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Abstract Studies on budding yeast have exposed the highly conserved mechanisms by which duplicated chromosomes are evenly distributed to daughter cells at the metaphase–anaphase transition. The establishment of proteinaceous bridges between sister chromatids, a function provided by a ring-shaped complex known as cohesin, is central to accurate segregation. It is the destruction of this cohesin that triggers the segregation of chromosomes following their proper attachment to microtubules. Since it is irreversible, this process must be tightly controlled and driven to completion. Furthermore, during meiosis, modifications must be put in place to allow the segregation of maternal and paternal chromosomes in the first division for gamete formation. Here, I review the pioneering work from budding yeast that has led to a molecular understanding of the establishment and destruction of cohesion.
Chromosomal Proteins, Non-Histone, YeastBook, Mitosis, Cell Cycle Proteins, Saccharomyces cerevisiae, Spindle Apparatus, Chromatids, Microtubules, Chromosomes, Meiosis, Chromosome Segregation, Kinetochores, Cohesins
Chromosomal Proteins, Non-Histone, YeastBook, Mitosis, Cell Cycle Proteins, Saccharomyces cerevisiae, Spindle Apparatus, Chromatids, Microtubules, Chromosomes, Meiosis, Chromosome Segregation, Kinetochores, Cohesins
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 88 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |