A selfish DNA element engages a meiosis-specific motor and telomeres for germ-line propagation
Soumitra Sau1, Michael N Conrad2, Chih-Ying Lee2
1Department of Molecular Biosciences, University of Texas at Austin, Austin, TX 78712.
Abstract:
The chromosome-like mitotic stability of the yeast 2 micron plasmid is conferred by the plasmid proteins Rep1-Rep2 and the cis-acting locus STB, likely by promoting plasmid-chromosome association and segregation by hitchhiking. Our analysis reveals that stable plasmid segregation during meiosis requires the bouquet proteins Ndj1 and Csm4. Plasmid relocalization from the nuclear interior in mitotic cells to the periphery at or proximal to telomeres rises from early meiosis to pachytene. Analogous to chromosomes, the plasmid undergoes Csm4- and Ndj1-dependent rapid prophase movements with speeds comparable to those of telomeres. Lack of Ndj1 partially disrupts plasmid-telomere association without affecting plasmid colocalization with the telomere-binding protein Rap1. The plasmid appears to engage a meiosis-specific motor that orchestrates telomere-led chromosome movements for its telomere-associated segregation during meiosis I. This hitherto uncharacterized mode of germ-line transmission by a selfish genetic element signifies a mechanistic variation within the shared theme of chromosome-coupled plasmid segregation during mitosis and meiosis.
Insights
Yeast 2 micron plasmid segregation relies on bouquet proteins Ndj1 and Csm4 during meiosis. This selfish genetic element uses a meiosis-specific motor for telomere-associated germ-line transmission.
Area of Science:
- * Molecular Biology
- * Genetics
- * Cell Biology
Background:
- * The yeast 2 micron plasmid exhibits chromosome-like mitotic stability, mediated by Rep1-Rep2 proteins and the STB locus.
- * This stability is thought to involve plasmid-chromosome association and segregation via hitchhiking.
- * Stable segregation during meiosis, however, remained less understood.
Purpose of the Study:
- * To investigate the mechanisms governing the stable segregation of the yeast 2 micron plasmid during meiosis.
- * To identify key proteins and cellular processes involved in plasmid segregation in meiotic cells.
- * To elucidate how the plasmid achieves germ-line transmission.
Main Methods:
- * Analysis of plasmid segregation in yeast mutants lacking key meiotic proteins (Ndj1, Csm4).
- * Microscopy techniques to track plasmid and telomere localization and movement during meiosis.
- * Examination of plasmid association with telomere-binding proteins like Rap1.
Main Results:
- * Stable plasmid segregation during meiosis requires the bouquet proteins Ndj1 and Csm4.
- * The plasmid relocalizes to the nuclear periphery near telomeres during prophase.
- * Plasmid movement during prophase is dependent on Ndj1 and Csm4, mirroring telomere dynamics.
- * Ndj1 is crucial for plasmid-telomere association, while Rap1 colocalization is unaffected.
- * Evidence suggests the plasmid utilizes a meiosis-specific motor for telomere-led segregation.
Conclusions:
- * The yeast 2 micron plasmid employs a novel mechanism for germ-line transmission during meiosis.
- * This mechanism involves association with the meiotic chromosome segregation machinery via telomeres.
- * The plasmid leverages bouquet proteins Ndj1 and Csm4 for its segregation, similar to chromosomes.
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