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Homeodomain-Interacting Protein Kinase (HPK-1) regulates stress responses and ageing in C. elegans
Proteins of the Homeodomain-Interacting Protein Kinase (HIPK) family regulate an array of processes in mammalian systems, such as the DNA damage response, cellular proliferation and apoptosis. The nematode Caenorhabditis elegans has a single HIPK homologue called HPK-1. Previous studies have implica...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726358/ https://www.ncbi.nlm.nih.gov/pubmed/26791749 http://dx.doi.org/10.1038/srep19582 |
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author | Berber, Slavica Wood, Mallory Llamosas, Estelle Thaivalappil, Priya Lee, Karen Liao, Bing Mana Chew, Yee Lian Rhodes, Aaron Yucel, Duygu Crossley, Merlin Nicholas, Hannah R |
author_facet | Berber, Slavica Wood, Mallory Llamosas, Estelle Thaivalappil, Priya Lee, Karen Liao, Bing Mana Chew, Yee Lian Rhodes, Aaron Yucel, Duygu Crossley, Merlin Nicholas, Hannah R |
author_sort | Berber, Slavica |
collection | PubMed |
description | Proteins of the Homeodomain-Interacting Protein Kinase (HIPK) family regulate an array of processes in mammalian systems, such as the DNA damage response, cellular proliferation and apoptosis. The nematode Caenorhabditis elegans has a single HIPK homologue called HPK-1. Previous studies have implicated HPK-1 in longevity control and suggested that this protein may be regulated in a stress-dependent manner. Here we set out to expand these observations by investigating the role of HPK-1 in longevity and in the response to heat and oxidative stress. We find that levels of HPK-1 are regulated by heat stress, and that HPK-1 contributes to survival following heat or oxidative stress. Additionally, we show that HPK-1 is required for normal longevity, with loss of HPK-1 function leading to a faster decline of physiological processes that reflect premature ageing. Through microarray analysis, we have found that HPK-1-regulated genes include those encoding proteins that serve important functions in stress responses such as Phase I and Phase II detoxification enzymes. Consistent with a role in longevity assurance, HPK-1 also regulates the expression of age-regulated genes. Lastly, we show that HPK-1 functions in the same pathway as DAF-16 to regulate longevity and reveal a new role for HPK-1 in development. |
format | Online Article Text |
id | pubmed-4726358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47263582016-01-27 Homeodomain-Interacting Protein Kinase (HPK-1) regulates stress responses and ageing in C. elegans Berber, Slavica Wood, Mallory Llamosas, Estelle Thaivalappil, Priya Lee, Karen Liao, Bing Mana Chew, Yee Lian Rhodes, Aaron Yucel, Duygu Crossley, Merlin Nicholas, Hannah R Sci Rep Article Proteins of the Homeodomain-Interacting Protein Kinase (HIPK) family regulate an array of processes in mammalian systems, such as the DNA damage response, cellular proliferation and apoptosis. The nematode Caenorhabditis elegans has a single HIPK homologue called HPK-1. Previous studies have implicated HPK-1 in longevity control and suggested that this protein may be regulated in a stress-dependent manner. Here we set out to expand these observations by investigating the role of HPK-1 in longevity and in the response to heat and oxidative stress. We find that levels of HPK-1 are regulated by heat stress, and that HPK-1 contributes to survival following heat or oxidative stress. Additionally, we show that HPK-1 is required for normal longevity, with loss of HPK-1 function leading to a faster decline of physiological processes that reflect premature ageing. Through microarray analysis, we have found that HPK-1-regulated genes include those encoding proteins that serve important functions in stress responses such as Phase I and Phase II detoxification enzymes. Consistent with a role in longevity assurance, HPK-1 also regulates the expression of age-regulated genes. Lastly, we show that HPK-1 functions in the same pathway as DAF-16 to regulate longevity and reveal a new role for HPK-1 in development. Nature Publishing Group 2016-01-21 /pmc/articles/PMC4726358/ /pubmed/26791749 http://dx.doi.org/10.1038/srep19582 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Berber, Slavica Wood, Mallory Llamosas, Estelle Thaivalappil, Priya Lee, Karen Liao, Bing Mana Chew, Yee Lian Rhodes, Aaron Yucel, Duygu Crossley, Merlin Nicholas, Hannah R Homeodomain-Interacting Protein Kinase (HPK-1) regulates stress responses and ageing in C. elegans |
title | Homeodomain-Interacting Protein Kinase (HPK-1) regulates stress responses and ageing in C. elegans |
title_full | Homeodomain-Interacting Protein Kinase (HPK-1) regulates stress responses and ageing in C. elegans |
title_fullStr | Homeodomain-Interacting Protein Kinase (HPK-1) regulates stress responses and ageing in C. elegans |
title_full_unstemmed | Homeodomain-Interacting Protein Kinase (HPK-1) regulates stress responses and ageing in C. elegans |
title_short | Homeodomain-Interacting Protein Kinase (HPK-1) regulates stress responses and ageing in C. elegans |
title_sort | homeodomain-interacting protein kinase (hpk-1) regulates stress responses and ageing in c. elegans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726358/ https://www.ncbi.nlm.nih.gov/pubmed/26791749 http://dx.doi.org/10.1038/srep19582 |
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