LOCALIZATION OF THE XANTHINE GUANINE PHOSPHORIBOSYL TRANSFERASE GENE (GPT) OF ESCHERICHIA-COLI IN AS52 METAPHASE CELLS BY FLUORESCENCE IN-SITU HYBRIDIZATION

被引:0
|
作者
MICHAELIS, KC
HELVERING, LM
KINDIG, DE
GARRIOTT, ML
RICHARDSON, KK
机构
[1] Toxicology Research Laboratories, Lilly Research Laboratories, A Division of Eli Lilly and Company, Greenfield, Indiana
关键词
DIGOXIGENIN; IMMUNOFLUORESCENT; FITC; POLYMERASE CHAIN REACTION (PCR);
D O I
10.1002/em.2850240306
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The purpose of this study was to localize the xanthine guanine phosphoribosyl transferase gene (gpt) to a specific chromosome to investigate its proposed autosomal location in the AS52 cell line. AS52 cells are hgprt-deficient Chinese hamster ovary (CHO) cells which carry a single functional copy of the E. coli gpt gene. Fluorescence in situ hybridization (FISH) and digoxigenin-labeled probes, as smell as 673 bp, were used in an attempt to localize the 456 bp gpt gene to a specific chromosome. Chi-square analysis of 13 metaphases showed significant labeling on autosomal chromosomes 6 or 7, which are indistinguishable without further bonding analysis. Furthermore, a majority of the signals were on the q arm, proximal to the centromere. The data collected supports incorporation of the gpt gene into an acrocentric autosome of the AS52 cell line. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:176 / 180
页数:5
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