1989
DOI: 10.1007/bf00036973
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Isolation and sequence of a genomic clone encoding the basic form of pathogenesis-related protein 1 fromNicotiana tabacum

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Cited by 44 publications
(33 citation statements)
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“…They exhibited differential antifungal activity in vitro and in vivo (leaf disc assay) toward P. infestam. The protein with the higher antifungal activity, P14c, showed only low sequence similarity (65%) to the initially described P14 (Lucas et al, 1985) but high similarity (94%) to the basic tobacco PR-1 predicted from a cDNA clone (Cornelissen et al, 1987) and from genomic DNA clones (Payne et al, 1989;Eyal et al, 1992). This putative basic PR protein, named PR-lg, was then isolated from tobacco leaves reacting hypersensitively to tobacco mosaic virus, along with the three well-known acidic proteins PR-la, PR-lb, and PR-lc.…”
mentioning
confidence: 88%
See 1 more Smart Citation
“…They exhibited differential antifungal activity in vitro and in vivo (leaf disc assay) toward P. infestam. The protein with the higher antifungal activity, P14c, showed only low sequence similarity (65%) to the initially described P14 (Lucas et al, 1985) but high similarity (94%) to the basic tobacco PR-1 predicted from a cDNA clone (Cornelissen et al, 1987) and from genomic DNA clones (Payne et al, 1989;Eyal et al, 1992). This putative basic PR protein, named PR-lg, was then isolated from tobacco leaves reacting hypersensitively to tobacco mosaic virus, along with the three well-known acidic proteins PR-la, PR-lb, and PR-lc.…”
mentioning
confidence: 88%
“…Protein PR-lg was predicted from sequence data (Cornelissen et al, 1987;Payne et al, 1989;13yal et al, 1992) to be a basic protein. Therefore, we used a procedure similar to the one that allowed the isolation of c ther basic tobacco PR proteins (Geoffroy et al, 1990;Heitz et al, 1994b).…”
Section: Purification Of Tobacco Pr-1 Proteinsmentioning
confidence: 99%
“…The PR-1-related cDNA was isolated by cross-hybridization to tobacco PR-1 acidic and basic cDNAs at low stringency (Payne et al, 1988b(Payne et al, , 1989. The sequence of the longest of three identical clones is shown in Figure 5A.…”
Section: Biological Responses Of Arabidopsis To Chemical Lmmunizationmentioning
confidence: 99%
“…The Arabidopsis PR-1 cDNA was isolated by screening the cDNA library at low stringency with a mixture of both the PR-la (Payne et al, 1988b) and PR-lbasic (Payne et al, 1989) cDNAs from tobacco as probes. The cDNA library was plated at 5000 plaque-forming units per plate, and filter lifts were taken with nitrocellulose filters (Ausubel et al, 1987).…”
Section: Pr-5 Proteinmentioning
confidence: 99%
“…PR-1 genes are expressed due to various external stimuli like pathogens, injury, chemical elicitors, hormones, UV light (9) and salicylic acid. PR-1 proteins contain a hydrophobic N-terminal region of 30 amino acids that probably function as a signal peptide for the translocation to the endoplasmic reticulum (38). The FORESTs database has sequences (EGSBRT3122B04.g and EGBMCL1291G04.g) similar to C. annum PR-1 and a precursor protein of maize, respectively (Table 5).…”
Section: Pathogenesis-related Proteins (Pr-proteins)mentioning
confidence: 99%