Serum availability affects expression of common house-keeping genes in colon adenocarcinoma cell lines: implications for quantitative real-time PCR studies
Careful selection of housekeeping genes (HKG) is prerequisite to yield sound qPCR results. HKG expression varies in response to hypoxia but the effect of manipulations of serum availability, a common experimental procedure, remains unknown. Also, no data on HKG expression stability across colon aden...
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creator | Krzystek-Korpacka, Malgorzata Hotowy, Katarzyna Czapinska, Elzbieta Podkowik, Magdalena Bania, Jacek Gamian, Andrzej Bednarz-Misa, Iwona |
description | Careful selection of housekeeping genes (HKG) is prerequisite to yield sound qPCR results. HKG expression varies in response to hypoxia but the effect of manipulations of serum availability, a common experimental procedure, remains unknown. Also, no data on HKG expression stability across colon adenocarcinoma lines that would aid selection of normalizers suitable for studies involving several lines are available. Thus, we evaluated the effect of serum availability on the expression of commonly used HKG (
ACTB
,
B2M
,
GAPDH
,
GUSB
,
HPRT1
,
IPO8
,
MRPL19
,
PGK1
,
PPIA
,
RPLP0
,
RPS23
,
SDHA
,
TBP
,
UBC
, and
YWHAZ
) in seven colon adenocarcinoma cell lines (Caco-2, DLD-1, HCT116, HT29, Lovo, SW480, and SW620). Sets of stably expressed line-specific and pan-line HKG were validated against absolutely quantified
CDKN1A
,
TP53
, and
MDK
transcripts. Both serum availability and line type affected HKG expression.
UBC
was fourfold down-regulated and
HPRT1
1.75-fold up-regulated in re-fed HT29 cultures. Line-to-line variability in HKG expression was more pronounced than that caused by altering serum availability and could be found even between isogenic cell lines.
PPIA
,
RPLP0
,
YWHAZ
, and
IPO8
were repeatedly highly ranked while
ACTB
,
B2M
,
UBC
, and
PGK1
were ranked poorly. Normalization against
PPIA
/
RPLP0
/
SDHA
was found optimal for studies involving various colon adenocarcinoma cell lines subjected to manipulations of serum availability. We found HKG expression to vary, more pronouncedly by line type than growth conditions with significant differences also between isogenic cell lines. Although using line-specific normalizers remains optimal, a set of pan-line HKG that yields good estimation of relative expression of target genes was proposed. |
doi_str_mv | 10.1007/s10616-016-9971-4 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5101321</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2918264884</sourcerecordid><originalsourceid>FETCH-LOGICAL-c535t-c8bc66ae0f10846e74528bc98547f7b564540de06605e6d027ab10b559355dfa3</originalsourceid><addsrcrecordid>eNp9ksuKFDEUhoMoTjv6AG4k4MZN6UmlcikXgjTeYEDxsg6p1KmejFVJT1LVOM_iy5qix2EUdBESzv-dPznhJ-Qxg-cMQL3IDCSTFZTVtopVzR2yYULxCpTSd8kG2hqqFmR7Qh7kfAEAheL3yUmtOG8bqTfk5xdMy0TtwfrRdn708xW1w4BuzhR_7BPm7GOgcaAuTlM5ncclY_Udce_Dju4wYKY-FHUsou0xRGeT8yFOljocRzr6grykftqP3tm5uGU6xEQvFxtmP5fKAWlCO1azn5B-2n6meV56j_khuTfYMeOj6_2UfHv75uv2fXX28d2H7euzygku5srpzklpEQYGupGoGlGXUqtFowbVCdmIBnoEKUGg7KFWtmPQCdFyIfrB8lPy6ui7X7oJe4dhTnY0--Qnm65MtN78qQR_bnbxYAQDxmtWDJ5dG6R4uWCezeTzOrwNWL7LMF1LBUJpVdCnf6EXcUmhjGfqduUarZv_UUzrMiUXfKXYkXIp5pxwuHkyA7MGxBwDYkpAzBoQs_Y8uT3rTcfvRBSgPgK5SGGH6dbV_3T9BaMSyRg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2918264884</pqid></control><display><type>article</type><title>Serum availability affects expression of common house-keeping genes in colon adenocarcinoma cell lines: implications for quantitative real-time PCR studies</title><source>PubMed (Medline)</source><source>Springer journals</source><source>ProQuest Central UK/Ireland</source><source>EZB Electronic Journals Library</source><source>ProQuest Central</source><creator>Krzystek-Korpacka, Malgorzata ; Hotowy, Katarzyna ; Czapinska, Elzbieta ; Podkowik, Magdalena ; Bania, Jacek ; Gamian, Andrzej ; Bednarz-Misa, Iwona</creator><creatorcontrib>Krzystek-Korpacka, Malgorzata ; Hotowy, Katarzyna ; Czapinska, Elzbieta ; Podkowik, Magdalena ; Bania, Jacek ; Gamian, Andrzej ; Bednarz-Misa, Iwona</creatorcontrib><description>Careful selection of housekeeping genes (HKG) is prerequisite to yield sound qPCR results. HKG expression varies in response to hypoxia but the effect of manipulations of serum availability, a common experimental procedure, remains unknown. Also, no data on HKG expression stability across colon adenocarcinoma lines that would aid selection of normalizers suitable for studies involving several lines are available. Thus, we evaluated the effect of serum availability on the expression of commonly used HKG (
