𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Expression of a methotrexate resistant dihydrofolate reductase gene in transgenic mice

✍ Scribed by Isola, Luis M. ;Gordon, Jon W.


Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
750 KB
Volume
10
Category
Article
ISSN
0192-253X

No coin nor oath required. For personal study only.

✦ Synopsis


We have previously demonstrated systemic resistance to methotrexate (MTX) in transgenic mice carrying a foreign, mutant dihydrofolate reductase (DHFR, E.C. 1 S.1.3) gene. The new gene was introduced as a cDNA cloned into an expression vector driven by the simian virus 40 (SV40) early promoter. Previous physiologic studies suggested that transgenic mice tolerated drug doses invariably lethal to controls on the basis of gastrointestinal (GI) resistance to MTX. In the present study we evaluated foreign gene expression at the RNA level in the three major sites o f MTX toxicity: intestine, liver, and bone marrow.

The transgene was transcriptionally active in small bowel, and levels of expression were high in animals tolerating the largest doses of MTX. The gene was also expressed in the liver in some pedigrees, but was not detected in hemopoietic tissues of any of the pedigrees tested. Our studies correlate the site of expression of a drug resistant dhfr gene with an altered physiologic response to MTX, and demonstrate that transgenic mice can be used as a test system for expression of genes considered for use in somatic gene therapy.


πŸ“œ SIMILAR VOLUMES


Regulation of dihydrofolate reductase ge
✍ Jin-Shyun Ruth Wu; Lee F. Johnson πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 English βš– 756 KB

## Abstract We have used a methotrexate‐resistant mouse 3T6 cell line (M50L3) that overproduces dihydrofolate reductase (DHFR) and its mRNA by a factor of about 300 to study the regulation of DHFR hnRNA synthesis. We have previously shown that when resting (G~0~) M50L3 cells are serum stimuled to r

Anemia in a line of transgenic mice carr
✍ Isola, Luis M. ;Gordon, Jon W. πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 694 KB

Several lines of transgenic mice were produced by pronuclear injection of a full-length cDNA encoding a mutant dihydrofolate reductase (DHFR, E.C. 1.5.1.3). The mutation causes altered enzyme kinetics for folate reduction as well as low affinity for methotrexate (MTX). One line of mice carrying the

Expression of human plasma protein genes
✍ Barbara H. Bowman; Funmei Yang; Gwendolyn S. Adrian πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 733 KB

Introduction of human plasma protein genes into the mouse genome to produce transgenic mice furnishes an in vivo model for correlating chromosomal DNA sequences with developmental and tissue-specific expression. The liver produces an array of plasma proteins that circulate throughout the body contri

Expression of the gene of interest fused
✍ Kubo, Jun ;Yamanouchi, Keitaro ;Naito, Kunihiko ;Tojo, Hideaki πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 137 KB

## Abstract The present paper describes the expression of a target fusion gene, WAP/hGH fused to the EGFP–expressing gene in transgenic mice derived from the transfer of transgenic embryos selected because of their expression of enhanced green fluorescent protein (EGFP). The 6.7–kb fusion gene was

Expression of a chimeric VIP gene is tar
✍ D. V. Agoston; D. T. Bravo; Dr. J. A. Waschek πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 720 KB

## Abstract We showed previously that a gene construction that consisted of 5.2 kb of 5' flanking sequence, the first exon, and part of the first intron of the human gene encoding vasoactive intestinal peptide (VIP) fused to the reporter gene chloramphenicol acetyltransferase (CAT) fully mimicked t