Multiple interactions between Scc1 and Scc2 activate cohesin's DNA dependent ATPase and replace Pds5 during loading

In addition to sharing with condensin an ability to organize DNA into chromatids, cohesin regulates enhancer-promoter interactions and confers sister chromatid cohesion. Association with chromosomes is regulated by hook-shaped HEAT repeat proteins that Associate With its Kleisin (Scc1) subunit (HAWK...

Full description

Saved in:
Bibliographic Details
Published inbioRxiv
Main Authors Petela, Naomi, Gligoris, Thomas G, Metson, Jean S, Byung-Gil, Lee, Voulgaris, Menelaos, Hu, Bin, Kikuchi, Sotaro, Chapard, Christophe, Chen, Wentao, Eeson Rajendra, Madhusudhan Srinivisan, Yu, Hongtao, Jan L we, Nasmyth, Kim
Format Paper
LanguageEnglish
Published Cold Spring Harbor Cold Spring Harbor Laboratory Press 19.10.2017
Subjects
Adenosine triphosphatase
Chromatids
Chromosomes
Cohesin
Condensin
Deoxyribonucleic acid
DNA
Mutation
Online AccessGet full text

Cover

More Information
Summary:In addition to sharing with condensin an ability to organize DNA into chromatids, cohesin regulates enhancer-promoter interactions and confers sister chromatid cohesion. Association with chromosomes is regulated by hook-shaped HEAT repeat proteins that Associate With its Kleisin (Scc1) subunit (HAWKs), namely Scc3, Pds5, and Scc2. Unlike Pds5, Scc2 is not a stable cohesin constituent but, as shown here, transiently displaces Pds5 during loading. Scc1 mutations that compromise its interaction with Scc2 adversely affect cohesin's ATPase activity, loading, and translocation while Scc2 mutations that alter how the ATPase responds to DNA abolish loading despite cohesin's initial association with loading sites. Lastly, Scc2 mutations that permit loading in the absence of Scc4 increase Scc2's association with chromosomal cohesin and reduce that of Pds5. We suggest that cohesin switches between two states, one with Pds5 bound to Scc1 that is not able to hydrolyse ATP efficiently but is capable of release from chromosomes and another in which Scc2, transiently replacing Pds5, stimulates the ATP hydrolysis necessary for loading and translocation away from loading sites.
DOI:10.1101/205914