ACTB
,
B2M
,
GAPDH
,
GUSB
,
HPRT1
,
IPO8
,
MRPL19
,
PGK1
,
PPIA
,
RPLP0
,
RPS23
,
SDHA
,
TBP
,
UBC
, and
YWHAZ
) in seven colon adenocarcinoma cell lines (Caco-2, DLD-1, HCT116, HT29, Lovo, SW480, and SW620). Sets of stably expressed line-specific and pan-line HKG were validated against absolutely quantified
CDKN1A
,
TP53
, and
MDK
transcripts. Both serum availability and line type affected HKG expression.
UBC
was fourfold down-regulated and
HPRT1
1.75-fold up-regulated in re-fed HT29 cultures. Line-to-line variability in HKG expression was more pronounced than that caused by altering serum availability and could be found even between isogenic cell lines.
PPIA
,
RPLP0
,
YWHAZ
, and
IPO8
were repeatedly highly ranked while
ACTB
,
B2M
,
UBC
, and
PGK1
were ranked poorly. Normalization against
PPIA
/
RPLP0
/
SDHA
was found optimal for studies involving various colon adenocarcinoma cell lines subjected to manipulations of serum availability. We found HKG expression to vary, more pronouncedly by line type than growth conditions with significant differences also between isogenic cell lines. Although using line-specific normalizers remains optimal, a set of pan-line HKG that yields good estimation of relative expression of target genes was proposed.</description><identifier>ISSN: 0920-9069</identifier><identifier>EISSN: 1573-0778</identifier><identifier>DOI: 10.1007/s10616-016-9971-4</identifier><identifier>PMID: 27339468</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Adenocarcinoma ; Automation ; Biochemistry ; Biomedicine ; Biotechnology ; Cancer ; Cell culture ; Chemistry ; Chemistry and Materials Science ; Colon ; Dehydrogenases ; Enzymes ; Genes ; Glyceraldehyde-3-phosphate dehydrogenase ; Growth conditions ; Hypoxia ; Kinases ; Original ; Original Article ; p53 Protein ; Polymerase chain reaction ; Proteins ; Signal transduction ; Tumor cell lines</subject><ispartof>Cytotechnology (Dordrecht), 2016-12, Vol.68 (6), p.2503-2517</ispartof><rights>The Author(s) 2016</rights><rights>Copyright Springer Science & Business Media 2016</rights><rights>The Author(s) 2016. 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-c535t-c8bc66ae0f10846e74528bc98547f7b564540de06605e6d027ab10b559355dfa3</citedby><cites>FETCH-LOGICAL-c535t-c8bc66ae0f10846e74528bc98547f7b564540de06605e6d027ab10b559355dfa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101321/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2918264884?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,21387,27923,27924,33743,33744,41487,42556,43804,51318,53790,53792,64384,64386,64388,72240</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27339468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krzystek-Korpacka, Malgorzata</creatorcontrib><creatorcontrib>Hotowy, Katarzyna</creatorcontrib><creatorcontrib>Czapinska, Elzbieta</creatorcontrib><creatorcontrib>Podkowik, Magdalena</creatorcontrib><creatorcontrib>Bania, Jacek</creatorcontrib><creatorcontrib>Gamian, Andrzej</creatorcontrib><creatorcontrib>Bednarz-Misa, Iwona</creatorcontrib><title>Serum availability affects expression of common house-keeping genes in colon adenocarcinoma cell lines: implications for quantitative real-time PCR studies</title><title>Cytotechnology (Dordrecht)</title><addtitle>Cytotechnology</addtitle><addtitle>Cytotechnology</addtitle><description>Careful selection of housekeeping genes (HKG) is prerequisite to yield sound qPCR results. HKG expression varies in response to hypoxia but the effect of manipulations of serum availability, a common experimental procedure, remains unknown. Also, no data on HKG expression stability across colon adenocarcinoma lines that would aid selection of normalizers suitable for studies involving several lines are available. Thus, we evaluated the effect of serum availability on the expression of commonly used HKG (
ACTB
,
B2M
,
GAPDH
,
GUSB
,
HPRT1
,
IPO8
,
MRPL19
,
PGK1
,
PPIA
,
RPLP0
,
RPS23
,
SDHA
,
TBP
,
UBC
, and
YWHAZ
) in seven colon adenocarcinoma cell lines (Caco-2, DLD-1, HCT116, HT29, Lovo, SW480, and SW620). Sets of stably expressed line-specific and pan-line HKG were validated against absolutely quantified
CDKN1A
,
TP53
, and
MDK
transcripts. Both serum availability and line type affected HKG expression.
