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Heat shock transcription factors demonstrate a distinct mode of interaction with mitotic chromosomes

A large number of transcription factors have been shown to bind and interact with mitotic chromosomes, which may promote the efficient reactivation of transcriptional programs following cell division. Although the DNA-binding domain (DBD) contributes strongly to TF behavior, the mitotic behaviors of...

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Autores principales: Price, Rachel M, Budzyński, Marek A, Shen, Junzhou, Mitchell, Jennifer E, Kwan, James Z J, Teves, Sheila S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250243/
https://www.ncbi.nlm.nih.gov/pubmed/37114996
http://dx.doi.org/10.1093/nar/gkad304
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author Price, Rachel M
Budzyński, Marek A
Shen, Junzhou
Mitchell, Jennifer E
Kwan, James Z J
Teves, Sheila S
author_facet Price, Rachel M
Budzyński, Marek A
Shen, Junzhou
Mitchell, Jennifer E
Kwan, James Z J
Teves, Sheila S
author_sort Price, Rachel M
collection PubMed
description A large number of transcription factors have been shown to bind and interact with mitotic chromosomes, which may promote the efficient reactivation of transcriptional programs following cell division. Although the DNA-binding domain (DBD) contributes strongly to TF behavior, the mitotic behaviors of TFs from the same DBD family may vary. To define the mechanisms governing TF behavior during mitosis in mouse embryonic stem cells, we examined two related TFs: Heat Shock Factor 1 and 2 (HSF1 and HSF2). We found that HSF2 maintains site-specific binding genome-wide during mitosis, whereas HSF1 binding is somewhat decreased. Surprisingly, live-cell imaging shows that both factors appear excluded from mitotic chromosomes to the same degree, and are similarly more dynamic in mitosis than in interphase. Exclusion from mitotic DNA is not due to extrinsic factors like nuclear import and export mechanisms. Rather, we found that the HSF DBDs can coat mitotic chromosomes, and that HSF2 DBD is able to establish site-specific binding. These data further confirm that site-specific binding and chromosome coating are independent properties, and that for some TFs, mitotic behavior is largely determined by the non-DBD regions.
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spelling pubmed-102502432023-06-10 Heat shock transcription factors demonstrate a distinct mode of interaction with mitotic chromosomes Price, Rachel M Budzyński, Marek A Shen, Junzhou Mitchell, Jennifer E Kwan, James Z J Teves, Sheila S Nucleic Acids Res Molecular Biology A large number of transcription factors have been shown to bind and interact with mitotic chromosomes, which may promote the efficient reactivation of transcriptional programs following cell division. Although the DNA-binding domain (DBD) contributes strongly to TF behavior, the mitotic behaviors of TFs from the same DBD family may vary. To define the mechanisms governing TF behavior during mitosis in mouse embryonic stem cells, we examined two related TFs: Heat Shock Factor 1 and 2 (HSF1 and HSF2). We found that HSF2 maintains site-specific binding genome-wide during mitosis, whereas HSF1 binding is somewhat decreased. Surprisingly, live-cell imaging shows that both factors appear excluded from mitotic chromosomes to the same degree, and are similarly more dynamic in mitosis than in interphase. Exclusion from mitotic DNA is not due to extrinsic factors like nuclear import and export mechanisms. Rather, we found that the HSF DBDs can coat mitotic chromosomes, and that HSF2 DBD is able to establish site-specific binding. These data further confirm that site-specific binding and chromosome coating are independent properties, and that for some TFs, mitotic behavior is largely determined by the non-DBD regions. Oxford University Press 2023-04-28 /pmc/articles/PMC10250243/ /pubmed/37114996 http://dx.doi.org/10.1093/nar/gkad304 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Price, Rachel M
Budzyński, Marek A
Shen, Junzhou
Mitchell, Jennifer E
Kwan, James Z J
Teves, Sheila S
Heat shock transcription factors demonstrate a distinct mode of interaction with mitotic chromosomes
title Heat shock transcription factors demonstrate a distinct mode of interaction with mitotic chromosomes
title_full Heat shock transcription factors demonstrate a distinct mode of interaction with mitotic chromosomes
title_fullStr Heat shock transcription factors demonstrate a distinct mode of interaction with mitotic chromosomes
title_full_unstemmed Heat shock transcription factors demonstrate a distinct mode of interaction with mitotic chromosomes
title_short Heat shock transcription factors demonstrate a distinct mode of interaction with mitotic chromosomes
title_sort heat shock transcription factors demonstrate a distinct mode of interaction with mitotic chromosomes
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250243/
https://www.ncbi.nlm.nih.gov/pubmed/37114996
http://dx.doi.org/10.1093/nar/gkad304
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