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Identification of chilling-responsive transcripts in peanut ( Arachis hypogaea L.)
To isolate differentially expressed peanut genes responsive to chilling, a suppression subtractive hybridization (SSH) cDNA library was constructed for a chilling tolerant peanut cultivar A4 with mRNAs extracted from the seeds imbibed at 2°C and 15°C, respectively, for 24 hrs. A total of 466 cDNA cl...
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Published in: | Electronic Journal of Biotechnology 2012-10, Vol.14 (5) |
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container_title | Electronic Journal of Biotechnology |
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creator | Tang, Yue Yi Wang, Chuan Tang Yang, Guan Pin Feng, Tong Gao, Hua Yuan Wang, Xiu Zhen Chi, Xiao Yuan Xu, Ya Long Wu, Qi Chen, Dian Xu |
description | To isolate differentially expressed peanut genes responsive to
chilling, a suppression subtractive hybridization (SSH) cDNA library
was constructed for a chilling tolerant peanut cultivar A4 with mRNAs
extracted from the seeds imbibed at 2°C and 15°C,
respectively, for 24 hrs. A total of 466 cDNA clones were sequenced,
from which 193 unique transcripts (73 contigs and 120 singlets) were
assembled. Of these unique transcripts, 132 (68.4%) were significantly
similar to the sequences in GenBank non-redundant (nr) protein
database, which belonged to diverse functional categories including
metabolism, signal transduction, stress response, cell defense and
transcriptional regulation. The remaining 61 (31.6%) showed no
similarity to either hypothetical or known proteins. Six differentially
expressed transcripts were further confirmed with real-time
quantitative PCR (RT-qPCR). |
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chilling, a suppression subtractive hybridization (SSH) cDNA library
was constructed for a chilling tolerant peanut cultivar A4 with mRNAs
extracted from the seeds imbibed at 2°C and 15°C,
respectively, for 24 hrs. A total of 466 cDNA clones were sequenced,
from which 193 unique transcripts (73 contigs and 120 singlets) were
assembled. Of these unique transcripts, 132 (68.4%) were significantly
similar to the sequences in GenBank non-redundant (nr) protein
database, which belonged to diverse functional categories including
metabolism, signal transduction, stress response, cell defense and
transcriptional regulation. The remaining 61 (31.6%) showed no
similarity to either hypothetical or known proteins. Six differentially
expressed transcripts were further confirmed with real-time
quantitative PCR (RT-qPCR).</description><identifier>ISSN: 0717-3458</identifier><identifier>EISSN: 0717-3458</identifier><language>eng</language><publisher>Universidad Católica de Valparaíso</publisher><subject>chilling response, peanut, real-time quantitative PCR, suppression subtractive hybridization</subject><ispartof>Electronic Journal of Biotechnology, 2012-10, Vol.14 (5)</ispartof><rights>Copyright 2011 - Electronic Journal of Biotechnology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Tang, Yue Yi</creatorcontrib><creatorcontrib>Wang, Chuan Tang</creatorcontrib><creatorcontrib>Yang, Guan Pin</creatorcontrib><creatorcontrib>Feng, Tong</creatorcontrib><creatorcontrib>Gao, Hua Yuan</creatorcontrib><creatorcontrib>Wang, Xiu Zhen</creatorcontrib><creatorcontrib>Chi, Xiao Yuan</creatorcontrib><creatorcontrib>Xu, Ya Long</creatorcontrib><creatorcontrib>Wu, Qi</creatorcontrib><creatorcontrib>Chen, Dian Xu</creatorcontrib><title>Identification of chilling-responsive transcripts in peanut ( Arachis hypogaea L.)</title><title>Electronic Journal of Biotechnology</title><description>To isolate differentially expressed peanut genes responsive to
chilling, a suppression subtractive hybridization (SSH) cDNA library
was constructed for a chilling tolerant peanut cultivar A4 with mRNAs
extracted from the seeds imbibed at 2°C and 15°C,
respectively, for 24 hrs. A total of 466 cDNA clones were sequenced,
from which 193 unique transcripts (73 contigs and 120 singlets) were
assembled. Of these unique transcripts, 132 (68.4%) were significantly
similar to the sequences in GenBank non-redundant (nr) protein
