Matches in UGent Biblio for { <https://biblio.ugent.be/publication/192473#aggregation> ?p ?o. }
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- aggregation classification "A1".
- aggregation creator B74607.
- aggregation creator B74608.
- aggregation creator B74609.
- aggregation creator B74610.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation date "1995".
- aggregation format "application/pdf".
- aggregation hasFormat 192473.bibtex.
- aggregation hasFormat 192473.csv.
- aggregation hasFormat 192473.dc.
- aggregation hasFormat 192473.didl.
- aggregation hasFormat 192473.doc.
- aggregation hasFormat 192473.json.
- aggregation hasFormat 192473.mets.
- aggregation hasFormat 192473.mods.
- aggregation hasFormat 192473.rdf.
- aggregation hasFormat 192473.ris.
- aggregation hasFormat 192473.txt.
- aggregation hasFormat 192473.xls.
- aggregation hasFormat 192473.yaml.
- aggregation isPartOf urn:issn:0960-7412.
- aggregation language "eng".
- aggregation rights "I have transferred the copyright for this publication to the publisher".
- aggregation subject "Biology and Life Sciences".
- aggregation title "Differential in vitro DNA binding activity to a promoter element of the gn1 β-1,3-glucanase gene in hypersensitively reacting tobacco plants".
- aggregation abstract "In a hypersensitive reaction to pathogen infection, expression of the beta-1,3-glucanase gn1 gene is induced in cells surrounding the necrotic lesions. The 5'-flanking sequence of gn1 was examined to investigate the molecular basis controlling activation of gene expression during this plant defense response. Studies on transgenic tobacco plants containing gn1 promoter deletions fused to the beta-glucuronidase reporter gene revealed the presence of negative and positive regulatory sequences mediating both the level and the spatial distribution of gn1 expression. Promoter sequences to -138 bp were sufficient to confer increased gene expression around the necrotic lesions produced in response to Pseudomonas syringae pv. syringae inoculation. It is demonstrated by electrophoretic mobility shift assays that nuclear proteins in both healthy and hypersensitively reacting tobacco leaves interact with DNA sequences within the regulatory elements identified. Among the binding sequences characterized, the promoter region extending from -250 to -217 bp contained the DNA motif -GGCGGC- found to be conserved in most if not all promoters of genes encoding pathogenesis-related basic proteins. The activity bound by this promoter sequence was stronger in hypersensitively responding tissues than in healthy untreated tobacco leaves.".
- aggregation authorList BK190253.
- aggregation endPage "320".
- aggregation issue "2".
- aggregation startPage "309".
- aggregation volume "7".
- aggregation aggregates 4179904.
- aggregation isDescribedBy 192473.
- aggregation similarTo j.1365-313X.1995.7020309.x.
- aggregation similarTo LU-192473.