Evidence for cohesin sliding along budding yeast chromosomes.

[EN]The ring-shaped cohesin complex is thought to topologically hold sister chromatids together from their synthesis in S phase until chromosome segregation in mitosis. How cohesin stably binds to chromosomes for extended periods, without impeding other chromosomal processes that also require access...

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Detalles Bibliográficos
Autores: Ocampo Hafalla, María, Muñoz Félix, Sofía, Samora, Catarina P, Uhlmann, Frank
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2016
País:España
Institución:Universidad de Salamanca (USAL)
Repositorio:GREDOS. Repositorio Institucional de la Universidad de Salamanca
OAI Identifier:oai:gredos.usal.es:10366/154883
Acceso en línea:http://hdl.handle.net/10366/154883
Access Level:acceso abierto
Palabra clave:Cohesina
Estabilidad del genoma
Cohesión de cromáticas hermanas
Saccharomyces cerevisiae Proteins
DNA Replication
Monosaccharide Transport Proteins
Saccharomycetales
Chromosomes
Cysteine Synthase
Chromosome Segregation
HSP70 Heat-Shock Proteins
Mitochondrial Proteins
Transcriptional Activation
Cell Cycle Proteins
24 Ciencias de la Vida
proteínas mitocondriales
proteínas de Saccharomyces cerevisiae
cisteína sintasa
proteínas de transporte de monosacáridos
proteínas del ciclo celular
activación transcripcional
cromosomas
replicación del ADN
proteínas de choque térmico HSP70
segregación cromosómica
Descripción
Sumario:[EN]The ring-shaped cohesin complex is thought to topologically hold sister chromatids together from their synthesis in S phase until chromosome segregation in mitosis. How cohesin stably binds to chromosomes for extended periods, without impeding other chromosomal processes that also require access to the DNA, is poorly understood. Budding yeast cohesin is loaded onto DNA by the Scc2-Scc4 cohesin loader at centromeres and promoters of active genes, from where cohesin translocates to more permanent places of residence at transcription termination sites. Here we show that, at the GAL2 and MET17 loci, pre-existing cohesin is pushed downstream along the DNA in response to transcriptional gene activation, apparently without need for intermittent dissociation or reloading. We observe translocation intermediates and find that the distribution of most chromosomal cohesin is shaped by transcription. Our observations support a model in which cohesin is able to slide laterally along chromosomes while maintaining topological contact with DNA. In this way, stable cohesin binding to DNA and enduring sister chromatid cohesion become compatible with simultaneous underlying chromosomal activities, including but maybe not limited to transcription.