Related Experiment Videos
Human elongation factor 1 alpha: a polymorphic and conserved multigene family with multiple chromosomal localizations
Human Genetics
|April 1, 1987
Summary
Human melanoma cells show increased elongation factor 1 alpha mRNA after phorbol ester treatment. This gene family is complex, with multiple copies and locations in the human genome.
Area of Science:
- Molecular Biology
- Cancer Research
- Genetics
Background:
- The tumor-promoting phorbol ester activates specific genes in human melanoma cells.
- Elongation factor 1 alpha (EF-1 alpha) is a key protein in protein synthesis.
Purpose of the Study:
- To investigate the role and characteristics of elongation factor 1 alpha in human melanoma.
- To analyze the gene structure, expression, and genomic organization of EF-1 alpha.
Main Methods:
- cDNA cloning and sequencing to analyze EF-1 alpha.
- Northern blot analysis to quantify mRNA levels.
- Southern blot analysis and in situ hybridization to study gene family and chromosomal localization.
Main Results:
- A cDNA clone for EF-1 alpha was isolated, showing homology with other species.
- Phorbol ester treatment induced a 3- to 5-fold increase in EF-1 alpha mRNA.
- Human genome contains a multi-gene family for EF-1 alpha with multiple chromosomal localizations and over ten copies per haploid genome.
Conclusions:
- Elongation factor 1 alpha is significantly upregulated in melanoma cells by phorbol ester.
- The human EF-1 alpha gene family is complex, indicating potential regulatory mechanisms.
- Understanding EF-1 alpha's genomic organization and expression is crucial for melanoma research.