2014
DOI: 10.1093/jxb/eru202
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HDG11 upregulates cell-wall-loosening protein genes to promote root elongation in Arabidopsis

Abstract: SummaryEDT1/HGD11 coordinately upregulates gene families of cell-wall-loosening proteins to alter cell-wall extensibility and promote primary root elongation.

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Cited by 83 publications
(67 citation statements)
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“…A similar induction pattern of several expansin genes was also observed in Arabidopsis under soil water-deficit treatment (Harb et al, 2010). Consistent with these findings, overexpression of expansin genes has been reported to confer tolerance to various water-deficit stresses in different plant species, likely by maintaining root elongation, though these results should not be overinterpreted, as overexpression of expansins may lead to many pleiotropic effects on physiology that are not directly related to root growth (Guo et al, 2011;Lü et al, 2013;Xu et al, 2014).…”
Section: Changes In the Cell Wall Enable Growth Recoverysupporting
confidence: 69%
“…A similar induction pattern of several expansin genes was also observed in Arabidopsis under soil water-deficit treatment (Harb et al, 2010). Consistent with these findings, overexpression of expansin genes has been reported to confer tolerance to various water-deficit stresses in different plant species, likely by maintaining root elongation, though these results should not be overinterpreted, as overexpression of expansins may lead to many pleiotropic effects on physiology that are not directly related to root growth (Guo et al, 2011;Lü et al, 2013;Xu et al, 2014).…”
Section: Changes In the Cell Wall Enable Growth Recoverysupporting
confidence: 69%
“…The 35S‐HA‐ EDT1 / HDG11 transgenic plants were generated and the plants showing similar phenotype to edt1D mutant were used for ChIP assay (Xu et al ). The promoter fragments enriched by anti‐HA antibodies (Abmart, http://www.ab-mart.com.cn) can be detected by PCR.…”
Section: Resultsmentioning
confidence: 99%
“…We provide multiple lines of supporting evidence including yeast-one-hybrid, EMSA and ChIP assays, as well as the genetic analysis that established the interaction between ERF109 and the promoters of both ASA1 and YUC2 genes (Figs 6 and 7). The native promoter of ERF109 was initially used for ChIP assay without success, which was probably due to low expression level of ERF109, and has been similarly noted for other transcription factors with low expression 51 . However, when we used a stronger promoter, the results showed that ASA1 and YUC2 were targets of ERF109.…”
Section: Discussionmentioning
confidence: 99%