Cargando…

Reorientation of INO80 on hexasomes reveals basis for mechanistic versatility

Unlike other chromatin remodelers, INO80 preferentially mobilizes hexasomes, which can form during transcription. Why INO80 prefers hexasomes over nucleosomes remains unclear. Here, we report structures of S. cerevisiae INO80 bound to a hexasome or a nucleosome. INO80 binds the two substrates in sub...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Hao, Muñoz, Elise N., Hsieh, Laura J., Chio, Un Seng, Gourdet, Muryam A., Narlikar, Geeta J., Cheng, Yifan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10480058/
https://www.ncbi.nlm.nih.gov/pubmed/37384669
http://dx.doi.org/10.1126/science.adf4197
_version_ 1785101717459697664
author Wu, Hao
Muñoz, Elise N.
Hsieh, Laura J.
Chio, Un Seng
Gourdet, Muryam A.
Narlikar, Geeta J.
Cheng, Yifan
author_facet Wu, Hao
Muñoz, Elise N.
Hsieh, Laura J.
Chio, Un Seng
Gourdet, Muryam A.
Narlikar, Geeta J.
Cheng, Yifan
author_sort Wu, Hao
collection PubMed
description Unlike other chromatin remodelers, INO80 preferentially mobilizes hexasomes, which can form during transcription. Why INO80 prefers hexasomes over nucleosomes remains unclear. Here, we report structures of S. cerevisiae INO80 bound to a hexasome or a nucleosome. INO80 binds the two substrates in substantially different orientations. On a hexasome, INO80 places its ATPase subunit, Ino80, at superhelical location (SHL)-2, across from SHL-6/−7 as previously seen on nucleosomes. Our results suggest that INO80 action on hexasomes resembles action by other remodelers on nucleosomes, such that Ino80 is maximally active near SHL-2. The SHL-2 position also plays a critical role for nucleosome remodeling by INO80. Overall, the mechanistic adaptations used by INO80 for preferential hexasome sliding imply that sub-nucleosomal particles play considerable regulatory roles.
format Online
Article
Text
id pubmed-10480058
institution National Center for Biotechnology Information
language English
publishDate 2023
record_format MEDLINE/PubMed
spelling pubmed-104800582023-09-05 Reorientation of INO80 on hexasomes reveals basis for mechanistic versatility Wu, Hao Muñoz, Elise N. Hsieh, Laura J. Chio, Un Seng Gourdet, Muryam A. Narlikar, Geeta J. Cheng, Yifan Science Article Unlike other chromatin remodelers, INO80 preferentially mobilizes hexasomes, which can form during transcription. Why INO80 prefers hexasomes over nucleosomes remains unclear. Here, we report structures of S. cerevisiae INO80 bound to a hexasome or a nucleosome. INO80 binds the two substrates in substantially different orientations. On a hexasome, INO80 places its ATPase subunit, Ino80, at superhelical location (SHL)-2, across from SHL-6/−7 as previously seen on nucleosomes. Our results suggest that INO80 action on hexasomes resembles action by other remodelers on nucleosomes, such that Ino80 is maximally active near SHL-2. The SHL-2 position also plays a critical role for nucleosome remodeling by INO80. Overall, the mechanistic adaptations used by INO80 for preferential hexasome sliding imply that sub-nucleosomal particles play considerable regulatory roles. 2023-07-21 2023-06-29 /pmc/articles/PMC10480058/ /pubmed/37384669 http://dx.doi.org/10.1126/science.adf4197 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License, which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Wu, Hao
Muñoz, Elise N.
Hsieh, Laura J.
Chio, Un Seng
Gourdet, Muryam A.
Narlikar, Geeta J.
Cheng, Yifan
Reorientation of INO80 on hexasomes reveals basis for mechanistic versatility
title Reorientation of INO80 on hexasomes reveals basis for mechanistic versatility
title_full Reorientation of INO80 on hexasomes reveals basis for mechanistic versatility
title_fullStr Reorientation of INO80 on hexasomes reveals basis for mechanistic versatility
title_full_unstemmed Reorientation of INO80 on hexasomes reveals basis for mechanistic versatility
title_short Reorientation of INO80 on hexasomes reveals basis for mechanistic versatility
title_sort reorientation of ino80 on hexasomes reveals basis for mechanistic versatility
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10480058/
https://www.ncbi.nlm.nih.gov/pubmed/37384669
http://dx.doi.org/10.1126/science.adf4197
work_keys_str_mv AT wuhao reorientationofino80onhexasomesrevealsbasisformechanisticversatility
AT munozelisen reorientationofino80onhexasomesrevealsbasisformechanisticversatility
AT hsiehlauraj reorientationofino80onhexasomesrevealsbasisformechanisticversatility
AT chiounseng reorientationofino80onhexasomesrevealsbasisformechanisticversatility
AT gourdetmuryama reorientationofino80onhexasomesrevealsbasisformechanisticversatility
AT narlikargeetaj reorientationofino80onhexasomesrevealsbasisformechanisticversatility
AT chengyifan reorientationofino80onhexasomesrevealsbasisformechanisticversatility