2018
DOI: 10.1007/s11105-018-1075-1
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Expression Profiling of the CSDP Transcription Factor Gene Family Points to Roles in Organ Development and Abiotic Stress Response in Tomato (Solanum lycopersicum L.)

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Cited by 4 publications
(3 citation statements)
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“…Leaves were collected at various time points: 0, 1, 3, 6, 12, and 24 h after onset of treatment. Tomato plants were incubated in a growth cabinet at 40 °C (heat treatment) or 4 °C (cold treatment) for 24 h. NaCl stress treatment was imposed by submerging plant roots in a 200 mM NaCl solution for 24 h. For NWD stress, whole plants were gently pulled out from the soil, their root systems carefully cleaned with fresh water and subsequently placed on a dry paper towel for 24 h [ 54 , 55 , 56 , 57 , 58 ]. ABA treatment was applied by spraying plant leaves with 100 μM ABA [ 54 ].…”
Section: Methodsmentioning
confidence: 99%
“…Leaves were collected at various time points: 0, 1, 3, 6, 12, and 24 h after onset of treatment. Tomato plants were incubated in a growth cabinet at 40 °C (heat treatment) or 4 °C (cold treatment) for 24 h. NaCl stress treatment was imposed by submerging plant roots in a 200 mM NaCl solution for 24 h. For NWD stress, whole plants were gently pulled out from the soil, their root systems carefully cleaned with fresh water and subsequently placed on a dry paper towel for 24 h [ 54 , 55 , 56 , 57 , 58 ]. ABA treatment was applied by spraying plant leaves with 100 μM ABA [ 54 ].…”
Section: Methodsmentioning
confidence: 99%
“…Seedling was harvested first and that represented both shoots and roots. That's why seedlings were taken as a calibrator Whereas the leaf samples were collected at 0 h after treatment was the calibrator for abiotic stress and hormone treatments [49]. Primers used for qRT-PCR based gene expression analysis were designed using Primer3 software (http://frodo.wi.mit.edu/primer3/ input.htm) software (Table S1).…”
Section: Rna Preparation Cdna Synthesis Rt-pcr and Qrt-pcr Analysesmentioning
confidence: 99%
“…LOC101268350) [45] and the relative amount of the ampli ed product was calculated following the 2 −ΔΔCt method [46]. Stem samples were used as calibrator for the expression analysis of organ samples whereas the leaf samples were collected at 0 h after treatment was the calibrator for abiotic stress and hormone treatments [47]. Primers used for qRT-PCR based gene expression analysis were designed using xx software (Table S1).…”
Section: Rna Preparation Cdna Synthesis Rt-pcr and Qrt-pcr Analysesmentioning
confidence: 99%