Loading…
Gcn5 and Rpd3 have a limited role in the regulation of cell cycle transcripts during the G1 and S phases in Saccharomyces cerevisiae
Activation of cell cycle regulated transcription during the G1-to-S transition initiates S phase entry and cell cycle commitment. The molecular mechanisms involving G1/S transcriptional regulation are well established and have been shown to be evolutionary conserved from yeast to humans. Previous wo...
Saved in:
Published in: | Scientific reports 2019-07, Vol.9 (1), p.10686-9, Article 10686 |
---|---|
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-c511t-b183571563db0360ff24615e2daed0218ac9b9349b33d4cbd42d9beb884028e53 |
---|---|
cites | cdi_FETCH-LOGICAL-c511t-b183571563db0360ff24615e2daed0218ac9b9349b33d4cbd42d9beb884028e53 |
container_end_page | 9 |
container_issue | 1 |
container_start_page | 10686 |
container_title | Scientific reports |
container_volume | 9 |
creator | Kishkevich, A. Cooke, S. L. Harris, M. R. A. de Bruin, R. A. M. |
description | Activation of cell cycle regulated transcription during the G1-to-S transition initiates S phase entry and cell cycle commitment. The molecular mechanisms involving G1/S transcriptional regulation are well established and have been shown to be evolutionary conserved from yeast to humans. Previous work has suggested that changes to the chromatin state, specifically through histone acetylation, has an important role in the regulation of G1/S transcription in both yeast and human cells. Here we investigate the role of histone acetylation in G1/S transcriptional regulation in the budding yeast
Saccharomyces cerevisiae
. Our work shows that histone acetylation at specific sites at G1/S target gene promoters peaks at the G1-to-S transition, coinciding with their peak transcription levels. Acetylation at G1/S target promoters is significantly reduced upon deletion of the previously implicated histone acetyltransferase Gcn5, but G1/S cell cycle regulated transcription is largely unaffected. The histone deacetylase Rpd3, suggested to have a role in Whi5-dependent repression, is required for full repression of G1/S target genes in the G1 and S phases. However, in the context of transcriptionally active levels during the G1-to-S transition, this seems to play a minor role in the regulation of cell cycle transcription. Our data suggests that histone acetylation might modulate the amplitude of G1/S cell cycle regulated transcription in
Saccharomyces cerevisiae
, but has a limited role in its overall regulation. |
doi_str_mv | 10.1038/s41598-019-47170-z |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6650506</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2297179590</sourcerecordid><originalsourceid>FETCH-LOGICAL-c511t-b183571563db0360ff24615e2daed0218ac9b9349b33d4cbd42d9beb884028e53</originalsourceid><addsrcrecordid>eNp9kctu1DAUhi0EolXpC7BAltiwSfE1E2-QUFWGSpWQKKwtxz6ZuErsYCcjTdc8OJ6ZUgoLvLHl853_XH6EXlNyQQlv3mdBpWoqQlUlVnRFqvtn6JQRISvGGXv-5H2CznO-I-VIpgRVL9EJp5yvmpqcop9rGyQ2weGvk-O4N1vABg9-9DM4nOIA2Ac894ATbJbBzD4GHDtsYRiw3dkSn5MJ2SY_zRm7JfmwOfBrepC9xVNvMuS9zK2xtjcpjjtbPiwk2PrsDbxCLzozZDh_uM_Q909X3y4_Vzdf1teXH28qKymdq5Y2XK6orLlrCa9J1zFRUwnMGXCE0cZY1SouVMu5E7Z1gjnVQts0grAGJD9DH46609KO4CyE0vugp-RHk3Y6Gq__jgTf603c6rqWRJK6CLx7EEjxxwJ51qPP-1WYAHHJmrGac8bLlgv69h_0Li4plPEKpYpjSipSKHakbIo5J-gem6FE733WR5918VkffNb3JenN0zEeU367WgB-BPK0twPSn9r_kf0FBvm0Uw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2297179590</pqid></control><display><type>article</type><title>Gcn5 and Rpd3 have a limited role in the regulation of cell cycle transcripts during the G1 and S phases in Saccharomyces cerevisiae</title><source>PMC (PubMed Central)</source><source>Full-Text Journals in Chemistry (Open access)</source><source>Publicly Available Content (ProQuest)</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Kishkevich, A. ; Cooke, S. L. ; Harris, M. R. A. ; de Bruin, R. A. M.</creator><creatorcontrib>Kishkevich, A. ; Cooke, S. L. ; Harris, M. R. A. ; de Bruin, R. A. M.</creatorcontrib><description>Activation of cell cycle regulated transcription during the G1-to-S transition initiates S phase entry and cell cycle commitment. The molecular mechanisms involving G1/S transcriptional regulation are well established and have been shown to be evolutionary conserved from yeast to humans. Previous work has suggested that changes to the chromatin state, specifically through histone acetylation, has an important role in the regulation of G1/S transcription in both yeast and human cells. Here we investigate the role of histone acetylation in G1/S transcriptional regulation in the budding yeast
