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Updated: Oct 3, 2026

Mouse Genome Engineering Using Designer Nucleases
Published on: April 2, 2014
[Expression in mouse L cells of mos-related ORAgp5 locus cloned from the human genome]
Abstract:
The recombinant locus ORAgp5 containing the regions homologous to protooncogene mos was previously cloned from the human genome. In order to monitor the expression of this human genome region, we have transfected the recombinant phage gp5 into mouse LMtk cells. One of these transfectants contained several copies of gp5. ORAgp5 sequences were found to be expressed in 1.5 kb RNA from this clone.
Insights
Researchers cloned the ORAgp5 locus from human DNA. Transfecting this into mouse cells revealed expression of ORAgp5 sequences as 1.5 kb RNA, aiding gene expression monitoring.
Area of Science:
- Molecular Biology
- Genomics
- Human Genetics
Background:
- The protooncogene mos is a key regulator of cell division.
- Understanding human genome regions homologous to mos is crucial for cancer research.
- The recombinant locus ORAgp5 was previously isolated from the human genome.
Purpose of the Study:
- To monitor the expression of the ORAgp5 human genome region.
- To establish a system for studying ORAgp5 gene regulation.
Main Methods:
- Cloning of the ORAgp5 locus from human DNA.
- Transfection of recombinant phage gp5 into mouse LMtk cells.
- Analysis of gene expression using RNA detection.
Main Results:
- Successful integration and amplification of multiple gp5 copies in mouse LMtk cells.
- Detection of ORAgp5 sequence expression.
- Identification of a 1.5 kb RNA transcript indicative of ORAgp5 expression.
Conclusions:
- The transfected mouse cell system effectively allows for monitoring of ORAgp5 expression.
- The 1.5 kb RNA represents a transcript from the ORAgp5 locus.
- This study provides a foundation for further investigation into the function and regulation of ORAgp5.

