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Identification of chilling-responsive transcripts in peanut (Arachis hypogaea L. )
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.
Afiliação
  • Tang, Yue Yi; Ocean University of China. College of Marine Life Sciences. Qingdao. CN
  • Wang, Chuan Tang; Shandong Peanut Research Institute. Qingdao. CN
  • Yang, Guan Pin; Ocean University of China. College of Marine Life Sciences. Qingdao. CN
  • Feng, Tong; Jilin Academy of Agricultural Sciences. Institute of Economic Plants. Gongzhuling. CN
  • Gao, Hua Yuan; Jilin Academy of Agricultural Sciences. Institute of Economic Plants. Gongzhuling. CN
  • Wang, Xiu Zhen; Shandong Peanut Research Institute. Qingdao. CN
  • Chi, Xiao Yuan; Shandong Peanut Research Institute. Qingdao. CN
  • Xu, Ya Long; Zhengzhou Tobacco Research Institute of CNTC. China Tobacco Gene Research Center. Zhengzhou. CN
  • Wu, Qi; Shandong Peanut Research Institute. Qingdao. CN
  • Chen, Dian Xu; Shandong Peanut Research Institute. Qingdao. CN
Electron. j. biotechnol ; 14(5): 5-5, Sept. 2011. ilus, tab
Artigo em Inglês | LILACS | ID: lil-640512
Biblioteca responsável: CL1.1
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 2ºC and 15ºC, 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 percent) 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 percent) showed no similarity to either hypothetical or known proteins. Six differentially expressed transcripts were further confirmed with real-time quantitative PCR (RT-qPCR).
Assuntos


Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Assunto principal: Arachis / Reação em Cadeia da Polimerase / Temperatura Baixa / Hibridização de Ácido Nucleico Tipo de estudo: Estudo diagnóstico Idioma: Inglês Revista: Electron. j. biotechnol Assunto da revista: Biotecnologia Ano de publicação: 2011 Tipo de documento: Artigo / Documento de projeto País de afiliação: China Instituição/País de afiliação: Jilin Academy of Agricultural Sciences/CN / Ocean University of China/CN / Shandong Peanut Research Institute/CN / Zhengzhou Tobacco Research Institute of CNTC/CN

Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Assunto principal: Arachis / Reação em Cadeia da Polimerase / Temperatura Baixa / Hibridização de Ácido Nucleico Tipo de estudo: Estudo diagnóstico Idioma: Inglês Revista: Electron. j. biotechnol Assunto da revista: Biotecnologia Ano de publicação: 2011 Tipo de documento: Artigo / Documento de projeto País de afiliação: China Instituição/País de afiliação: Jilin Academy of Agricultural Sciences/CN / Ocean University of China/CN / Shandong Peanut Research Institute/CN / Zhengzhou Tobacco Research Institute of CNTC/CN
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