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Título
Structure of the cohesin loader Scc2.
Autor(es)
Palabras clave
Cell Cycle Proteins
Conserved Sequence
Models, Molecular
Protein Binding
Protein Subunits
Saccharomyces cerevisiae
accharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Clasificación UNESCO
24 Ciencias de la Vida
Fecha de publicación
2017-01-06
Citación
Chao, W. C., Murayama, Y., Muñoz, S., Jones, A. W., Wade, B. O., Purkiss, A. G., ... & Singleton, M. R. (2017). Structure of the cohesin loader Scc2. Nature communications, 8(1), 13952.
Resumen
[EN]The functions of cohesin are central to genome integrity, chromosome organization and transcription regulation through its prevention of premature sister-chromatid separation and the formation of DNA loops. The loading of cohesin onto chromatin depends on the Scc2-Scc4 complex; however, little is known about how it stimulates the cohesion-loading activity. Here we determine the large 'hook' structure of Scc2 responsible for catalysing cohesin loading. We identify key Scc2 surfaces that are crucial for cohesin loading in vivo. With the aid of previously determined structures and homology modelling, we derive a pseudo-atomic structure of the full-length Scc2-Scc4 complex. Finally, using recombinantly purified Scc2-Scc4 and cohesin, we performed crosslinking mass spectrometry and interaction assays that suggest Scc2-Scc4 uses its modular structure to make multiple contacts with cohesin.
URI
DOI
10.1038/ncomms13952
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