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A simple microfluidic platform to study age-dependent protein abundance and localization changes in Saccharomyces cerevisiae
The budding yeast Saccharomyces cerevisiae divides asymmetrically, with a smaller daughter cell emerging from its larger mother cell. While the daughter lineage is immortal, mother cells age with each cell division and have a finite lifespan. The replicative ageing of the yeast mother cell has been...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shared Science Publishers OG
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5425278/ https://www.ncbi.nlm.nih.gov/pubmed/28685142 http://dx.doi.org/10.15698/mic2017.05.573 |
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author | Cabrera, Margarita Novarina, Daniele Rempel, Irina L. Veenhoff, Liesbeth M. Chang, Michael |
author_facet | Cabrera, Margarita Novarina, Daniele Rempel, Irina L. Veenhoff, Liesbeth M. Chang, Michael |
author_sort | Cabrera, Margarita |
collection | PubMed |
description | The budding yeast Saccharomyces cerevisiae divides asymmetrically, with a smaller daughter cell emerging from its larger mother cell. While the daughter lineage is immortal, mother cells age with each cell division and have a finite lifespan. The replicative ageing of the yeast mother cell has been used as a model to study the ageing of mitotically active human cells. Several microfluidic platforms, which use fluid flow to selectively remove daughter cells, have recently been developed that can monitor cell physiology as mother cells age. However, these platforms are not trivial to set up and users often require many hours of training. In this study, we have developed a simple system, which combines a commercially available microfluidic platform (the CellASIC ONIX Microfluidic Platform) and a genetic tool to prevent the proliferation of daughter cells (the Mother Enrichment Program), to monitor protein abundance and localization changes during approximately the first half of the yeast replicative lifespan. We validated our system by observing known age-dependent changes, such as decreased Sir2 abundance, and have identified a protein with a previously unknown age-dependent change in localization. |
format | Online Article Text |
id | pubmed-5425278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Shared Science Publishers OG |
record_format | MEDLINE/PubMed |
spelling | pubmed-54252782017-07-06 A simple microfluidic platform to study age-dependent protein abundance and localization changes in Saccharomyces cerevisiae Cabrera, Margarita Novarina, Daniele Rempel, Irina L. Veenhoff, Liesbeth M. Chang, Michael Microb Cell Microbiology The budding yeast Saccharomyces cerevisiae divides asymmetrically, with a smaller daughter cell emerging from its larger mother cell. While the daughter lineage is immortal, mother cells age with each cell division and have a finite lifespan. The replicative ageing of the yeast mother cell has been used as a model to study the ageing of mitotically active human cells. Several microfluidic platforms, which use fluid flow to selectively remove daughter cells, have recently been developed that can monitor cell physiology as mother cells age. However, these platforms are not trivial to set up and users often require many hours of training. In this study, we have developed a simple system, which combines a commercially available microfluidic platform (the CellASIC ONIX Microfluidic Platform) and a genetic tool to prevent the proliferation of daughter cells (the Mother Enrichment Program), to monitor protein abundance and localization changes during approximately the first half of the yeast replicative lifespan. We validated our system by observing known age-dependent changes, such as decreased Sir2 abundance, and have identified a protein with a previously unknown age-dependent change in localization. Shared Science Publishers OG 2017-04-13 /pmc/articles/PMC5425278/ /pubmed/28685142 http://dx.doi.org/10.15698/mic2017.05.573 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged. |
spellingShingle | Microbiology Cabrera, Margarita Novarina, Daniele Rempel, Irina L. Veenhoff, Liesbeth M. Chang, Michael A simple microfluidic platform to study age-dependent protein abundance and localization changes in Saccharomyces cerevisiae |
title | A simple microfluidic platform to study age-dependent protein abundance and localization changes in Saccharomyces cerevisiae |
title_full | A simple microfluidic platform to study age-dependent protein abundance and localization changes in Saccharomyces cerevisiae |
title_fullStr | A simple microfluidic platform to study age-dependent protein abundance and localization changes in Saccharomyces cerevisiae |
title_full_unstemmed | A simple microfluidic platform to study age-dependent protein abundance and localization changes in Saccharomyces cerevisiae |
title_short | A simple microfluidic platform to study age-dependent protein abundance and localization changes in Saccharomyces cerevisiae |
title_sort | simple microfluidic platform to study age-dependent protein abundance and localization changes in saccharomyces cerevisiae |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5425278/ https://www.ncbi.nlm.nih.gov/pubmed/28685142 http://dx.doi.org/10.15698/mic2017.05.573 |
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