The yeast 2-μm plasmid Raf protein contributes to plasmid inheritance by stabilizing the Rep1 and Rep2 partitioning proteins

被引:10
|
作者
McQuaid, Mary E. [1 ]
Pinder, Jordan B. [1 ]
Arumuggam, Niroshaathevi [1 ]
Lacoste, Jessica S. C. [1 ]
Chew, Joyce S. K. [1 ]
Dobson, Melanie J. [1 ]
机构
[1] Dalhousie Univ, Dept Biochem & Mol Biol, Halifax, NS B3H 4R2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
2 MICRON PLASMID; SACCHAROMYCES-CEREVISIAE; CIRCLE PLASMID; CIRCULAR PLASMID; CHROMOSOME SEGREGATION; STABLE MAINTENANCE; COPY NUMBER; DNA; LOCUS; KLUYVEROMYCES;
D O I
10.1093/nar/gkx703
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The yeast 2-mu m plasmid is a remarkable genetic parasite, managing efficient maintenance at high-copy number with minimal impact on the host. Equal partitioning of the plasmid upon host cell division requires plasmid proteins Rep1 and Rep2 and the plasmid STB locus. The Rep proteins and the plasmidencoded Raf protein also regulate plasmid gene transcription. In this study, protein interaction assays, sequence analyses and mutational approaches were used to identify domains and residues in Rep2 and Raf required for association with Rep1 and Rep2 and to delineate the Rep2 DNA-binding domain. Rep2 and Raf displayed similarities in interactions with Rep1 and Rep2, in having Rep1 promote their STB association in vivo, and in stabilizing Rep protein levels. Rep2 mutants impaired for self-association were competent for transcriptional repression while those deficient for Rep1 association were not. Surprisingly, Rep2 mutants impaired for either Rep1 interaction or self-association were able to maintain efficient plasmid inheritance provided Raf was present and competent for Rep protein interaction. Our findings provide insight into the Rep protein complexes required for partitioning and transcriptional repression, and suggest that in addition to its transcriptional function, Raf stabilization of Rep partitioning proteins contributes to the remarkable persistence of the 2 mu m plasmid.
引用
收藏
页码:10518 / 10533
页数:16
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