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Isolation of intact RNA from cytometrically sorted Saccharomyces cerevisiae for the analysis of intrapopulation diversity of gene expression

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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  • Helmholtz-Zentrum für Umweltforschung (UFZ)

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OriginalspracheEnglisch
Seiten (von - bis)2203-11
Seitenumfang9
FachzeitschriftNature protocols
Jahrgang2
Ausgabenummer9
PublikationsstatusVeröffentlicht - 2007

Abstract

Characterizing and understanding the functional heterogeneity in a given population on the cellular and molecular level is a great challenge in microbiology. Each microorganism contributes differently to the overall performance of the community and responds differently to changing microenvironmental conditions. Here, we present a method for isolation of intact RNA out of small subpopulations of live Saccharomyces cerevisiae cells for differential gene expression analysis. The protocol includes fluorescence staining, flow cytometric analysis and sorting of live yeast cells, subsequent isolation of RNA from the resulting subpopulations and finally RNA quantification and integrity check. The isolated RNA can be transcribed into cDNA and successfully used for microarray analysis. This aids in relating molecular regulation processes within subpopulations with the dynamics and functioning of the entire population. The procedure can be accomplished in 2 d.

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Isolation of intact RNA from cytometrically sorted Saccharomyces cerevisiae for the analysis of intrapopulation diversity of gene expression. / Achilles, Jeannette; Stahl, Frank; Harms, Hauke et al.
in: Nature protocols, Jahrgang 2, Nr. 9, 2007, S. 2203-11.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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title = "Isolation of intact RNA from cytometrically sorted Saccharomyces cerevisiae for the analysis of intrapopulation diversity of gene expression",
abstract = "Characterizing and understanding the functional heterogeneity in a given population on the cellular and molecular level is a great challenge in microbiology. Each microorganism contributes differently to the overall performance of the community and responds differently to changing microenvironmental conditions. Here, we present a method for isolation of intact RNA out of small subpopulations of live Saccharomyces cerevisiae cells for differential gene expression analysis. The protocol includes fluorescence staining, flow cytometric analysis and sorting of live yeast cells, subsequent isolation of RNA from the resulting subpopulations and finally RNA quantification and integrity check. The isolated RNA can be transcribed into cDNA and successfully used for microarray analysis. This aids in relating molecular regulation processes within subpopulations with the dynamics and functioning of the entire population. The procedure can be accomplished in 2 d.",
keywords = "Flow Cytometry/methods, Gene Expression Profiling/methods, Genetic Variation, Oligonucleotide Array Sequence Analysis, RNA, Fungal/isolation & purification, Saccharomyces cerevisiae/genetics",
author = "Jeannette Achilles and Frank Stahl and Hauke Harms and Susann M{\"u}ller",
note = "Funding information: ACKNOWLEDGMENTS We thank H. Engewald and C. S{\"u}ring for technical assistance. We thank T. H{\"u}bschmann for technical assistance as well as for helpful discussions and A. Pernthaler for critical reading of the manuscript. We also thank C. Repenning and M. P{\"a}hler from the working group {\textquoteleft}Chip Technology{\textquoteright} at the Institute of Technical Chemistry of the University of Hannover. This work was supported by the Deutsche Forschungsgemeinschaft (MU 1089/5-3).",
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doi = "10.1038/nprot.2007.322",
language = "English",
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journal = "Nature protocols",
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Download

TY - JOUR

T1 - Isolation of intact RNA from cytometrically sorted Saccharomyces cerevisiae for the analysis of intrapopulation diversity of gene expression

AU - Achilles, Jeannette

AU - Stahl, Frank

AU - Harms, Hauke

AU - Müller, Susann

N1 - Funding information: ACKNOWLEDGMENTS We thank H. Engewald and C. Süring for technical assistance. We thank T. Hübschmann for technical assistance as well as for helpful discussions and A. Pernthaler for critical reading of the manuscript. We also thank C. Repenning and M. Pähler from the working group ‘Chip Technology’ at the Institute of Technical Chemistry of the University of Hannover. This work was supported by the Deutsche Forschungsgemeinschaft (MU 1089/5-3).

PY - 2007

Y1 - 2007

N2 - Characterizing and understanding the functional heterogeneity in a given population on the cellular and molecular level is a great challenge in microbiology. Each microorganism contributes differently to the overall performance of the community and responds differently to changing microenvironmental conditions. Here, we present a method for isolation of intact RNA out of small subpopulations of live Saccharomyces cerevisiae cells for differential gene expression analysis. The protocol includes fluorescence staining, flow cytometric analysis and sorting of live yeast cells, subsequent isolation of RNA from the resulting subpopulations and finally RNA quantification and integrity check. The isolated RNA can be transcribed into cDNA and successfully used for microarray analysis. This aids in relating molecular regulation processes within subpopulations with the dynamics and functioning of the entire population. The procedure can be accomplished in 2 d.

AB - Characterizing and understanding the functional heterogeneity in a given population on the cellular and molecular level is a great challenge in microbiology. Each microorganism contributes differently to the overall performance of the community and responds differently to changing microenvironmental conditions. Here, we present a method for isolation of intact RNA out of small subpopulations of live Saccharomyces cerevisiae cells for differential gene expression analysis. The protocol includes fluorescence staining, flow cytometric analysis and sorting of live yeast cells, subsequent isolation of RNA from the resulting subpopulations and finally RNA quantification and integrity check. The isolated RNA can be transcribed into cDNA and successfully used for microarray analysis. This aids in relating molecular regulation processes within subpopulations with the dynamics and functioning of the entire population. The procedure can be accomplished in 2 d.

KW - Flow Cytometry/methods

KW - Gene Expression Profiling/methods

KW - Genetic Variation

KW - Oligonucleotide Array Sequence Analysis

KW - RNA, Fungal/isolation & purification

KW - Saccharomyces cerevisiae/genetics

U2 - 10.1038/nprot.2007.322

DO - 10.1038/nprot.2007.322

M3 - Article

C2 - 17853877

VL - 2

SP - 2203

EP - 2211

JO - Nature protocols

JF - Nature protocols

SN - 1750-2799

IS - 9

ER -

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