms detected by anonymous DNA probes mapped to defined intervals of human chromosome 16.通过匿名DNA探针检测到的限制性片段长度多态性定位于人类16号染色体的特定区间。
Hum Genet. 1988 Jul;79(3):277-9. doi: 10.1007/BF00366251.
9
Sph I restriction fragment length polymorphism on human chromosome 16 detected with an APRT gene probe.用一个APRT基因探针检测人类16号染色体上的Sph I限制性片段长度多态性。
Nucleic Acids Res. 1987 Nov 25;15(22):9615. doi: 10.1093/nar/15.22.9615.
10
Genetic linkage map of 46 DNA markers on human chromosome 16.人类16号染色体上46个DNA标记的遗传连锁图谱。
Proc Natl Acad Sci U S A. 1990 Aug;87(15):5754-8. doi: 10.1073/pnas.87.15.5754.