2012
DOI: 10.1093/jxb/ers042
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Involvement of PpDof1 transcriptional repressor in the nutrient condition-dependent growth control of protonemal filaments in Physcomitrella patens

Abstract: In higher plants, the Dof transcription factors that harbour a conserved plant-specific DNA-binding domain function in the regulation of diverse biological processes that are unique to plants. Although these factors are present in both higher and lower plants, they have not yet been characterized in lower plants. Here six genes encoding Dof transcription factors in the moss Physcomitrella patens are characterized and two of these genes, PpDof1 and PpDof2, are functionally analysed. The targeted disruption of P… Show more

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Cited by 33 publications
(24 citation statements)
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References 58 publications
(73 reference statements)
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“…Then, the regions encoding the Dof domains of PpDof3 and PpDof4 in the resultant plasmids were replaced with a 35S promoterdriven hygromycin resistance gene or a 35S promoterdriven kanamycin resistance gene (Sugiyama et al 2012). Transformation of P. patens with these targeting vectors was performed by the polyethylene glycol method, and the transformants were selected on agar plates containing appropriate concentrations of antibiotics according to the method described previously (Sugiyama et al 2012). Genomic Southern blot analysis was performed with EcoRV-digested genomic DNA from the protonema of the wild type and disruptant lines, as described previously (Sugiyama et al 2012).…”
Section: Generation Of P Patens Disruptants and Genomic Southern Blomentioning
confidence: 99%
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“…Then, the regions encoding the Dof domains of PpDof3 and PpDof4 in the resultant plasmids were replaced with a 35S promoterdriven hygromycin resistance gene or a 35S promoterdriven kanamycin resistance gene (Sugiyama et al 2012). Transformation of P. patens with these targeting vectors was performed by the polyethylene glycol method, and the transformants were selected on agar plates containing appropriate concentrations of antibiotics according to the method described previously (Sugiyama et al 2012). Genomic Southern blot analysis was performed with EcoRV-digested genomic DNA from the protonema of the wild type and disruptant lines, as described previously (Sugiyama et al 2012).…”
Section: Generation Of P Patens Disruptants and Genomic Southern Blomentioning
confidence: 99%
“…Transformation of P. patens with these targeting vectors was performed by the polyethylene glycol method, and the transformants were selected on agar plates containing appropriate concentrations of antibiotics according to the method described previously (Sugiyama et al 2012). Genomic Southern blot analysis was performed with EcoRV-digested genomic DNA from the protonema of the wild type and disruptant lines, as described previously (Sugiyama et al 2012). PpDof3-and PpDof4-specific DNA probes were prepared by PCR using the gene-specific primers listed in Supplemental Table S1.…”
Section: Generation Of P Patens Disruptants and Genomic Southern Blomentioning
confidence: 99%
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