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Structural convergence endows nuclear transport receptor Kap114p with a transcriptional repressor function toward TATA-binding protein

The transcription factor TATA-box binding protein (TBP) modulates gene expression in nuclei. This process requires the involvement of nuclear transport receptors, collectively termed karyopherin-β (Kap-β) in yeast, and various regulatory factors. In previous studies we showed that Kap114p, a Kap-β t...

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Autores principales: Liao, Chung-Chi, Wang, Yi-Sen, Pi, Wen-Chieh, Wang, Chun-Hsiung, Wu, Yi-Min, Chen, Wei-Yi, Hsia, Kuo-Chiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491584/
https://www.ncbi.nlm.nih.gov/pubmed/37684250
http://dx.doi.org/10.1038/s41467-023-41206-9
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author Liao, Chung-Chi
Wang, Yi-Sen
Pi, Wen-Chieh
Wang, Chun-Hsiung
Wu, Yi-Min
Chen, Wei-Yi
Hsia, Kuo-Chiang
author_facet Liao, Chung-Chi
Wang, Yi-Sen
Pi, Wen-Chieh
Wang, Chun-Hsiung
Wu, Yi-Min
Chen, Wei-Yi
Hsia, Kuo-Chiang
author_sort Liao, Chung-Chi
collection PubMed
description The transcription factor TATA-box binding protein (TBP) modulates gene expression in nuclei. This process requires the involvement of nuclear transport receptors, collectively termed karyopherin-β (Kap-β) in yeast, and various regulatory factors. In previous studies we showed that Kap114p, a Kap-β that mediates nuclear import of yeast TBP (yTBP), modulates yTBP-dependent transcription. However, how Kap114p associates with yTBP to exert its multifaceted functions has remained elusive. Here, we employ single-particle cryo-electron microscopy to determine the structure of Kap114p in complex with the core domain of yTBP (yTBP(C)). Remarkably, Kap114p wraps around the yTBP(C) N-terminal lobe, revealing a structure resembling transcriptional regulators in complex with TBP, suggesting convergent evolution of the two protein groups for a common function. We further demonstrate that Kap114p sequesters yTBP away from promoters, preventing a collapse of yTBP dynamics required for yeast responses to environmental stress. Hence, we demonstrate that nuclear transport receptors represent critical elements of the transcriptional regulatory network.
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spelling pubmed-104915842023-09-10 Structural convergence endows nuclear transport receptor Kap114p with a transcriptional repressor function toward TATA-binding protein Liao, Chung-Chi Wang, Yi-Sen Pi, Wen-Chieh Wang, Chun-Hsiung Wu, Yi-Min Chen, Wei-Yi Hsia, Kuo-Chiang Nat Commun Article The transcription factor TATA-box binding protein (TBP) modulates gene expression in nuclei. This process requires the involvement of nuclear transport receptors, collectively termed karyopherin-β (Kap-β) in yeast, and various regulatory factors. In previous studies we showed that Kap114p, a Kap-β that mediates nuclear import of yeast TBP (yTBP), modulates yTBP-dependent transcription. However, how Kap114p associates with yTBP to exert its multifaceted functions has remained elusive. Here, we employ single-particle cryo-electron microscopy to determine the structure of Kap114p in complex with the core domain of yTBP (yTBP(C)). Remarkably, Kap114p wraps around the yTBP(C) N-terminal lobe, revealing a structure resembling transcriptional regulators in complex with TBP, suggesting convergent evolution of the two protein groups for a common function. We further demonstrate that Kap114p sequesters yTBP away from promoters, preventing a collapse of yTBP dynamics required for yeast responses to environmental stress. Hence, we demonstrate that nuclear transport receptors represent critical elements of the transcriptional regulatory network. Nature Publishing Group UK 2023-09-08 /pmc/articles/PMC10491584/ /pubmed/37684250 http://dx.doi.org/10.1038/s41467-023-41206-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liao, Chung-Chi
Wang, Yi-Sen
Pi, Wen-Chieh
Wang, Chun-Hsiung
Wu, Yi-Min
Chen, Wei-Yi
Hsia, Kuo-Chiang
Structural convergence endows nuclear transport receptor Kap114p with a transcriptional repressor function toward TATA-binding protein
title Structural convergence endows nuclear transport receptor Kap114p with a transcriptional repressor function toward TATA-binding protein
title_full Structural convergence endows nuclear transport receptor Kap114p with a transcriptional repressor function toward TATA-binding protein
title_fullStr Structural convergence endows nuclear transport receptor Kap114p with a transcriptional repressor function toward TATA-binding protein
title_full_unstemmed Structural convergence endows nuclear transport receptor Kap114p with a transcriptional repressor function toward TATA-binding protein
title_short Structural convergence endows nuclear transport receptor Kap114p with a transcriptional repressor function toward TATA-binding protein
title_sort structural convergence endows nuclear transport receptor kap114p with a transcriptional repressor function toward tata-binding protein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491584/
https://www.ncbi.nlm.nih.gov/pubmed/37684250
http://dx.doi.org/10.1038/s41467-023-41206-9
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