Loading…
Quantitative characterization of cell synchronization in yeast
Metabolic oscillations in baker's yeast serve as a model system for synchronization of biochemical oscillations. Despite widespread interest, the complexity of the phenomenon has been an obstacle for a quantitative understanding of the cell synchronization process. In particular, when two yeast...
Saved in:
Published in: | Proceedings of the National Academy of Sciences - PNAS 2007-07, Vol.104 (31), p.12732-12736 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c620t-c6dfdbdf65cead56292fb97b0dff14509d1449135464e66ff1a7c6e1535bda473 |
---|---|
cites | cdi_FETCH-LOGICAL-c620t-c6dfdbdf65cead56292fb97b0dff14509d1449135464e66ff1a7c6e1535bda473 |
container_end_page | 12736 |
container_issue | 31 |
container_start_page | 12732 |
container_title | Proceedings of the National Academy of Sciences - PNAS |
container_volume | 104 |
creator | Danø, Sune Madsen, Mads Find Sørensen, Preben Graae |
description | Metabolic oscillations in baker's yeast serve as a model system for synchronization of biochemical oscillations. Despite widespread interest, the complexity of the phenomenon has been an obstacle for a quantitative understanding of the cell synchronization process. In particular, when two yeast cell populations oscillating 180° out of phase are mixed, it appears as if the synchronization dynamics is too fast to be explained. We have probed the synchronization dynamics by forcing experiments in an open-flow reactor, and we find that acetaldehyde has a very strong synchronization effect that can account quantitatively for the classical mixing experiment. The fast synchronization dynamics is explained by a general synchronization mechanism, which is dominated by a fast amplitude response as opposed to the expected slow phase change. We also show that glucose can mediate this kind of synchronization, provided that the glucose transporter is not saturated. This makes the phenomenon potentially relevant for a broad range of cell types. |
doi_str_mv | 10.1073/pnas.0702560104 |
format | article |
fullrecord | <record><control><sourceid>jstor_proqu</sourceid><recordid>TN_cdi_proquest_journals_201311343</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>25436373</jstor_id><sourcerecordid>25436373</sourcerecordid><originalsourceid>FETCH-LOGICAL-c620t-c6dfdbdf65cead56292fb97b0dff14509d1449135464e66ff1a7c6e1535bda473</originalsourceid><addsrcrecordid>eNqFkc2LFDEQxYMo7rh69qQ2HgQPs1uVz85lQRa_YEFE9xzS3clODz2dMUkvjn-9aWbcUS97SaDqV4969Qh5jnCGoNj5drTpDBRQIQGBPyALBI1LyTU8JAsAqpY1p_yEPElpDQBa1PCYnKCSggrUC3LxdbJj7rPN_a2r2pWNts0u9r9KIYxV8FXrhqFKu7FdxTD-qfdjtXM25afkkbdDcs8O_ym5_vD---Wn5dWXj58v310tW0khl7fzXdN5KVpnOyGppr7RqoHOe-QCdIeca2SCS-6kLEWrWulQMNF0lit2Si72utup2biudWOOdjDb2G9s3Jlge_NvZ-xX5ibcGtRMFZUi8OYgEMOPyaVsNn2ardnRhSkZWSMKzut7QVpuCjXnBXz9H7gOUxzLFQqDDJFxVqDzPdTGkFJ0_m5lBDMnaOYEzTHBMvHyb6dH_hBZAd4egHnyKMcNQ4NUMWr8NAzZ_cyFre5hC_Jij6xTDvGOoYIzydTs4NW-720w9ib2yVx_mw0CKM01Q_YbKJPDgA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>201311343</pqid></control><display><type>article</type><title>Quantitative characterization of cell synchronization in yeast</title><source>PubMed Central(OpenAccess)</source><source>JSTOR Archival Journals and Primary Sources Collection</source><creator>Danø, Sune ; Madsen, Mads Find ; Sørensen, Preben Graae</creator><creatorcontrib>Danø, Sune ; Madsen, Mads Find ; Sørensen, Preben Graae</creatorcontrib><description>Metabolic oscillations in baker's yeast serve as a model system for synchronization of biochemical oscillations. Despite widespread interest, the complexity of the phenomenon has been an obstacle for a quantitative understanding of the cell synchronization process. In particular, when two yeast cell populations oscillating 180° out of phase are mixed, it appears as if the synchronization dynamics is too fast to be explained. We have probed the synchronization dynamics by forcing experiments in an open-flow reactor, and we find that acetaldehyde has a very strong synchronization effect that can account quantitatively for the classical mixing experiment. The fast synchronization dynamics is explained by a general synchronization mechanism, which is dominated by a fast amplitude response as opposed to the expected slow phase change. We also show that glucose can mediate this kind of synchronization, provided that the glucose transporter is not saturated. This makes the phenomenon potentially relevant for a broad range of cell types.