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Human p53 cellular tumor antigen: cDNA sequence and expression in COS cells
The EMBO Journal
|May 1, 1985
Summary
Researchers isolated a human p53 tumor antigen cDNA clone. This clone directs the production of a 55 kd polypeptide recognized by p53 antibodies, advancing cancer antigen research.
Area of Science:
- Molecular Biology
- Oncology
- Immunology
Background:
- The p53 tumor antigen is a critical factor in cellular regulation and cancer development.
- Understanding the molecular characteristics of human p53 is essential for cancer research and therapeutic development.
Purpose of the Study:
- To isolate and characterize the complementary DNA (cDNA) clone for human p53 tumor antigen.
- To compare the human p53 sequence with its mouse counterpart and assess its functional expression.
Main Methods:
- Isolation of a 2.5-kb cDNA clone encoding the full coding region of human p53.
- Nucleotide sequence comparison between human and mouse p53.
- Expression of the human p53 cDNA in SV40-based vectors.
- Analysis of the produced polypeptide using monoclonal antibodies against p53.
Main Results:
- A 2.5-kb cDNA clone for human p53 was successfully isolated, containing the complete coding sequence.
- Human p53 comprises 393 residues, differing from mouse p53 by six additional codons in exon 4.
- DNA sequence homology between human and mouse p53 coding regions is 81%, with uneven conservation.
- Expressed human p53 cDNA produced a 55 kd polypeptide, precipitable by anti-p53 monoclonal antibodies.
Conclusions:
- The isolated human p53 cDNA clone is functional and directs the synthesis of a recognizable p53 polypeptide.
- Sequence comparison reveals significant homology but also species-specific differences in p53 structure.
- This research provides a valuable tool for further investigation into p53's role in tumorigenesis and potential therapeutic strategies.