Back to Search
Start Over
Natural variation in a single amino acid underlies cellular responses to topoisomerase II poisons
- Publication Year :
- 2017
- Publisher :
- Cold Spring Harbor Laboratory, 2017.
-
Abstract
- Many medications, including chemotherapeutics, are differentially effective from one patient to the next. Understanding the causes of these population-wide differences is a critical step towards the development of personalized treatments and improvements to existing medications. Here, we investigate natural differences in sensitivity to anti-neoplastic drugs that target topoisomerase II, using the model organismCaenorhabditis elegans. We show that wild isolates ofC. elegansvary in their sensitivity to these drugs, and we use an unbiased statistical and molecular genetics approach to demonstrate that this variation is explained by a methionine-to-glutamine substitution in topoisomerase II (TOP-2). The presence of a non-polar methionine at this residue increases hydrophobic interactions between TOP-2 and the poison etoposide, as compared to a polar glutamine. We hypothesize that this stabilizing interaction results in increased genomic instability in strains that contain a methionine residue. The residue affected by this substitution is conserved from yeast to humans and is one of the few differences between the two human topoisomerase II isoforms (methionine in hTOPIIα and glutamine in hTOPIIβ). We go on to show that this substitution influences binding and cytotoxicity of etoposide and two additional topoisomerase II poisons in human cell lines. These results explain why hTOPIIα and hTOPIIβ are differentially affected by various poisons and demonstrate the utility ofC. elegansin understanding the genetics of drug responses.
- Subjects :
- Genetics
Genome instability
medicine.medical_specialty
Methionine
biology
ved/biology
Topoisomerase
ved/biology.organism_classification_rank.species
biology.organism_classification
Glutamine
chemistry.chemical_compound
Biochemistry
chemistry
Molecular genetics
biology.protein
medicine
Model organism
Etoposide
Caenorhabditis elegans
medicine.drug
Subjects
Details
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....09f281fc1fae2a16dbe95af65dbec1cb