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A mechanism of gene amplification driven by small DNA fragments
Kuntal Mukherjee1, Francesca Storici
1School of Biology, Georgia Institute of Technology, Atlanta, Georgia, United States of America.
Abstract:
DNA amplification is a molecular process that increases the copy number of a chromosomal tract and often causes elevated expression of the amplified gene(s). Although gene amplification is frequently observed in cancer and other degenerative disorders, the molecular mechanisms involved in the process of DNA copy number increase remain largely unknown. We hypothesized that small DNA fragments could be the trigger of DNA amplification events. Following our findings that small fragments of DNA in the form of DNA oligonucleotides can be highly recombinogenic, we have developed a system in the yeast Saccharomyces cerevisiae to capture events of chromosomal DNA amplification initiated by small DNA fragments. Here we demonstrate that small DNAs can amplify a chromosomal region, generating either tandem duplications or acentric extrachromosomal DNA circles. Small fragment-driven DNA amplification (SFDA) occurs with a frequency that increases with the length of homology between the small DNAs and the target chromosomal regions. SFDA events are triggered even by small single-stranded molecules with as little as 20-nt homology with the genomic target. A double-strand break (DSB) external to the chromosomal amplicon region stimulates the amplification event up to a factor of 20 and favors formation of extrachromosomal circles. SFDA is dependent on Rad52 and Rad59, partially dependent on Rad1, Rad10, and Pol32, and independent of Rad51, suggesting a single-strand annealing mechanism. Our results reveal a novel molecular model for gene amplification, in which small DNA fragments drive DNA amplification and define the boundaries of the amplicon region. As DNA fragments are frequently found both inside cells and in the extracellular environment, such as the serum of patients with cancer or other degenerative disorders, we propose that SFDA may be a common mechanism for DNA amplification in cancer cells, as well as a more general cause of DNA copy number variation in nature.
Insights
Small DNA fragments can trigger DNA amplification, forming tandem duplications or extrachromosomal circles. This process, called small fragment-driven DNA amplification (SFDA), offers a new model for gene amplification in cancer and other disorders.
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- DNA amplification increases gene copy number, often linked to cancer, but mechanisms are unclear.
- Small DNA fragments, particularly oligonucleotides, are recombinogenic.
- Existing models do not fully explain DNA copy number increase.
Purpose of the Study:
- To investigate if small DNA fragments can initiate chromosomal DNA amplification.
- To develop a system in yeast to study small fragment-driven DNA amplification (SFDA).
- To elucidate the molecular mechanisms underlying SFDA.
Main Methods:
- Developed a yeast (Saccharomyces cerevisiae) system to capture DNA amplification events.
- Assessed amplification frequency based on homology length and DNA fragment characteristics (single-stranded vs. double-stranded).
- Investigated the role of DNA repair proteins (Rad52, Rad59, Rad1, Rad10, Pol32, Rad51) in SFDA.
Main Results:
- Demonstrated that small DNA fragments can induce chromosomal DNA amplification, forming tandem duplications or extrachromosomal circles.
- SFDA frequency correlates with homology length and is triggered by short single-stranded DNA.
- A double-strand break (DSB) significantly enhances SFDA and favors circle formation.
- SFDA relies on Rad52 and Rad59, suggesting a single-strand annealing mechanism.
Conclusions:
- Small DNA fragments are novel triggers for DNA amplification, defining amplicon boundaries.
- SFDA provides a new molecular model for gene amplification.
- This mechanism may contribute to DNA copy number variation in cancer and other conditions.
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