Saccharomyces cerevisiae
. Our work shows that histone acetylation at specific sites at G1/S target gene promoters peaks at the G1-to-S transition, coinciding with their peak transcription levels. Acetylation at G1/S target promoters is significantly reduced upon deletion of the previously implicated histone acetyltransferase Gcn5, but G1/S cell cycle regulated transcription is largely unaffected. The histone deacetylase Rpd3, suggested to have a role in Whi5-dependent repression, is required for full repression of G1/S target genes in the G1 and S phases. However, in the context of transcriptionally active levels during the G1-to-S transition, this seems to play a minor role in the regulation of cell cycle transcription. Our data suggests that histone acetylation might modulate the amplitude of G1/S cell cycle regulated transcription in
Saccharomyces cerevisiae
, but has a limited role in its overall regulation.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-019-47170-z</identifier><identifier>PMID: 31337860</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>38/22 ; 38/77 ; 631/337/572 ; 631/80/641/2350 ; Acetylation ; Cell activation ; Cell cycle ; Cell Cycle - physiology ; Cell Cycle Proteins - genetics ; Cell Cycle Proteins - metabolism ; Chromatin ; Clonal deletion ; Evolutionary conservation ; Gene deletion ; Gene Expression Regulation, Fungal ; Gene regulation ; Histone acetyltransferase ; Histone Acetyltransferases - genetics ; Histone Acetyltransferases - metabolism ; Histone deacetylase ; Histone Deacetylases - genetics ; Histone Deacetylases - metabolism ; Humanities and Social Sciences ; Molecular modelling ; multidisciplinary ; Promoter Regions, Genetic ; Promoters ; S phase ; S Phase - physiology ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae Proteins - genetics ; Saccharomyces cerevisiae Proteins - metabolism ; Science ; Science (multidisciplinary) ; Transcription ; Yeast ; Yeasts</subject><ispartof>Scientific reports, 2019-07, Vol.9 (1), p.10686-9, Article 10686</ispartof><rights>The Author(s) 2019</rights><rights>2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-b183571563db0360ff24615e2daed0218ac9b9349b33d4cbd42d9beb884028e53</citedby><cites>FETCH-LOGICAL-c511t-b183571563db0360ff24615e2daed0218ac9b9349b33d4cbd42d9beb884028e53</cites><orcidid>0000-0001-8169-8735 ; 0000-0002-2290-9675</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2297179590/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2297179590?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31337860$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kishkevich, A.</creatorcontrib><creatorcontrib>Cooke, S. L.</creatorcontrib><creatorcontrib>Harris, M. R. A.</creatorcontrib><creatorcontrib>de Bruin, R. A. M.</creatorcontrib><title>Gcn5 and Rpd3 have a limited role in the regulation of cell cycle transcripts during the G1 and S phases in Saccharomyces cerevisiae</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Activation of cell cycle regulated transcription during the G1-to-S transition initiates S phase entry and cell cycle commitment. The molecular mechanisms involving G1/S transcriptional regulation are well established and have been shown to be evolutionary conserved from yeast to humans. Previous work has suggested that changes to the chromatin state, specifically through histone acetylation, has an important role in the regulation of G1/S transcription in both yeast and human cells. Here we investigate the role of histone acetylation in G1/S transcriptional regulation in the budding yeast
Saccharomyces cerevisiae
. Our work shows that histone acetylation at specific sites at G1/S target gene promoters peaks at the G1-to-S transition, coinciding with their peak transcription levels. Acetylation at G1/S target promoters is significantly reduced upon deletion of the previously implicated histone acetyltransferase Gcn5, but G1/S cell cycle regulated transcription is largely unaffected. The histone deacetylase Rpd3, suggested to have a role in Whi5-dependent repression, is required for full repression of G1/S target genes in the G1 and S phases. However, in the context of transcriptionally active levels during the G1-to-S transition, this seems to play a minor role in the regulation of cell cycle transcription. Our data suggests that histone acetylation might modulate the amplitude of G1/S cell cycle regulated transcription in
