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Chromosome segregation in Archaea: SegA– and SegB–DNA complex structures provide insights into segrosome assembly

Genome segregation is a vital process in all organisms. Chromosome partitioning remains obscure in Archaea, the third domain of life. Here, we investigated the SegAB system from Sulfolobus solfataricus. SegA is a ParA Walker-type ATPase and SegB is a site-specific DNA-binding protein. We determined...

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Autores principales: Yen, Cheng-Yi, Lin, Min-Guan, Chen, Bo-Wei, Ng, Irene W, Read, Nicholas, Kabli, Azhar F, Wu, Che-Ting, Shen, Yo-You, Chen, Chen-Hao, Barillà, Daniela, Sun, Yuh-Ju, Hsiao, Chwan-Deng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8682754/
https://www.ncbi.nlm.nih.gov/pubmed/34850144
http://dx.doi.org/10.1093/nar/gkab1155
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author Yen, Cheng-Yi
Lin, Min-Guan
Chen, Bo-Wei
Ng, Irene W
Read, Nicholas
Kabli, Azhar F
Wu, Che-Ting
Shen, Yo-You
Chen, Chen-Hao
Barillà, Daniela
Sun, Yuh-Ju
Hsiao, Chwan-Deng
author_facet Yen, Cheng-Yi
Lin, Min-Guan
Chen, Bo-Wei
Ng, Irene W
Read, Nicholas
Kabli, Azhar F
Wu, Che-Ting
Shen, Yo-You
Chen, Chen-Hao
Barillà, Daniela
Sun, Yuh-Ju
Hsiao, Chwan-Deng
author_sort Yen, Cheng-Yi
collection PubMed
description Genome segregation is a vital process in all organisms. Chromosome partitioning remains obscure in Archaea, the third domain of life. Here, we investigated the SegAB system from Sulfolobus solfataricus. SegA is a ParA Walker-type ATPase and SegB is a site-specific DNA-binding protein. We determined the structures of both proteins and those of SegA–DNA and SegB–DNA complexes. The SegA structure revealed an atypical, novel non-sandwich dimer that binds DNA either in the presence or in the absence of ATP. The SegB structure disclosed a ribbon–helix–helix motif through which the protein binds DNA site specifically. The association of multiple interacting SegB dimers with the DNA results in a higher order chromatin-like structure. The unstructured SegB N-terminus plays an essential catalytic role in stimulating SegA ATPase activity and an architectural regulatory role in segrosome (SegA–SegB–DNA) formation. Electron microscopy results also provide a compact ring-like segrosome structure related to chromosome organization. These findings contribute a novel mechanistic perspective on archaeal chromosome segregation.
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spelling pubmed-86827542021-12-20 Chromosome segregation in Archaea: SegA– and SegB–DNA complex structures provide insights into segrosome assembly Yen, Cheng-Yi Lin, Min-Guan Chen, Bo-Wei Ng, Irene W Read, Nicholas Kabli, Azhar F Wu, Che-Ting Shen, Yo-You Chen, Chen-Hao Barillà, Daniela Sun, Yuh-Ju Hsiao, Chwan-Deng Nucleic Acids Res Structural Biology Genome segregation is a vital process in all organisms. Chromosome partitioning remains obscure in Archaea, the third domain of life. Here, we investigated the SegAB system from Sulfolobus solfataricus. SegA is a ParA Walker-type ATPase and SegB is a site-specific DNA-binding protein. We determined the structures of both proteins and those of SegA–DNA and SegB–DNA complexes. The SegA structure revealed an atypical, novel non-sandwich dimer that binds DNA either in the presence or in the absence of ATP. The SegB structure disclosed a ribbon–helix–helix motif through which the protein binds DNA site specifically. The association of multiple interacting SegB dimers with the DNA results in a higher order chromatin-like structure. The unstructured SegB N-terminus plays an essential catalytic role in stimulating SegA ATPase activity and an architectural regulatory role in segrosome (SegA–SegB–DNA) formation. Electron microscopy results also provide a compact ring-like segrosome structure related to chromosome organization. These findings contribute a novel mechanistic perspective on archaeal chromosome segregation. Oxford University Press 2021-11-29 /pmc/articles/PMC8682754/ /pubmed/34850144 http://dx.doi.org/10.1093/nar/gkab1155 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Structural Biology
Yen, Cheng-Yi
Lin, Min-Guan
Chen, Bo-Wei
Ng, Irene W
Read, Nicholas
Kabli, Azhar F
Wu, Che-Ting
Shen, Yo-You
Chen, Chen-Hao
Barillà, Daniela
Sun, Yuh-Ju
Hsiao, Chwan-Deng
Chromosome segregation in Archaea: SegA– and SegB–DNA complex structures provide insights into segrosome assembly
title Chromosome segregation in Archaea: SegA– and SegB–DNA complex structures provide insights into segrosome assembly
title_full Chromosome segregation in Archaea: SegA– and SegB–DNA complex structures provide insights into segrosome assembly
title_fullStr Chromosome segregation in Archaea: SegA– and SegB–DNA complex structures provide insights into segrosome assembly
title_full_unstemmed Chromosome segregation in Archaea: SegA– and SegB–DNA complex structures provide insights into segrosome assembly
title_short Chromosome segregation in Archaea: SegA– and SegB–DNA complex structures provide insights into segrosome assembly
title_sort chromosome segregation in archaea: sega– and segb–dna complex structures provide insights into segrosome assembly
topic Structural Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8682754/
https://www.ncbi.nlm.nih.gov/pubmed/34850144
http://dx.doi.org/10.1093/nar/gkab1155
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