Related Experiment Video
Updated: Feb 20, 2026

High-throughput Screening for Protein-based Inheritance in S. cerevisiae
Published on: August 8, 2017
The yeast 2-μm plasmid Raf protein contributes to plasmid inheritance by stabilizing the Rep1 and Rep2 partitioning
Mary E McQuaid1, Jordan B Pinder1, Niroshaathevi Arumuggam1
1Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia B3H 4R2, Canada.
Abstract:
The yeast 2-μm 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 plasmid-encoded 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-μm plasmid.
Insights
The yeast 2-μm plasmid uses Rep proteins and Raf to ensure inheritance. Raf stabilizes Rep proteins, aiding plasmid partitioning and persistence, even when Rep interactions are impaired.
Area of Science:
- Molecular Biology
- Yeast Genetics
- Epigenetics
Background:
- The yeast 2-μm plasmid is a high-copy number genetic element crucial for host cell division.
- Efficient plasmid partitioning relies on Rep1, Rep2, and STB locus.
- Rep proteins and Raf regulate plasmid gene transcription.
Purpose of the Study:
- Identify domains and residues in Rep2 and Raf for protein association.
- Delineate the Rep2 DNA-binding domain.
- Understand the role of Raf in plasmid maintenance.
Main Methods:
- Protein interaction assays
- Sequence analyses
- Mutational approaches
Main Results:
- Rep2 and Raf interactions with Rep1 and Rep2 were characterized.
- Rep1 promotes STB association and stabilizes Rep protein levels.
- Rep2 mutants impaired in self-association or Rep1 association maintained inheritance with functional Raf.
Conclusions:
- Rep protein complexes are essential for partitioning and transcriptional repression.
- Raf stabilizes Rep partitioning proteins, contributing to 2-μm plasmid persistence.
- Raf's role extends beyond transcriptional regulation to plasmid stability.
More Related Videos
10:39A Suppressor Screen for the Characterization of Genetic Links Regulating Chronological Lifespan in Saccharomyces cerevisiae
Published on: September 17, 2020
07:18Gene-targeted Random Mutagenesis to Select Heterochromatin-destabilizing Proteasome Mutants in Fission Yeast
Published on: May 15, 2018
Related Concept Videos
Restarting Stalled Replication Forks
Yeast Signaling
Plasmids
The Contractile Ring
A small GTPase, RhoA, controls the function and assembly of the contractile ring. RhoA belongs to the Ras superfamily of proteins. The activation of formins by RhoA promotes...
Conservative Site-specific Recombination and Phase Variation
The recognition sites for Cre recombinase called LoxP...
Rab Proteins
Rab proteins switch between a cytosolic, GDP-bound inactive state and a membrane-anchored, GTP-bound active state. By themselves, Rabs show slow rates of GDP/GTP exchange and GTP hydrolysis. Thus, Rab proteins are considered...