Autonomous replication of foreign DNA in Histoplasma capsulatum: role of native telomeric sequences
1Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110.
Abstract:
Genetic transformation of the dimorphic pathogenic fungus Histoplasma capsulatum can result in chromosomal integration of the transforming DNA or the generation of multicopy linear plasmids carrying the transforming DNA. We showed previously that Escherichia coli plasmids do not replicate autonomously in H. capsulatum without significant modifications, one of which is the in vivo addition of Histoplasma telomeres at the termini of linear DNA. To address the requirements for autonomous replication in H. capsulatum, we constructed a circular E. coli plasmid containing adjacent inverted stretches of Histoplasma telomeric repeats separated by a unique restriction site. The linearized plasmid bearing telomeric termini was maintained in H. capsulatum without modification other than the addition of more telomeric sequence. We recovered the original plasmid in E. coli after removal of the telomeric termini by using engineered restriction sites. Thus, no special Histoplasma modification or sequence other than the telomeres was needed for autonomous replication in H. capsulatum. Additionally, this plasmid provides a shuttle vector that replicates autonomously in E. coli (as a circular plasmid) and in H. capsulatum (as a linear plasmid).
Insights
Histoplasma capsulatum genetic transformation can create plasmids. Researchers developed a shuttle vector, demonstrating that only Histoplasma telomeres are needed for autonomous replication in this fungus.
Area of Science:
- Mycology
- Molecular Biology
- Genetics
Background:
- Histoplasma capsulatum genetic transformation can lead to chromosomal integration or linear plasmid formation.
- Autonomous replication of Escherichia coli plasmids in H. capsulatum requires modifications, including adding Histoplasma telomeres.
Purpose of the Study:
- To investigate the requirements for autonomous DNA replication in Histoplasma capsulatum.
- To construct and validate a novel shuttle vector for H. capsulatum.
Main Methods:
- Engineered a circular E. coli plasmid with inverted Histoplasma telomeric repeats.
- Linearized the plasmid and introduced it into H. capsulatum.
- Recovered the plasmid from E. coli after telomere removal.
Main Results:
- The linearized plasmid with telomeric termini was maintained in H. capsulatum.
- No additional H. capsulatum-specific sequences were required for replication.
- The plasmid demonstrated autonomous replication in both E. coli and H. capsulatum.
Conclusions:
- Histoplasma telomeres are sufficient for autonomous replication of linear DNA in H. capsulatum.
- Developed a functional shuttle vector for genetic manipulation of H. capsulatum.
- Simplifies genetic transformation protocols for this pathogenic fungus.
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