UBC
was fourfold down-regulated and
HPRT1
1.75-fold up-regulated in re-fed HT29 cultures. Line-to-line variability in HKG expression was more pronounced than that caused by altering serum availability and could be found even between isogenic cell lines.
PPIA
,
RPLP0
,
YWHAZ
, and
IPO8
were repeatedly highly ranked while
ACTB
,
B2M
,
UBC
, and
PGK1
were ranked poorly. Normalization against
PPIA
/
RPLP0
/
SDHA
was found optimal for studies involving various colon adenocarcinoma cell lines subjected to manipulations of serum availability. We found HKG expression to vary, more pronouncedly by line type than growth conditions with significant differences also between isogenic cell lines. Although using line-specific normalizers remains optimal, a set of pan-line HKG that yields good estimation of relative expression of target genes was proposed.</description><subject>Adenocarcinoma</subject><subject>Automation</subject><subject>Biochemistry</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Cancer</subject><subject>Cell culture</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Colon</subject><subject>Dehydrogenases</subject><subject>Enzymes</subject><subject>Genes</subject><subject>Glyceraldehyde-3-phosphate dehydrogenase</subject><subject>Growth conditions</subject><subject>Hypoxia</subject><subject>Kinases</subject><subject>Original</subject><subject>Original Article</subject><subject>p53 Protein</subject><subject>Polymerase chain reaction</subject><subject>Proteins</subject><subject>Signal transduction</subject><subject>Tumor cell lines</subject><issn>0920-9069</issn><issn>1573-0778</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9ksuKFDEUhoMoTjv6AG4k4MZN6UmlcikXgjTeYEDxsg6p1KmejFVJT1LVOM_iy5qix2EUdBESzv-dPznhJ-Qxg-cMQL3IDCSTFZTVtopVzR2yYULxCpTSd8kG2hqqFmR7Qh7kfAEAheL3yUmtOG8bqTfk5xdMy0TtwfrRdn708xW1w4BuzhR_7BPm7GOgcaAuTlM5ncclY_Udce_Dju4wYKY-FHUsou0xRGeT8yFOljocRzr6grykftqP3tm5uGU6xEQvFxtmP5fKAWlCO1azn5B-2n6meV56j_khuTfYMeOj6_2UfHv75uv2fXX28d2H7euzygku5srpzklpEQYGupGoGlGXUqtFowbVCdmIBnoEKUGg7KFWtmPQCdFyIfrB8lPy6ui7X7oJe4dhTnY0--Qnm65MtN78qQR_bnbxYAQDxmtWDJ5dG6R4uWCezeTzOrwNWL7LMF1LBUJpVdCnf6EXcUmhjGfqduUarZv_UUzrMiUXfKXYkXIp5pxwuHkyA7MGxBwDYkpAzBoQs_Y8uT3rTcfvRBSgPgK5SGGH6dbV_3T9BaMSyRg</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Krzystek-Korpacka, Malgorzata</creator><creator>Hotowy, Katarzyna</creator><creator>Czapinska, Elzbieta</creator><creator>Podkowik, Magdalena</creator><creator>Bania, Jacek</creator><creator>Gamian, Andrzej</creator><creator>Bednarz-Misa, Iwona</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20161201</creationdate><title>Serum availability affects expression of common house-keeping genes in colon adenocarcinoma cell lines: implications for quantitative real-time PCR studies</title><author>Krzystek-Korpacka, Malgorzata ; Hotowy, Katarzyna ; Czapinska, Elzbieta ; Podkowik, Magdalena ; Bania, Jacek ; Gamian, Andrzej ; Bednarz-Misa, Iwona</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c535t-c8bc66ae0f10846e74528bc98547f7b564540de06605e6d027ab10b559355dfa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adenocarcinoma</topic><topic>Automation</topic><topic>Biochemistry</topic><topic>Biomedicine</topic><topic>Biotechnology</topic><topic>Cancer</topic><topic>Cell culture</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Colon</topic><topic>Dehydrogenases</topic><topic>Enzymes</topic><topic>Genes</topic><topic>Glyceraldehyde-3-phosphate dehydrogenase</topic><topic>Growth conditions</topic><topic>Hypoxia</topic><topic>Kinases</topic><topic>Original</topic><topic>Original Article</topic><topic>p53 Protein</topic><topic>Polymerase chain reaction</topic><topic>Proteins</topic><topic>Signal transduction</topic><topic>Tumor cell