| Literature DB >> 31885871 |
Shuai Zhang1,2, Qingcui Zhao1,2, Daxing Zeng1,2, Jiehua Xu1,2, Hougao Zhou3, Fenglan Wang3, Nan Ma4, Yonghong Li1,2.
Abstract
[This corrects the article DOI: 10.1038/s41438-019-0221-8.].Entities:
Keywords: Plant hormones; Plant signalling
Year: 2019 PMID: 31885871 PMCID: PMC6932989 DOI: 10.1038/s41438-019-0230-7
Source DB: PubMed Journal: Hortic Res ISSN: 2052-7276 Impact factor: 6.793
Fig. 7a qRT-PCR analysis of SAG expression in RhMYB108-silenced petals. b Interaction of RhMYB108 protein with the SAG promoter regions, as revealed using yeast one-hybrid assays. Interactions were determined based on yeast cell growth and were confirmed by the color indication of X-β-gal on SD/-Trp/-Ura medium plates. c, d Images of firefly luciferase fluorescence signals and relative reporter activity (LUC/REN) in N. benthamiana leaves. RhMYB108 protein was separately coexpressed with pNAC053::LUC, pNAC092::LUC and pSAG113::LUC in tobacco leaves. After 48 h of Agrobacterium tumefaciens infiltration, live LUC images and relative LUC activity (LUC/REN) in tobacco leaves were assayed. The error bars represent the means of six biological replicates, and the asterisks indicate statistically significant differences according to Student’s t test (*P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001).