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RAD5a and REV3 function in two alternative pathways of DNA-damage tolerance in Arabidopsis
- Source :
- DNA Repair. 10:620-628
- Publication Year :
- 2011
- Publisher :
- Elsevier BV, 2011.
-
Abstract
- DNA-damage tolerance (DDT) in yeast is composed of two parallel pathways and mediated by sequential ubiquitinations of PCNA. While monoubiquitination of PCNA promotes translesion synthesis (TLS) that is dependent on polymerase ΞΆ consisted of a catalytic subunit Rev3 and a regulatory subunit Rev7, polyubiquitination of PCNA by Mms2-Ubc13-Rad5 promotes error-free lesion bypass. Inactivation of these two pathways results in a synergistic effect on DNA-damage responses; however, this two-branch DDT model has not been reported in any multicellular organisms. In order to examine whether Arabidopsis thaliana possesses a two-branch DDT system, we created rad5a rev3 double mutant plant lines and compared them with the corresponding single mutants. Arabidopsis rad5a and rev3 mutations are indeed synergistic with respect to root growth inhibition induced by replication-blocking lesions, suggesting that AtRAD5a and AtREV3 are required for error-free and TLS branches of DDT, respectively. Unexpectedly this study reveals three modes of genetic interactions in response to different types of DNA damage, implying that plant RAD5 and REV3 are also involved in DNA damage responses independent of DDT. By comparing with yeast cells, it is apparent that plant TLS is a more frequently utilized means of lesion bypass than error-free DDT in plants.
- Subjects :
- DNA damage
Mutant
Arabidopsis
DNA-Directed DNA Polymerase
medicine.disease_cause
Biochemistry
chemistry.chemical_compound
Gene Expression Regulation, Plant
medicine
Arabidopsis thaliana
Molecular Biology
Polymerase
Genetics
Mutation
biology
Arabidopsis Proteins
Cell Biology
biology.organism_classification
Cell biology
Proliferating cell nuclear antigen
chemistry
biology.protein
DNA
DNA Damage
Subjects
Details
- ISSN :
- 15687864
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- DNA Repair
- Accession number :
- edsair.doi.dedup.....115f8ec68777c25f81f7959b6d88a7ba
- Full Text :
- https://doi.org/10.1016/j.dnarep.2011.04.009