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Published on: February 5, 2018
[cDNA cloning of a novel gene related to apoptosis by differential display RT-PCR]
1Burn Center, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
Objective:
To search for the novel gene related to apoptosis.
Methods:
The mRNA expression patterns of U937 cells treated with or without trichosanthin were compared with differential display RT-PCR. The cDNA, which was highly expressed in the apoptosis cells, was used as a probe to screen the human fetal liver cDNA library.
Results:
A 1.4 kb cDNA segment was the partial sequence of a novel gene related to apoptosis. The result of Northern blot showed three bands in the apoptosis cells. Some sequence of the 1.4 kb cDNA was homology to Bruton's tyrosine kinase.
Conclusion:
A partial cDNA of a new gene related to apoptosis was found.
Insights
Researchers identified a novel gene linked to apoptosis using differential display RT-PCR and cDNA library screening. This discovery advances understanding of programmed cell death mechanisms.
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Context:
- Apoptosis, or programmed cell death, is crucial for development and disease.
- Understanding the genes regulating apoptosis is key to therapeutic interventions.
Purpose:
- To identify novel genes involved in the process of apoptosis.
- To characterize the expression patterns of these genes in apoptotic cells.
Summary:
- Differential display RT-PCR was used to compare mRNA expression in U937 cells with and without trichosanthin treatment.
- A highly expressed cDNA fragment in apoptotic cells was identified and used to screen a human fetal liver cDNA library.
- A 1.4 kb partial cDNA sequence of a novel apoptosis-related gene was isolated, showing homology to Bruton's tyrosine kinase.
Impact:
- This finding contributes to the identification of new molecular players in apoptosis.
- The discovered gene may serve as a potential target for future research in cancer and other diseases involving apoptosis dysregulation.

