Related Experiment Video
Updated: Jul 28, 2026

Structure-function Studies in Mouse Embryonic Stem Cells Using Recombinase-mediated Cassette Exchange
Published on: April 27, 2017
Regulatory mutations in CHO cells induce expression of the mouse embryonic antigen SSEA-1
Abstract:
Two rare and dominant mutants of Chinese hamster ovary (CHO) cells, LEC11 and LEC12, express the mouse embryonic antigen SSEA-1. Parental CHO cells and the revertants, LEC11.R9 and LEC12.R10, do not express this antigen as detected by a sensitive radioimmunoassay with a monoclonal antibody to SSEA-1. The presence of the SSEA-1 determinant correlates with the apparent de novo expression of specific N-acetylglucosaminide alpha(1,3)fucosyltransferase activities not detected in parental or revertant cell extracts. Several differences in the enzymes substrate specificities and their products have been identified. The combined data suggest that LEC11 and LEC12 mutants result from regulatory mutations affecting different fucosyltransferase genes.
Insights
Two Chinese hamster ovary (CHO) cell mutants, LEC11 and LEC12, express the mouse embryonic antigen SSEA-1 due to regulatory mutations affecting fucosyltransferase genes. These mutants show distinct enzyme activities not present in parental cells or revertants.
Area of Science:
- Cell Biology
- Biochemistry
- Genetics
Background:
- Chinese hamster ovary (CHO) cells are a common model system in biological research.
- The mouse embryonic antigen SSEA-1 is a key developmental marker.
- Understanding mutations in cell lines aids in deciphering gene regulation.
Purpose of the Study:
- To investigate the molecular basis of SSEA-1 expression in CHO cell mutants.
- To identify the specific enzymatic activities associated with SSEA-1 expression.
- To explore the genetic regulation of fucosyltransferase genes.
Main Methods:
- Utilized radioimmunoassay with monoclonal antibodies to detect SSEA-1.
- Analyzed N-acetylglucosaminide alpha(1,3)fucosyltransferase activities in cell extracts.
- Compared enzyme substrate specificities and products between mutants and parental cells.
Main Results:
- LEC11 and LEC12 CHO cell mutants express the SSEA-1 antigen.
- Parental CHO cells and revertants (LEC11.R9, LEC12.R10) do not express SSEA-1.
- SSEA-1 expression correlates with the de novo activity of specific N-acetylglucosaminide alpha(1,3)fucosyltransferases.
- Differences in enzyme substrate specificities and products were observed.
Conclusions:
- LEC11 and LEC12 mutants likely arise from regulatory mutations.
- These mutations affect distinct fucosyltransferase genes.
- The study provides insights into the genetic control of SSEA-1 expression and fucosylation in CHO cells.
More Related Videos
09:32Light-mediated Reversible Modulation of the Mitogen-activated Protein Kinase Pathway during Cell Differentiation and Xenopus Embryonic Development
Published on: June 15, 2017
09:14Single-Cell RNA Sequencing of Mutant Whole Mouse Embryos: From the Epiblast to the End of Gastrulation
Published on: June 14, 2024
Related Concept Videos
In-vitro Mutagenesis
Determination
Cis-regulatory Sequences
Master Transcription Regulators