Smc5/6 - microtubules binding shapes pericentromeric chromatin
Ànnia Carré SimoniD, Cecilia Martuzzi, Sarah IsleriD, Renaud BatriniD, Henrik Dahl PinholtiD, Timothy FöldesiD, Guillaume LaflammeiD, Juan RegueraiD, Maria Barbi, Leonid A. MirnyiD, Damien D’AmoursiD, Emmanuelle FabreiD
Abstract
Centromeres and pericentromeres are specialized chromatin regions essential for accurate chromosome segregation. Smc5/6, which localizes at pericentromeres, can bind microtubules, yet its role in chromatin folding is unclear. Here, we investigate the functional relevance of Smc5/6- microtubule binding in yeast, by targeting two lysines (K624, K631) within the Smc5 hinge domain known to mediate this binding. Using high-temporal-resolution imaging, polymer modelling, and in vitro approaches with a separation-of-function mutant smc5-2KE, we demonstrate that microtubules binding by Smc5/6 constrains chromatin dynamics and promotes pericentromeric folding. The smc5-2KE mutant, combined with a hypomorphic kinetochore mutant (Mtw1-3xGFP), leads to spindle and cytokinesis defects and triggers the spindle checkpoint. Furthermore, homologous recombination repair in pericentromeres is compromised. Overall, our findings indicate that Smc5/6 - microtubules association safeguard pericentromeric architecture and genome stability during mitosis.
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