Saccharomyces cerevisiae
, but has a limited role in its overall regulation.</description><subject>38/22</subject><subject>38/77</subject><subject>631/337/572</subject><subject>631/80/641/2350</subject><subject>Acetylation</subject><subject>Cell activation</subject><subject>Cell cycle</subject><subject>Cell Cycle - physiology</subject><subject>Cell Cycle Proteins - genetics</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Chromatin</subject><subject>Clonal deletion</subject><subject>Evolutionary conservation</subject><subject>Gene deletion</subject><subject>Gene Expression Regulation, Fungal</subject><subject>Gene regulation</subject><subject>Histone acetyltransferase</subject><subject>Histone Acetyltransferases - genetics</subject><subject>Histone Acetyltransferases - metabolism</subject><subject>Histone deacetylase</subject><subject>Histone Deacetylases - genetics</subject><subject>Histone Deacetylases - metabolism</subject><subject>Humanities and Social Sciences</subject><subject>Molecular modelling</subject><subject>multidisciplinary</subject><subject>Promoter Regions, Genetic</subject><subject>Promoters</subject><subject>S phase</subject><subject>S Phase - physiology</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae Proteins - genetics</subject><subject>Saccharomyces cerevisiae Proteins - metabolism</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Transcription</subject><subject>Yeast</subject><subject>Yeasts</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9kctu1DAUhi0EolXpC7BAltiwSfE1E2-QUFWGSpWQKKwtxz6ZuErsYCcjTdc8OJ6ZUgoLvLHl853_XH6EXlNyQQlv3mdBpWoqQlUlVnRFqvtn6JQRISvGGXv-5H2CznO-I-VIpgRVL9EJp5yvmpqcop9rGyQ2weGvk-O4N1vABg9-9DM4nOIA2Ac894ATbJbBzD4GHDtsYRiw3dkSn5MJ2SY_zRm7JfmwOfBrepC9xVNvMuS9zK2xtjcpjjtbPiwk2PrsDbxCLzozZDh_uM_Q909X3y4_Vzdf1teXH28qKymdq5Y2XK6orLlrCa9J1zFRUwnMGXCE0cZY1SouVMu5E7Z1gjnVQts0grAGJD9DH46609KO4CyE0vugp-RHk3Y6Gq__jgTf603c6rqWRJK6CLx7EEjxxwJ51qPP-1WYAHHJmrGac8bLlgv69h_0Li4plPEKpYpjSipSKHakbIo5J-gem6FE733WR5918VkffNb3JenN0zEeU367WgB-BPK0twPSn9r_kf0FBvm0Uw</recordid><startdate>20190723</startdate><enddate>20190723</enddate><creator>Kishkevich, A.</creator><creator>Cooke, S. L.</creator><creator>Harris, M. R. A.</creator><creator>de Bruin, R. A. M.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8169-8735</orcidid><orcidid>https://orcid.org/0000-0002-2290-9675</orcidid></search><sort><creationdate>20190723</creationdate><title>Gcn5 and Rpd3 have a limited role in the regulation of cell cycle transcripts during the G1 and S phases in Saccharomyces cerevisiae</title><author>Kishkevich, A. ; Cooke, S. L. ; Harris, M. R. A. ; de Bruin, R. A. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-b183571563db0360ff24615e2daed0218ac9b9349b33d4cbd42d9beb884028e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>38/22</topic><topic>38/77</topic><topic>631/337/572</topic><topic>631/80/641/2350</topic><topic>Acetylation</topic><topic>Cell activation</topic><topic>Cell cycle</topic><topic>Cell Cycle - physiology</topic><topic>Cell Cycle Proteins - genetics</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Chromatin</topic><topic>Clonal deletion</topic><topic>Evolutionary conservation</topic><topic>Gene deletion</topic><topic>Gene Expression Regulation, Fungal</topic><topic>Gene regulation</topic><topic>Histone acetyltransferase</topic><topic>Histone Acetyltransferases - genetics</topic><topic>Histone Acetyltransferases - metabolism</topic><topic>Histone deacetylase</topic><topic>Histone Deacetylases - genetics</topic><topic>Histone Deacetylases - metabolism</topic><topic>Humanities and Social Sciences</topic><topic>Molecular modelling</topic><topic>multidisciplinary</topic><topic>Promoter Regions, Genetic</topic><topic>Promoters</topic><topic>S phase</topic><topic>S Phase - physiology</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae Proteins - genetics</topic><topic>Saccharomyces cerevisiae Proteins - metabolism</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Transcription</topic><topic>Yeast</topic><topic>Yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kishkevich, A.</creatorcontrib><creatorcontrib>Cooke, S. L.</creatorcontrib><creatorcontrib>Harris, M. R. A.</creatorcontrib><creatorcontrib>de Bruin, R. A. M.