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通过场反转凝胶电泳对人绒毛膜促性腺激素β亚基基因进行黏粒图谱分析。

Cosmid mapping of the human chorionic gonadotropin beta subunit genes by field-inversion gel electrophoresis.

作者信息

Graham M Y, Otani T, Boime I, Olson M V, Carle G F, Chaplin D D

出版信息

Nucleic Acids Res. 1987 Jun 11;15(11):4437-48. doi: 10.1093/nar/15.11.4437.

DOI:10.1093/nar/15.11.4437
PMID:3035494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC340872/
Abstract

A cosmid clone containing the entire hCG beta gene cluster has been isolated. The restriction map of this clone has been determined by an indirect-end-label FIGE (field inversion gel electrophoresis) method. Analysis of this cosmid clone shows that there are 6 hCG beta genes in human genomic DNA. A previously uncloned portion of the hCG beta cluster, termed the "gap" region, has been shown not to contain any sequences homologous to the hCG beta cDNA. The restriction mapping method employed in this study takes advantage of the superior resolution of FIGE for high molecular weight DNA fragments in the size range 15-50 kb. This method is broadly applicable and permits rapid and accurate restriction mapping for extended regions of genomic DNA that have been cloned into cosmid or lambda vectors.

摘要

一个包含完整人绒毛膜促性腺激素β基因簇的黏粒克隆已被分离出来。该克隆的限制性图谱已通过间接末端标记场反转凝胶电泳(FIGE)方法确定。对这个黏粒克隆的分析表明,人类基因组DNA中有6个人绒毛膜促性腺激素β基因。人绒毛膜促性腺激素β基因簇中一个以前未克隆的部分,称为“缺口”区域,已被证明不包含与人绒毛膜促性腺激素β互补DNA同源的任何序列。本研究中使用的限制性图谱绘制方法利用了FIGE对大小在15 - 50 kb范围内的高分子量DNA片段的卓越分辨率。该方法具有广泛的适用性,可对已克隆到黏粒或λ载体中的基因组DNA扩展区域进行快速准确的限制性图谱绘制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/340872/4e3e38213925/nar00255-0088-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/340872/bcb06d135b1f/nar00255-0083-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/340872/f4a643b7776c/nar00255-0085-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/340872/4e3e38213925/nar00255-0088-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/340872/bcb06d135b1f/nar00255-0083-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/340872/f4a643b7776c/nar00255-0085-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/340872/4e3e38213925/nar00255-0088-a.jpg

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Cosmid mapping of the human chorionic gonadotropin beta subunit genes by field-inversion gel electrophoresis.通过场反转凝胶电泳对人绒毛膜促性腺激素β亚基基因进行黏粒图谱分析。
Nucleic Acids Res. 1987 Jun 11;15(11):4437-48. doi: 10.1093/nar/15.11.4437.
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Studies on locus expansion, library representation, and chromosome walking using an efficient method to screen cosmid libraries.利用一种高效方法筛选黏粒文库进行基因座扩增、文库表征及染色体步移的研究。
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Recovery of DNA from gels.从凝胶中回收DNA。
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Molecular map of the murine S region.小鼠S区域的分子图谱。
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Isolation and characterization of the human chorionic gonadotropin beta subunit (CG beta) gene cluster: regulation of transcriptionally active CG beta gene by cyclic AMP.人绒毛膜促性腺激素β亚基(CGβ)基因簇的分离与鉴定:环磷酸腺苷对转录活性CGβ基因的调控
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Molecular evidence that the H-2D and H-2L genes arose by duplication. Differences between the evolution of the class I genes in mice and humans.H-2D和H-2L基因通过复制产生的分子证据。小鼠和人类I类基因进化的差异。
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The basis of high resolution separation of small DNAs by asymmetric-voltage field inversion electrophoresis and its application to DNA sequencing gels.非对称电压场反转电泳用于小DNA高分辨率分离的基础及其在DNA测序凝胶中的应用
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Field inversion gel electrophoresis with different pulse time ramps.具有不同脉冲时间梯度的场反转凝胶电泳。
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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。
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The danger of studying human chorionic gonadotrophin action or expression in animal models.在动物模型中研究人绒毛膜促性腺激素作用或表达的风险。
Br J Cancer. 1991 May;63(5):827. doi: 10.1038/bjc.1991.184.
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The construction of cosmid libraries which can be used to transform eukaryotic cells.可用于转化真核细胞的黏粒文库的构建。
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The gene encoding the common alpha subunit of the four human glycoprotein hormones.编码四种人类糖蛋白激素共同α亚基的基因。
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Rapid and efficient cosmid cloning.快速高效的黏粒克隆
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Glycoprotein hormones: structure and function.糖蛋白激素:结构与功能
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Only three of the seven human chorionic gonadotropin beta subunit genes can be expressed in the placenta.在人绒毛膜促性腺激素β亚基的七个基因中,只有三个基因能在胎盘中表达。
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10
The beta subunit of human chorionic gonadotropin is encoded by multiple genes.人绒毛膜促性腺激素的β亚基由多个基因编码。
J Biol Chem. 1983 Oct 10;258(19):11492-9.