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      QsMYB1 expression is modulated in response to heat and drought stresses and during plant recovery in Quercus suber.

      1 , , , ,
      Plant physiology and biochemistry : PPB
      Elsevier BV
      5′-untranslated region, 5′UTR, Abiotic stress, Cork oak, DW, F, F(0), F(m), F(v), F(v)/F(m), FC, FW, Gene expression, MDA, R2R3-MYB, RT-qPCR, RWC, Recovery, TFs, TW, WS, WW, dry weight, field capacity, gDNA, genomic DNA, malondialdehyde, maximum fluorescence, maximum quantum yield of PSII photochemistry, minimum fluorescence, quantum yield of PSII photochemistry, relative water content, reverse transcription quantitative PCR, steady state fluorescence, tissue fresh weight, transcription factors, turgid weight, variable fluorescence, water stress, well watered, Ф(PSII)

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          Abstract

          Cork oak is an economically important forest species showing a great tolerance to high temperatures and shortage of water. However, the mechanisms underlying this plasticity are still poorly understood. Among the stress regulators, transcription factors (TFs) are especially important since they can control a wide range of stress-inducible genes, which make them powerful targets for genetic engineering of stress tolerance. Here we evaluated the influence of increasing temperatures (up to 55 °C) or drought (18% field capacity, FC) on the expression profile of an R2R3-MYB transcription factor of cork oak, the QsMYB1. QsMYB1 was previously identified as being preferentially expressed in cork tissues and as having an associated alternative splicing mechanism, which results in two different transcripts (QsMYB1.1 and QsMYB1.2). Expression analysis by reverse transcription quantitative PCR (RT-qPCR) revealed that increasing temperatures led to a gradual down-regulation of QsMYB1 transcripts with more effect on QsMYB1.1 abundance. On the other hand, under drought condition, expression of QsMYB1 variants, mainly the QsMYB1.2, was transiently up-regulated shortly after the stress imposition. Recovery from each stress has also resulted in a differential response by both QsMYB1 transcripts. Several physiological and biochemical parameters (plant water status, chlorophyll fluorescence, lipid peroxidation and proline content) were determined in order to monitor the plant performance under stress and recovery. In conclusion, this report provides the first evidence that QsMYB1 TF may have a putative function in the regulatory network of cork oak response to heat and drought stresses and during plant recovery.

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          Author and article information

          Journal
          Plant Physiol. Biochem.
          Plant physiology and biochemistry : PPB
          Elsevier BV
          1873-2690
          0981-9428
          Dec 2013
          : 73
          Affiliations
          [1 ] Centro de Biotecnologia Agrícola e Agro-Alimentar do Alentejo (CEBAL)/Instituto Politécnico de Beja (IPBeja), Rua Pedro Soares, 7801-908 Beja, Portugal; Centre for Research in Ceramics & Composite Materials (CICECO), University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal; Departament of Biology & Centre for Environmental and Marine Studies (CESAM), University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal. Electronic address: tania.almeida@cebal.pt.
          Article
          S0981-9428(13)00353-7
          10.1016/j.plaphy.2013.10.007
          24161757
          9f5f9d3b-1aad-4f0d-a496-006934ef4d48
          History

          5′-untranslated region,Ф(PSII),well watered,water stress,variable fluorescence,turgid weight,transcription factors,tissue fresh weight,steady state fluorescence,reverse transcription quantitative PCR,relative water content,quantum yield of PSII photochemistry,minimum fluorescence,maximum quantum yield of PSII photochemistry,maximum fluorescence,malondialdehyde,genomic DNA,gDNA,field capacity,dry weight,WW,WS,TW,TFs,Recovery,RWC,RT-qPCR,R2R3-MYB,MDA,Gene expression,FW,F(v)/F(m),F(v),F(m),F(0),F,DW,Cork oak,Abiotic stress,5′UTR,FC

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