ArticleEukaryotic cell2004
Core promoter structure in the oomycete Phytophthora infestans.
Article in Eukaryotic cell, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
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Who cites it
23 citing papers in PubMed.
- High-throughput time series expression profiling of Plasmopara halstedii infecting Helianthus annuus reveals conserved sequence motifs upstream of co-expressed genes.BMC genomics · 2023Article
- Alternative Transcription Start Site Usage and Functional Implications in Pathogenic Fungi.Journal of fungi (Basel, Switzerland) · 2022Review
- Conserved Subgroups of the Plant-Specific RWP-RK Transcription Factor Family Are Present in Oomycete Pathogens.Frontiers in microbiology · 2020Article
- Structural characterization of a putative chitin synthase gene in Phytophthora spp. and analysis of its transcriptional activity during pathogenesis on potato and soybean plants.Current genetics · 2017Article
- Characterization of marine diatom-infecting virus promoters in the model diatom Phaeodactylum tricornutum.Scientific reports · 2015Article
- PsMPK7, a stress-associated mitogen-activated protein kinase (MAPK) in Phytophthora sojae, is required for stress tolerance, reactive oxygenated species detoxification, cyst germination, sexual reproduction and infection of soybean.Molecular plant pathology · 2015Article
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- Genome-wide prediction and functional validation of promoter motifs regulating gene expression in spore and infection stages of Phytophthora infestans.PLoS pathogens · 2013Article
- Novel core promoter elements in the oomycete pathogen Phytophthora infestans and their influence on expression detected by genome-wide analysis.BMC genomics · 2013Article
- PsVPS1, a dynamin-related protein, is involved in cyst germination and soybean infection of Phytophthora sojae.PloS one · 2013Article
- Bioinformatic inference of specific and general transcription factor binding sites in the plant pathogen Phytophthora infestans.PloS one · 2012Article
- The CAZyome of Phytophthora spp.: a comprehensive analysis of the gene complement coding for carbohydrate-active enzymes in species of the genus Phytophthora.BMC genomics · 2010Article
- Characterization of cyclophilin-encoding genes in Phytophthora.Molecular genetics and genomics : MGG · 2009Article
- Regulation of catalase activity and gene expression during Phytophthora nicotianae development and infection of tobacco.Molecular plant pathology · 2008Article
- Phytophthora infestans: the plant (and R gene) destroyer.Molecular plant pathology · 2008Review
- Architecture of the sporulation-specific Cdc14 promoter from the oomycete Phytophthora infestans.Eukaryotic cell · 2007Article
- Performance of a tetracycline-responsive transactivator system for regulating transgenes in the oomycete Phytophthora infestans.Current genetics · 2007Article
- Nonneutral GC3 and retroelement codon mimicry in Phytophthora.Journal of molecular evolution · 2006Article
- Amplification generates modular diversity at an avirulence locus in the pathogen Phytophthora.Genome research · 2006Article
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3 authors.
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Abstract
We have investigated the core promoter structure of the oomycete Phytophthora infestans. The transcriptional start sites (TSS) of three previously characterized P. infestans genes, Piexo1, Piexo3, and Piendo1, were determined by primer extension analyses. The TSS regions were homologous to a previously identified 16-nucleotide (nt) core sequence that overlaps the TSS in most oomycete genes. The core promoter regions of Piexo1 and Piendo1 were investigated by using a transient protoplast expression assay and the reporter gene beta-glucuronidase. Mutational analyses of the promoters of Piexo1 and Piendo1 showed that there is a putative core promoter element encompassing the TSS (-2 to +5) that has high sequence and functional homology to a known core promoter element present in other eukaryotes, the initiator element (Inr). Downstream and flanking the Inr is a highly conserved oomycete promoter region (+7 to +15), hereafter referred to as FPR (flanking promoter region), which is also important for promoter function. The importance of the 19-nt core promoter region (Inr and FPR) in Piexo1 and Piendo1 was further investigated through electrophoretic mobility shift assays (EMSA). The EMSA studies showed that (i) both core promoters were able to specifically bind a protein or protein complex in a P. infestans whole-cell protein extract and (ii) the same mutations that reduced binding of the EMSA complex also reduced beta-glucuronidase (GUS) levels in transient expression assays. The consistency of results obtained using two different assays (GUS transient assays [in vivo] and EMSA studies [in vitro]) supports a convergence of inference about the relative importance of specific nucleotides within the 19-nt core promoter region.
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