database, which belonged to diverse functional categories including
metabolism, signal transduction, stress response, cell defense and
transcriptional regulation. The remaining 61 (31.6%) showed no
similarity to either hypothetical or known proteins. Six differentially
expressed transcripts were further confirmed with real-time
quantitative PCR (RT-qPCR).</description><subject>chilling response, peanut, real-time quantitative PCR, suppression subtractive hybridization</subject><issn>0717-3458</issn><issn>0717-3458</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqVjM0KwjAQhIMoWH_eYY96qKQ2pV5FFAVP4r2sNW231CQkUejbm4OCV2FghmHmG7CI50kepyLbDH_ymE2cazlfc5GLiF1Od6k8VVSiJ61AV1A21HWk6thKZ7Ry9JLgLSpXWjLeASkwEtXTwwK2FsPcQdMbXaNEOK-WMzaqsHNy_vEpWx32190xvpEOXFkYSw-0fRF4WHxL2QYlCc9E-vfhDYdmSyU</recordid><startdate>20121018</startdate><enddate>20121018</enddate><creator>Tang, Yue Yi</creator><creator>Wang, Chuan Tang</creator><creator>Yang, Guan Pin</creator><creator>Feng, Tong</creator><creator>Gao, Hua Yuan</creator><creator>Wang, Xiu Zhen</creator><creator>Chi, Xiao Yuan</creator><creator>Xu, Ya Long</creator><creator>Wu, Qi</creator><creator>Chen, Dian Xu</creator><general>Universidad Católica de Valparaíso</general><scope>RBI</scope></search><sort><creationdate>20121018</creationdate><title>Identification of chilling-responsive transcripts in peanut ( Arachis hypogaea L.)</title><author>Tang, Yue Yi ; Wang, Chuan Tang ; Yang, Guan Pin ; Feng, Tong ; Gao, Hua Yuan ; Wang, Xiu Zhen ; Chi, Xiao Yuan ; Xu, Ya Long ; Wu, Qi ; Chen, Dian Xu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-bioline_primary_cria_bioline_ej_ej110543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>chilling response, peanut, real-time quantitative PCR, suppression subtractive hybridization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tang, Yue Yi</creatorcontrib><creatorcontrib>Wang, Chuan Tang</creatorcontrib><creatorcontrib>Yang, Guan Pin</creatorcontrib><creatorcontrib>Feng, Tong</creatorcontrib><creatorcontrib>Gao, Hua Yuan</creatorcontrib><creatorcontrib>Wang, Xiu Zhen</creatorcontrib><creatorcontrib>Chi, Xiao Yuan</creatorcontrib><creatorcontrib>Xu, Ya Long</creatorcontrib><creatorcontrib>Wu, Qi</creatorcontrib><creatorcontrib>Chen, Dian Xu</creatorcontrib><collection>Bioline International</collection><jtitle>Electronic Journal of Biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tang, Yue Yi</au><au>Wang, Chuan Tang</au><au>Yang, Guan Pin</au><au>Feng, Tong</au><au>Gao, Hua Yuan</au><au>Wang, Xiu Zhen</au><au>Chi, Xiao Yuan</au><au>Xu, Ya Long</au><au>Wu, Qi</au><au>Chen, Dian Xu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of chilling-responsive transcripts in peanut ( Arachis hypogaea L.)</atitle><jtitle>Electronic Journal of Biotechnology</jtitle><date>2012-10-18</date><risdate>2012</risdate><volume>14</volume><issue>5</issue><issn>0717-3458</issn><eissn>0717-3458</eissn><abstract>To isolate differentially expressed peanut genes responsive to
chilling, a suppression subtractive hybridization (SSH) cDNA library
was constructed for a chilling tolerant peanut cultivar A4 with mRNAs
extracted from the seeds imbibed at 2°C and 15°C,
respectively, for 24 hrs. A total of 466 cDNA clones were sequenced,
from which 193 unique transcripts (73 contigs and 120 singlets) were
assembled. Of these unique transcripts, 132 (68.4%) were significantly
similar to the sequences in GenBank non-redundant (nr) protein
database, which belonged to diverse functional categories including
metabolism, signal transduction, stress response, cell defense and
transcriptional regulation. The remaining 61 (31.6%) showed no
similarity to either hypothetical or known proteins. Six differentially
expressed transcripts were further confirmed with real-time
quantitative PCR (RT-qPCR).</abstract><pub>Universidad Católica de Valparaíso</pub></addata></record> |
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subjects | chilling response, peanut, real-time quantitative PCR, suppression subtractive hybridization |
title | Identification of chilling-responsive transcripts in peanut ( Arachis hypogaea L.) |
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