Cargando…
The protein kinase MBK-1 contributes to lifespan extension in daf-2 mutant and germline-deficient Caenorhabditis elegans
In Caenorhabditis elegans, reduction of insulin/IGF-1 like signaling and loss of germline stem cells both increase lifespan by activating the conserved transcription factor DAF-16 (FOXO). While the mechanisms that regulate DAF-16 nuclear localization in response to insulin/IGF-1 like signaling are w...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472741/ https://www.ncbi.nlm.nih.gov/pubmed/28562327 http://dx.doi.org/10.18632/aging.101244 |
_version_ | 1783244173207404544 |
---|---|
author | Mack, Hildegard I. D. Zhang, Peichuan Fonslow, Bryan R. Yates, John R. |
author_facet | Mack, Hildegard I. D. Zhang, Peichuan Fonslow, Bryan R. Yates, John R. |
author_sort | Mack, Hildegard I. D. |
collection | PubMed |
description | In Caenorhabditis elegans, reduction of insulin/IGF-1 like signaling and loss of germline stem cells both increase lifespan by activating the conserved transcription factor DAF-16 (FOXO). While the mechanisms that regulate DAF-16 nuclear localization in response to insulin/IGF-1 like signaling are well characterized, the molecular pathways that act in parallel to regulate DAF-16 transcriptional activity, and the pathways that couple DAF-16 activity to germline status, are not fully understood at present. Here, we report that inactivation of MBK-1, the C. elegans ortholog of the human FOXO1-kinase DYRK1A substantially shortens the prolonged lifespan of daf-2 and glp-1 mutant animals while decreasing wild-type lifespan to a lesser extent. On the other hand, lifespan-reduction by mutation of the MBK-1-related kinase HPK-1 was not preferential for long-lived mutants. Interestingly, mbk-1 loss still allowed for DAF-16 nuclear accumulation but reduced expression of certain DAF-16 target genes in germline-less, but not in daf-2 mutant animals. These findings indicate that mbk-1 and daf-16 functionally interact in the germline- but not in the daf-2 pathway. Together, our data suggest mbk-1 as a novel regulator of C. elegans longevity upon both, germline ablation and DAF-2 inhibition, and provide evidence for mbk-1 regulating DAF-16 activity in germline-deficient animals. |
format | Online Article Text |
id | pubmed-5472741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-54727412017-06-28 The protein kinase MBK-1 contributes to lifespan extension in daf-2 mutant and germline-deficient Caenorhabditis elegans Mack, Hildegard I. D. Zhang, Peichuan Fonslow, Bryan R. Yates, John R. Aging (Albany NY) Research Paper In Caenorhabditis elegans, reduction of insulin/IGF-1 like signaling and loss of germline stem cells both increase lifespan by activating the conserved transcription factor DAF-16 (FOXO). While the mechanisms that regulate DAF-16 nuclear localization in response to insulin/IGF-1 like signaling are well characterized, the molecular pathways that act in parallel to regulate DAF-16 transcriptional activity, and the pathways that couple DAF-16 activity to germline status, are not fully understood at present. Here, we report that inactivation of MBK-1, the C. elegans ortholog of the human FOXO1-kinase DYRK1A substantially shortens the prolonged lifespan of daf-2 and glp-1 mutant animals while decreasing wild-type lifespan to a lesser extent. On the other hand, lifespan-reduction by mutation of the MBK-1-related kinase HPK-1 was not preferential for long-lived mutants. Interestingly, mbk-1 loss still allowed for DAF-16 nuclear accumulation but reduced expression of certain DAF-16 target genes in germline-less, but not in daf-2 mutant animals. These findings indicate that mbk-1 and daf-16 functionally interact in the germline- but not in the daf-2 pathway. Together, our data suggest mbk-1 as a novel regulator of C. elegans longevity upon both, germline ablation and DAF-2 inhibition, and provide evidence for mbk-1 regulating DAF-16 activity in germline-deficient animals. Impact Journals LLC 2017-05-25 /pmc/articles/PMC5472741/ /pubmed/28562327 http://dx.doi.org/10.18632/aging.101244 Text en Copyright: © 2017 Mack et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Mack, Hildegard I. D. Zhang, Peichuan Fonslow, Bryan R. Yates, John R. The protein kinase MBK-1 contributes to lifespan extension in daf-2 mutant and germline-deficient Caenorhabditis elegans |
title | The protein kinase MBK-1 contributes to lifespan extension in daf-2 mutant and germline-deficient Caenorhabditis elegans |
title_full | The protein kinase MBK-1 contributes to lifespan extension in daf-2 mutant and germline-deficient Caenorhabditis elegans |
title_fullStr | The protein kinase MBK-1 contributes to lifespan extension in daf-2 mutant and germline-deficient Caenorhabditis elegans |
title_full_unstemmed | The protein kinase MBK-1 contributes to lifespan extension in daf-2 mutant and germline-deficient Caenorhabditis elegans |
title_short | The protein kinase MBK-1 contributes to lifespan extension in daf-2 mutant and germline-deficient Caenorhabditis elegans |
title_sort | protein kinase mbk-1 contributes to lifespan extension in daf-2 mutant and germline-deficient caenorhabditis elegans |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472741/ https://www.ncbi.nlm.nih.gov/pubmed/28562327 http://dx.doi.org/10.18632/aging.101244 |
work_keys_str_mv | AT mackhildegardid theproteinkinasembk1contributestolifespanextensionindaf2mutantandgermlinedeficientcaenorhabditiselegans AT zhangpeichuan theproteinkinasembk1contributestolifespanextensionindaf2mutantandgermlinedeficientcaenorhabditiselegans AT fonslowbryanr theproteinkinasembk1contributestolifespanextensionindaf2mutantandgermlinedeficientcaenorhabditiselegans AT yatesjohnr theproteinkinasembk1contributestolifespanextensionindaf2mutantandgermlinedeficientcaenorhabditiselegans AT mackhildegardid proteinkinasembk1contributestolifespanextensionindaf2mutantandgermlinedeficientcaenorhabditiselegans AT zhangpeichuan proteinkinasembk1contributestolifespanextensionindaf2mutantandgermlinedeficientcaenorhabditiselegans AT fonslowbryanr proteinkinasembk1contributestolifespanextensionindaf2mutantandgermlinedeficientcaenorhabditiselegans AT yatesjohnr proteinkinasembk1contributestolifespanextensionindaf2mutantandgermlinedeficientcaenorhabditiselegans |