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0702560104</identifier><identifier>PMID: 17652519</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>acetaldehyde ; Acetaldehyde - pharmacology ; Biological Clocks - physiology ; Biological Sciences ; Biophysics ; bioreactors ; cell culture ; cell synchronization ; Cells ; continuous-flow stirred-tank reactor ; Cyanides ; Facilitative glucose transport proteins ; Fluorescence ; glucose ; Glucose - metabolism ; Glycolysis ; microbial growth ; microbial physiology ; Multiphase flow ; nutrient availability ; Oscillators ; Phase shift ; Resonance ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - cytology ; Saccharomyces cerevisiae - drug effects ; Synchronizers ; Temperature ; Yeast ; Yeasts</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2007-07, Vol.104 (31), p.12732-12736</ispartof><rights>Copyright 2007 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Jul 31, 2007</rights><rights>2007 by The National Academy of Sciences of the USA 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c620t-c6dfdbdf65cead56292fb97b0dff14509d1449135464e66ff1a7c6e1535bda473</citedby><cites>FETCH-LOGICAL-c620t-c6dfdbdf65cead56292fb97b0dff14509d1449135464e66ff1a7c6e1535bda473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/104/31.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/25436373$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/25436373$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17652519$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Danø, Sune</creatorcontrib><creatorcontrib>Madsen, Mads Find</creatorcontrib><creatorcontrib>Sørensen, Preben Graae</creatorcontrib><title>Quantitative characterization of cell synchronization in yeast</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Metabolic oscillations in baker's yeast serve as a model system for synchronization of biochemical oscillations. Despite widespread interest, the complexity of the phenomenon has been an obstacle for a quantitative understanding of the cell synchronization process. In particular, when two yeast cell populations oscillating 180° out of phase are mixed, it appears as if the synchronization dynamics is too fast to be explained. We have probed the synchronization dynamics by forcing experiments in an open-flow reactor, and we find that acetaldehyde has a very strong synchronization effect that can account quantitatively for the classical mixing experiment. The fast synchronization dynamics is explained by a general synchronization mechanism, which is dominated by a fast amplitude response as opposed to the expected slow phase change. We also show that glucose can mediate this kind of synchronization, provided that the glucose transporter is not saturated. This makes the phenomenon potentially relevant for a broad range of cell types.</description><subject>acetaldehyde</subject><subject>Acetaldehyde - pharmacology</subject><subject>Biological Clocks - physiology</subject><subject>Biological Sciences</subject><subject>Biophysics</subject><subject>bioreactors</subject><subject>cell culture</subject><subject>cell synchronization</subject><subject>Cells</subject><subject>continuous-flow stirred-tank reactor</subject><subject>Cyanides</subject><subject>Facilitative glucose transport proteins</subject><subject>Fluorescence</subject><subject>glucose</subject><subject>Glucose - metabolism</subject><subject>Glycolysis</subject><subject>microbial growth</subject><subject>microbial physiology</subject><subject>Multiphase flow</subject><subject>nutrient availability</subject><subject>Oscillators</subject><subject>Phase shift</subject><subject>Resonance</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - cytology</subject><subject>Saccharomyces cerevisiae - drug effects</subject><subject>Synchronizers</subject><subject>Temperature</subject><subject>Yeast</subject><subject>Yeasts</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkc2LFDEQxYMo7rh69qQ2HgQPs1uVz85lQRa_YEFE9xzS3clODz2dMUkvjn-9aWbcUS97SaDqV4969Qh5jnCGoNj5drTpDBRQIQGBPyALBI1LyTU8JAsAqpY1p_yEPElpDQBa1PCYnKCSggrUC3LxdbJj7rPN_a2r2pWNts0u9r9KIYxV8FXrhqFKu7FdxTD-qfdjtXM25afkkbdDcs8O_ym5_vD---Wn5dWXj58v310tW0khl7fzXdN5KVpnOyGppr7RqoHOe-QCdIeca2SCS-6kLEWrWulQMNF0lit2Si72utup2biudWOOdjDb2G9s3Jlge_NvZ-xX5ibcGtRMFZUi8OYgEMOPyaVsNn2ardnRhSkZWSMKzut7QVpuCjXnBXz9H7gOUxzLFQqDDJFxVqDzPdTGkFJ0_m5lBDMnaOYEzTHBMvHyb6dH_hBZAd4egHnyKMcNQ4NUMWr8NAzZ_cyFre5hC_Jij6xTDvGOoYIzydTs4NW-720w9ib2yVx_mw0CKM01Q_YbKJPDgA</recordid><startdate>20070731</startdate><enddate>20070731</enddate><creator>Danø, Sune</creator><creator>Madsen, Mads Find</creator><creator>Sørensen, Preben Graae</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20070731</creationdate><title>Quantitative characterization of cell synchronization in yeast</title><author>Danø, Sune ; Madsen, Mads Find ; Sørensen, Preben Graae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c620t-c6dfdbdf65cead56292fb97b0dff14509d1449135464e66ff1a7c6e1535bda473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>acetaldehyde</topic><topic>Acetaldehyde - pharmacology</topic><topic>Biological Clocks - physiology</topic><topic>Biological Sciences</topic><topic>Biophysics</topic><topic>bioreactors</topic><topic>cell culture</topic><topic>cell synchronization</topic><topic>Cells</topic><topic>continuous-flow stirred-tank reactor</topic><topic>Cyanides</topic><topic>Facilitative glucose transport proteins</topic><topic>Fluorescence</topic><topic>glucose</topic><topic>Glucose - metabolism</topic><topic>Glycolysis</topic><topic>microbial growth</topic><topic>microbial physiology</topic><topic>Multiphase flow</topic><topic>nutrient availability</topic><topic>Oscillators</topic><topic>Phase shift</topic><topic>Resonance</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - cytology</topic><topic>Saccharomyces cerevisiae - drug effects</topic><topic>Synchronizers</topic><topic>Temperature</topic><topic>Yeast</topic><topic>Yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Danø, Sune</creatorcontrib><creatorcontrib>Madsen, Mads Find</creatorcontrib><creatorcontrib>Sørensen, Preben Graae</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Danø, Sune</au><au>Madsen, Mads Find</au><au>Sørensen, Preben Graae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative characterization of cell synchronization in yeast</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2007-07-31</date><risdate>2007</risdate><volume>104</volume><issue>31</issue><spage>12732</spage><epage>12736</epage><pages>12732-12736</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Metabolic oscillations in baker's yeast serve as a model system for synchronization of biochemical oscillations. Despite widespread interest, the complexity of the phenomenon has been an obstacle for a quantitative understanding of the cell synchronization process. In particular, when two yeast cell populations oscillating 180° out of phase are mixed, it appears as if the synchronization dynamics is too fast to be explained. We have probed the synchronization dynamics by forcing experiments in an open-flow reactor, and we find that acetaldehyde has a very strong synchronization effect that can account quantitatively for the classical mixing experiment. The fast synchronization dynamics is explained by a general synchronization mechanism, which is dominated by a fast amplitude response as opposed to the expected slow phase change. We also show that glucose can mediate this kind of synchronization, provided that the glucose transporter is not saturated. This makes the phenomenon potentially relevant for a broad range of cell types.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>17652519</pmid><doi>10.1073/pnas.0702560104</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0027-8424 |
ispartof | Proceedings of the National Academy of Sciences - PNAS, 2007-07, Vol.104 (31), p.12732-12736 |
issn | 0027-8424 1091-6490 |
language | eng |
recordid | cdi_proquest_journals_201311343 |
source | PubMed Central(OpenAccess); JSTOR Archival Journals and Primary Sources Collection |
subjects | acetaldehyde Acetaldehyde - pharmacology Biological Clocks - physiology Biological Sciences Biophysics bioreactors cell culture cell synchronization Cells continuous-flow stirred-tank reactor Cyanides Facilitative glucose transport proteins Fluorescence glucose Glucose - metabolism Glycolysis microbial growth microbial physiology Multiphase flow nutrient availability Oscillators Phase shift Resonance Saccharomyces cerevisiae Saccharomyces cerevisiae - cytology Saccharomyces cerevisiae - drug effects Synchronizers Temperature Yeast Yeasts |
title | Quantitative characterization of cell synchronization in yeast |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T06%3A33%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Quantitative%20characterization%20of%20cell%20synchronization%20in%20yeast&rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20-%20PNAS&rft.au=Dan%C3%B8,%20Sune&rft.date=2007-07-31&rft.volume=104&rft.issue=31&rft.spage=12732&rft.epage=12736&rft.pages=12732-12736&rft.issn=0027-8424&rft.eissn=1091-6490&rft_id=info:doi/10.1073/pnas.0702560104&rft_dat=%3Cjstor_proqu%3E25436373%3C/jstor_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c620t-c6dfdbdf65cead56292fb97b0dff14509d1449135464e66ff1a7c6e1535bda473%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=201311343&rft_id=info:pmid/17652519&rft_jstor_id=25436373&rfr_iscdi=true |