lines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krzystek-Korpacka, Malgorzata</creatorcontrib><creatorcontrib>Hotowy, Katarzyna</creatorcontrib><creatorcontrib>Czapinska, Elzbieta</creatorcontrib><creatorcontrib>Podkowik, Magdalena</creatorcontrib><creatorcontrib>Bania, Jacek</creatorcontrib><creatorcontrib>Gamian, Andrzej</creatorcontrib><creatorcontrib>Bednarz-Misa, Iwona</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central UK/Ireland</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</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cytotechnology (Dordrecht)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krzystek-Korpacka, Malgorzata</au><au>Hotowy, Katarzyna</au><au>Czapinska, Elzbieta</au><au>Podkowik, Magdalena</au><au>Bania, Jacek</au><au>Gamian, Andrzej</au><au>Bednarz-Misa, Iwona</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum availability affects expression of common house-keeping genes in colon adenocarcinoma cell lines: implications for quantitative real-time PCR studies</atitle><jtitle>Cytotechnology (Dordrecht)</jtitle><stitle>Cytotechnology</stitle><addtitle>Cytotechnology</addtitle><date>2016-12-01</date><risdate>2016</risdate><volume>68</volume><issue>6</issue><spage>2503</spage><epage>2517</epage><pages>2503-2517</pages><issn>0920-9069</issn><eissn>1573-0778</eissn><abstract>Careful selection of housekeeping genes (HKG) is prerequisite to yield sound qPCR results. HKG expression varies in response to hypoxia but the effect of manipulations of serum availability, a common experimental procedure, remains unknown. Also, no data on HKG expression stability across colon adenocarcinoma lines that would aid selection of normalizers suitable for studies involving several lines are available. Thus, we evaluated the effect of serum availability on the expression of commonly used HKG (
ACTB
,
B2M
,
GAPDH
,
GUSB
,
HPRT1
,
IPO8
,
MRPL19
,
PGK1
,
PPIA
,
RPLP0
,
RPS23
,
SDHA
,
TBP
,
UBC
, and
YWHAZ
) in seven colon adenocarcinoma cell lines (Caco-2, DLD-1, HCT116, HT29, Lovo, SW480, and SW620). Sets of stably expressed line-specific and pan-line HKG were validated against absolutely quantified
CDKN1A
,
TP53
, and
MDK
transcripts. Both serum availability and line type affected HKG expression.
UBC
was fourfold down-regulated and
HPRT1
1.75-fold up-regulated in re-fed HT29 cultures. Line-to-line variability in HKG expression was more pronounced than that caused by altering serum availability and could be found even between isogenic cell lines.
PPIA
,
RPLP0
,
YWHAZ
, and
IPO8
were repeatedly highly ranked while
ACTB
,
B2M
,
UBC
, and
PGK1
were ranked poorly. Normalization against
PPIA
/
RPLP0
/
SDHA
was found optimal for studies involving various colon adenocarcinoma cell lines subjected to manipulations of serum availability. We found HKG expression to vary, more pronouncedly by line type than growth conditions with significant differences also between isogenic cell lines. Although using line-specific normalizers remains optimal, a set of pan-line HKG that yields good estimation of relative expression of target genes was proposed.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>27339468</pmid><doi>10.1007/s10616-016-9971-4</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Automation Biochemistry Biomedicine Biotechnology Cancer Cell culture Chemistry Chemistry and Materials Science Colon Dehydrogenases Enzymes Genes Glyceraldehyde-3-phosphate dehydrogenase Growth conditions Hypoxia Kinases Original Original Article p53 Protein Polymerase chain reaction Proteins Signal transduction Tumor cell lines |
title | Serum availability affects expression of common house-keeping genes in colon adenocarcinoma cell lines: implications for quantitative real-time PCR studies |
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