dc.creator | Fonseca, J P | |
dc.creator | Menossi, M | |
dc.creator | Thibaud-Nissen, F | |
dc.creator | Town, C D | |
dc.date | 2010 | |
dc.date | 2015-11-27T13:17:36Z | |
dc.date | 2015-11-27T13:17:36Z | |
dc.date.accessioned | 2018-03-29T01:10:27Z | |
dc.date.available | 2018-03-29T01:10:27Z | |
dc.identifier | Genetics And Molecular Research : Gmr. v. 9, n. 1, p. 167-75, 2010. | |
dc.identifier | 1676-5680 | |
dc.identifier | 10.4238/vol9-1gmr704 | |
dc.identifier | http://www.ncbi.nlm.nih.gov/pubmed/20198573 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/198738 | |
dc.identifier | 20198573 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1298971 | |
dc.description | TGA factors play a key role in plant defense by binding to the promoter region of defense genes, inducing expression. Salicylic acid (SA) induces the expression of the gene encoding NIMIN-1, which interacts with NPR1/NIM1, a key regulator of systemic acquired resistance. We investigated whether the TGA2-binding motif TGACG located upstream of the NIMIN-1 gene is necessary for SA induction of NIMIN-1 expression. A mutated version of the NIMIN-1 promoter was created by site-directed mutagenesis. We generated T-DNA constructs in which native NIMIN-1 and mutated promoters were fused to green fluorescent protein and beta-glucuronidase reporters. We produced transgenic Arabidopsis plants and observed NIMIN-1 promoter-driven green fluorescent protein expression in the roots, petiole and leaves. Constructs were agroinfiltrated into the leaves for transient quantitative assays of gene expression. Using quantitative real-time RT-PCR, we characterized the normal gene response to SA and compared it to the response of the mutant version of the NIMIN-1 promoter. Both the native NIMIN-1 construct and an endogenous copy of NIMIN-1 were induced by SA. However, the mutated promoter construct was much less sensitive to SA than the native NIMIN-1 promoter, indicating that this TGA2-binding motif is directly involved in the modulation of SA-induced NIMIN-1 expression in Arabidopsis. | |
dc.description | 9 | |
dc.description | 167-75 | |
dc.language | eng | |
dc.relation | Genetics And Molecular Research : Gmr | |
dc.relation | Genet. Mol. Res. | |
dc.rights | aberto | |
dc.rights | | |
dc.source | PubMed | |
dc.subject | Arabidopsis | |
dc.subject | Arabidopsis Proteins | |
dc.subject | Base Sequence | |
dc.subject | Basic-leucine Zipper Transcription Factors | |
dc.subject | Binding Sites | |
dc.subject | Carrier Proteins | |
dc.subject | Gene Expression Regulation, Plant | |
dc.subject | Green Fluorescent Proteins | |
dc.subject | Molecular Sequence Data | |
dc.subject | Mutation | |
dc.subject | Nuclear Proteins | |
dc.subject | Plants, Genetically Modified | |
dc.subject | Promoter Regions, Genetic | |
dc.subject | Protein Binding | |
dc.subject | Salicylic Acid | |
dc.title | Functional Analysis Of A Tga Factor-binding Site Located In The Promoter Region Controlling Salicylic Acid-induced Nimin-1 Expression In Arabidopsis. | |
dc.type | Artículos de revistas | |