Transcriptome Remodeling of Differentiated Cells during Chronological Ageing of Yeast Colonies: New Insights into Metabolic Differentiation

We present the spatiotemporal metabolic differentiation of yeast cell subpopulations from upper, lower, and margin regions of colonies of different ages, based on comprehensive transcriptomic analysis. Furthermore, the analysis was extended to include smaller cell subpopulations identified previousl...

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Main Authors: Derek Wilkinson, Jana Maršíková, Otakar Hlaváček, Gregor D. Gilfillan, Eva Ježková, Ragnhild Aaløkken, Libuše Váchová, Zdena Palková
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Oxidative Medicine and Cellular Longevity
Online Access:http://dx.doi.org/10.1155/2018/4932905
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spelling doaj-9405615d2aba4f1d98c0d40c68f57cc42020-11-25T02:21:03ZengHindawi LimitedOxidative Medicine and Cellular Longevity1942-09001942-09942018-01-01201810.1155/2018/49329054932905Transcriptome Remodeling of Differentiated Cells during Chronological Ageing of Yeast Colonies: New Insights into Metabolic DifferentiationDerek Wilkinson0Jana Maršíková1Otakar Hlaváček2Gregor D. Gilfillan3Eva Ježková4Ragnhild Aaløkken5Libuše Váchová6Zdena Palková7Faculty of Science, Charles University, BIOCEV, 252 50 Vestec, Czech RepublicFaculty of Science, Charles University, BIOCEV, 252 50 Vestec, Czech RepublicInstitute of Microbiology of the Czech Academy of Sciences, BIOCEV, 252 50 Vestec, Czech RepublicDepartment of Medical Genetics, Oslo University Hospital and University of Oslo, 0450 Oslo, NorwayFaculty of Science, Charles University, BIOCEV, 252 50 Vestec, Czech RepublicDepartment of Medical Genetics, Oslo University Hospital and University of Oslo, 0450 Oslo, NorwayInstitute of Microbiology of the Czech Academy of Sciences, BIOCEV, 252 50 Vestec, Czech RepublicFaculty of Science, Charles University, BIOCEV, 252 50 Vestec, Czech RepublicWe present the spatiotemporal metabolic differentiation of yeast cell subpopulations from upper, lower, and margin regions of colonies of different ages, based on comprehensive transcriptomic analysis. Furthermore, the analysis was extended to include smaller cell subpopulations identified previously by microscopy within fully differentiated U and L cells of aged colonies. New data from RNA-seq provides both spatial and temporal information on cell metabolic reprogramming during colony ageing and shows that cells at marginal positions are similar to upper cells, but both these cell types are metabolically distinct from cells localized to lower colony regions. As colonies age, dramatic metabolic reprogramming occurs in cells of upper regions, while changes in margin and lower cells are less prominent. Interestingly, whereas clear expression differences were identified between two L cell subpopulations, U cells (which adopt metabolic profiles, similar to those of tumor cells) form a more homogeneous cell population. The data identified crucial metabolic reprogramming events that arise de novo during colony ageing and are linked to U and L cell colony differentiation and support a role for mitochondria in this differentiation process.http://dx.doi.org/10.1155/2018/4932905
collection DOAJ
language English
format Article
sources DOAJ
author Derek Wilkinson
Jana Maršíková
Otakar Hlaváček
Gregor D. Gilfillan
Eva Ježková
Ragnhild Aaløkken
Libuše Váchová
Zdena Palková
spellingShingle Derek Wilkinson
Jana Maršíková
Otakar Hlaváček
Gregor D. Gilfillan
Eva Ježková
Ragnhild Aaløkken
Libuše Váchová
Zdena Palková
Transcriptome Remodeling of Differentiated Cells during Chronological Ageing of Yeast Colonies: New Insights into Metabolic Differentiation
Oxidative Medicine and Cellular Longevity
author_facet Derek Wilkinson
Jana Maršíková
Otakar Hlaváček
Gregor D. Gilfillan
Eva Ježková
Ragnhild Aaløkken
Libuše Váchová
Zdena Palková
author_sort Derek Wilkinson
title Transcriptome Remodeling of Differentiated Cells during Chronological Ageing of Yeast Colonies: New Insights into Metabolic Differentiation
title_short Transcriptome Remodeling of Differentiated Cells during Chronological Ageing of Yeast Colonies: New Insights into Metabolic Differentiation
title_full Transcriptome Remodeling of Differentiated Cells during Chronological Ageing of Yeast Colonies: New Insights into Metabolic Differentiation
title_fullStr Transcriptome Remodeling of Differentiated Cells during Chronological Ageing of Yeast Colonies: New Insights into Metabolic Differentiation
title_full_unstemmed Transcriptome Remodeling of Differentiated Cells during Chronological Ageing of Yeast Colonies: New Insights into Metabolic Differentiation
title_sort transcriptome remodeling of differentiated cells during chronological ageing of yeast colonies: new insights into metabolic differentiation
publisher Hindawi Limited
series Oxidative Medicine and Cellular Longevity
issn 1942-0900
1942-0994
publishDate 2018-01-01
description We present the spatiotemporal metabolic differentiation of yeast cell subpopulations from upper, lower, and margin regions of colonies of different ages, based on comprehensive transcriptomic analysis. Furthermore, the analysis was extended to include smaller cell subpopulations identified previously by microscopy within fully differentiated U and L cells of aged colonies. New data from RNA-seq provides both spatial and temporal information on cell metabolic reprogramming during colony ageing and shows that cells at marginal positions are similar to upper cells, but both these cell types are metabolically distinct from cells localized to lower colony regions. As colonies age, dramatic metabolic reprogramming occurs in cells of upper regions, while changes in margin and lower cells are less prominent. Interestingly, whereas clear expression differences were identified between two L cell subpopulations, U cells (which adopt metabolic profiles, similar to those of tumor cells) form a more homogeneous cell population. The data identified crucial metabolic reprogramming events that arise de novo during colony ageing and are linked to U and L cell colony differentiation and support a role for mitochondria in this differentiation process.
url http://dx.doi.org/10.1155/2018/4932905
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