• 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

从一个经流式细胞分选的人类8号染色体文库中分离并鉴定出可检测限制性片段长度多态性(RFLP)的DNA探针。

Isolation and characterization of DNA probes from a flow-sorted human chromosome 8 library that detect restriction fragment length polymorphism (RFLP).

作者信息

Wood S, Starr T V, Shukin R J

出版信息

Am J Hum Genet. 1986 Dec;39(6):744-50.

PMID:2879441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1684124/
Abstract

We have used a recombinant DNA library constructed from flow-sorted human chromosome 8 as a source of single-copy human probes. These probes have been screened for restriction fragment length polymorphism (RFLP) by hybridization to Southern transfers of genomic DNA from five unrelated individuals. We have detected six RFLPs distributed among four probes after screening 741 base pairs for restriction site variation. These RFLPs all behave as codominant Mendelian alleles. Two of the probes detect rare variants, while the other two detect RFLPs with PIC values of .36 and .16. Informative probes will be useful for the construction of a linkage map for chromosome 8 and for the localization of mutant alleles to this chromosome.

摘要

我们使用了一个由流式分选的人类8号染色体构建的重组DNA文库作为单拷贝人类探针的来源。通过与来自五个无关个体的基因组DNA的Southern印迹杂交,对这些探针进行了限制性片段长度多态性(RFLP)筛选。在筛选741个碱基对的限制性位点变异后,我们在四个探针中检测到六个RFLP。这些RFLP均表现为共显性孟德尔等位基因。其中两个探针检测到罕见变异,而另外两个探针检测到PIC值分别为0.36和0.16的RFLP。信息丰富的探针将有助于构建8号染色体的连锁图谱,并将突变等位基因定位到该染色体上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d69/1684124/10e3a5d9dbf8/ajhg00148-0071-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d69/1684124/10e3a5d9dbf8/ajhg00148-0071-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d69/1684124/10e3a5d9dbf8/ajhg00148-0071-a.jpg

相似文献

1
Isolation and characterization of DNA probes from a flow-sorted human chromosome 8 library that detect restriction fragment length polymorphism (RFLP).从一个经流式细胞分选的人类8号染色体文库中分离并鉴定出可检测限制性片段长度多态性(RFLP)的DNA探针。
Am J Hum Genet. 1986 Dec;39(6):744-50.
2
Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p.16号染色体富集噬菌体文库的构建及16p若干DNA片段的特征分析
Hum Genet. 1987 Oct;77(2):95-103. doi: 10.1007/BF00272372.
3
Isolation of polymorphic DNA segments from human chromosome 21.从人类21号染色体中分离多态性DNA片段。
Nucleic Acids Res. 1985 Sep 11;13(17):6075-88. doi: 10.1093/nar/13.17.6075.
4
Isolation of polymorphic DNA fragments from human chromosome 4.从人类4号染色体中分离多态性DNA片段。
Nucleic Acids Res. 1987 Feb 25;15(4):1445-58. doi: 10.1093/nar/15.4.1445.
5
The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies.人纤连蛋白受体β亚基基因座:DNA限制性片段长度多态性及连锁图谱研究。
Hum Genet. 1989 Nov;83(4):383-90. doi: 10.1007/BF00291386.
6
Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.从人类13号染色体中分离并对揭示多态性位点的DNA片段进行区域定位。
Am J Hum Genet. 1984 Jan;36(1):10-24.
7
Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genes.对大量(2000个)人类3号染色体上的单拷贝DNA片段进行分离和区域定位,用于绘制和克隆肿瘤抑制基因图谱。
Hum Genet. 1991 Apr;86(6):567-77. doi: 10.1007/BF00201543.
8
Pst I restriction fragment length polymorphism of human placental alkaline phosphatase gene: Mendelian segregation and localization of mutation site in the gene.人胎盘碱性磷酸酶基因的Pst I限制性片段长度多态性:孟德尔分离及基因突变位点的定位
Proc Natl Acad Sci U S A. 1988 Oct;85(20):7680-4. doi: 10.1073/pnas.85.20.7680.
9
Identification and characterization of 23 RFLP loci by screening random cosmid genomic clones.通过筛选随机黏粒基因组克隆鉴定并表征23个限制性片段长度多态性(RFLP)位点。
Am J Hum Genet. 1989 May;44(5):671-8.
10
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.

引用本文的文献

1
D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p).D8S7在8号染色体短臂的反向重复(inv dup 8p)中持续缺失。
Hum Genet. 1993 Oct;92(4):391-6. doi: 10.1007/BF01247342.
2
Chromosomal localization of the human proenkephalin and prodynorphin genes.人类前脑啡肽原和前强啡肽基因的染色体定位。
Am J Hum Genet. 1988 Feb;42(2):327-34.
3
Physical mapping of D8S7 and D8S11 to the band 8p23.1 of the short arm of chromosome 8.将D8S7和D8S11定位到8号染色体短臂的8p23.1带。

本文引用的文献

1
A polymorphic DNA marker genetically linked to Huntington's disease.一种与亨廷顿舞蹈症基因连锁的多态性DNA标记。
Nature. 1983;306(5940):234-8. doi: 10.1038/306234a0.
2
Strategies for detecting and characterizing restriction fragment length polymorphisms (RFLP's).检测和鉴定限制性片段长度多态性(RFLP)的策略。
Cytogenet Cell Genet. 1982;32(1-4):58-67. doi: 10.1159/000131687.
3
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.利用限制性片段长度多态性构建人类遗传连锁图谱。
Nucleic Acids Res. 1989 Oct 25;17(20):8395. doi: 10.1093/nar/17.20.8395.
4
Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma.杂合性缺失提示存在与原发性肝细胞癌相关的肿瘤抑制基因。
Proc Natl Acad Sci U S A. 1989 Nov;86(22):8852-6. doi: 10.1073/pnas.86.22.8852.
5
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates.一份详细的人类4号染色体多点图谱为连锁异质性和位置特异性重组率提供了证据。
Am J Hum Genet. 1991 May;48(5):911-25.
Am J Hum Genet. 1980 May;32(3):314-31.
4
Restriction sites containing CpG show a higher frequency of polymorphism in human DNA.含有CpG的限制性酶切位点在人类DNA中显示出更高的多态性频率。
Cell. 1984 Jan;36(1):131-8. doi: 10.1016/0092-8674(84)90081-3.
5
A closely linked genetic marker for cystic fibrosis.一种与囊性纤维化紧密连锁的遗传标记。
Nature. 1985;318(6044):382-4. doi: 10.1038/318382a0.
6
Report of the Committee on the Genetic Constitution of Chromosomes 7, 8 and 9.
Cytogenet Cell Genet. 1985;40(1-4):156-78. doi: 10.1159/000132173.
7
A DNA marker for human chromosome 8 that detects alleles of differing sizes.
Cytogenet Cell Genet. 1986;42(3):113-8. doi: 10.1159/000132262.
8
Localization of cystic fibrosis locus to human chromosome 7cen-q22.囊性纤维化基因座定位于人类染色体7cen-q22。
Nature. 1985;318(6044):384-5. doi: 10.1038/318384a0.
9
Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker.由基因连锁多态性DNA标记物定义的囊性纤维化位点。
Science. 1985 Nov 29;230(4729):1054-7. doi: 10.1126/science.2997931.
10
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs.利用紧密连锁的限制性片段长度多态性进行杜氏肌营养不良症的产前诊断和携带者检测。
Lancet. 1985 Mar 23;1(8430):655-8. doi: 10.1016/s0140-6736(85)91325-x.