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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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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 |
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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 |
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