</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kishkevich, A.</au><au>Cooke, S. L.</au><au>Harris, M. R. A.</au><au>de Bruin, R. A. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gcn5 and Rpd3 have a limited role in the regulation of cell cycle transcripts during the G1 and S phases in Saccharomyces cerevisiae</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2019-07-23</date><risdate>2019</risdate><volume>9</volume><issue>1</issue><spage>10686</spage><epage>9</epage><pages>10686-9</pages><artnum>10686</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Activation of cell cycle regulated transcription during the G1-to-S transition initiates S phase entry and cell cycle commitment. The molecular mechanisms involving G1/S transcriptional regulation are well established and have been shown to be evolutionary conserved from yeast to humans. Previous work has suggested that changes to the chromatin state, specifically through histone acetylation, has an important role in the regulation of G1/S transcription in both yeast and human cells. Here we investigate the role of histone acetylation in G1/S transcriptional regulation in the budding yeast
Saccharomyces cerevisiae
. Our work shows that histone acetylation at specific sites at G1/S target gene promoters peaks at the G1-to-S transition, coinciding with their peak transcription levels. Acetylation at G1/S target promoters is significantly reduced upon deletion of the previously implicated histone acetyltransferase Gcn5, but G1/S cell cycle regulated transcription is largely unaffected. The histone deacetylase Rpd3, suggested to have a role in Whi5-dependent repression, is required for full repression of G1/S target genes in the G1 and S phases. However, in the context of transcriptionally active levels during the G1-to-S transition, this seems to play a minor role in the regulation of cell cycle transcription. Our data suggests that histone acetylation might modulate the amplitude of G1/S cell cycle regulated transcription in
Saccharomyces cerevisiae
, but has a limited role in its overall regulation.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31337860</pmid><doi>10.1038/s41598-019-47170-z</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8169-8735</orcidid><orcidid>https://orcid.org/0000-0002-2290-9675</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2045-2322 |
ispartof | Scientific reports, 2019-07, Vol.9 (1), p.10686-9, Article 10686 |
issn | 2045-2322 2045-2322 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6650506 |
source | PMC (PubMed Central); Full-Text Journals in Chemistry (Open access); Publicly Available Content (ProQuest); Springer Nature - nature.com Journals - Fully Open Access |
subjects | 38/22 38/77 631/337/572 631/80/641/2350 Acetylation Cell activation Cell cycle Cell Cycle - physiology Cell Cycle Proteins - genetics Cell Cycle Proteins - metabolism Chromatin Clonal deletion Evolutionary conservation Gene deletion Gene Expression Regulation, Fungal Gene regulation Histone acetyltransferase Histone Acetyltransferases - genetics Histone Acetyltransferases - metabolism Histone deacetylase Histone Deacetylases - genetics Histone Deacetylases - metabolism Humanities and Social Sciences Molecular modelling multidisciplinary Promoter Regions, Genetic Promoters S phase S Phase - physiology Saccharomyces cerevisiae Saccharomyces cerevisiae Proteins - genetics Saccharomyces cerevisiae Proteins - metabolism Science Science (multidisciplinary) Transcription Yeast Yeasts |
title | Gcn5 and Rpd3 have a limited role in the regulation of cell cycle transcripts during the G1 and S phases in Saccharomyces cerevisiae |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T00%3A15%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Gcn5%20and%20Rpd3%20have%20a%20limited%20role%20in%20the%20regulation%20of%20cell%20cycle%20transcripts%20during%20the%20G1%20and%20S%20phases%20in%20Saccharomyces%20cerevisiae&rft.jtitle=Scientific%20reports&rft.au=Kishkevich,%20A.&rft.date=2019-07-23&rft.volume=9&rft.issue=1&rft.spage=10686&rft.epage=9&rft.pages=10686-9&rft.artnum=10686&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/s41598-019-47170-z&rft_dat=%3Cproquest_pubme%3E2297179590%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c511t-b183571563db0360ff24615e2daed0218ac9b9349b33d4cbd42d9beb884028e53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2297179590&rft_id=info:pmid/31337860&rfr_iscdi=true |