ArticleThe Plant cell1994
Promoter elements required for developmental expression of the maize Adh1 gene in transgenic rice.
Article in The Plant cell, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
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Who cites it
18 citing papers in PubMed, 53 citations in OpenAlex.
- Genomic Survey ofPlants (Basel, Switzerland) · 2022Article
- Temporal changes in transcripts of miniature inverted-repeat transposable elements during rice endosperm development.The Plant journal : for cell and molecular biology · 2022Article
- Circulating Epstein-Barr virus microRNA profile reveals novel biomarker for nasopharyngeal carcinoma diagnosis.Cancer biomarkers : section A of Disease markers · 2020Article
- The persimmon (Horticulture research · 2019Article
- The AP2/ERF transcription factor AtERF73/HRE1 modulates ethylene responses during hypoxia in Arabidopsis.Plant physiology · 2011Article
- Pollen-specific expression of Oryza sativa indica pollen allergen gene (OSIPA) promoter in rice and Arabidopsis transgenic systems.Molecular biotechnology · 2011Article
- Defining core metabolic and transcriptomic responses to oxygen availability in rice embryos and young seedlings.Plant physiology · 2009Article
- Differential expression of genes encoding 1-aminocyclopropane-1-carboxylate synthase in Arabidopsis during hypoxia.Plant molecular biology · 2005Article
- Rice ubiquitin promoters: deletion analysis and potential usefulness in plant transformation systems.Plant cell reports · 2003Article
- Conserved noncoding sequences among cultivated cereal genomes identify candidate regulatory sequence elements and patterns of promoter evolution.The Plant cell · 2003Article
- Down-regulation of caffeic acid o-methyltransferase in maize revisited using a transgenic approach.Plant physiology · 2002Article
- Signaling events in the hypoxic induction of alcohol dehydrogenase gene in Arabidopsis.Plant physiology · 2001Article
- Upstream and downstream sequence elements determine the specificity of the rice tungro bacilliform virus promoter and influence RNA production after transcription initiation.Plant molecular biology · 1999Article
- Mutations affecting induction of glycolytic and fermentative genes during germination and environmental stresses in Arabidopsis.Plant physiology · 1999Article
- The PR-1a promoter contains a number of elements that bind GT-1-like nuclear factors with different affinity.Plant molecular biology · 1996Article
- Regulation of expression of the cucumber isocitrate lyase gene in cotyledons upon seed germination and by sucrose.Plant molecular biology · 1995Article
- Aerobic fermentation in tobacco pollen.Plant molecular biology · 1995Article
- Pollen specificity elements reside in 30 bp of the proximal promoters of two pollen-expressed genes.The Plant cell · 1995Article
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5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
To define the regions of the maize alcohol dehydrogenase 1 (Adh1) promoter that confer tissue-specific expression, a series of 5' promoter deletions and substitution mutations were linked to the Escherichia coli beta-glucuronidase A (uidA) reporter gene and introduced into rice plants. A region between -140 and -99 not only conferred anaerobically inducible expression in the roots of transgenic plants but was also required for expression in the root cap, embryo, and in endosperm under aerobic conditions. GC-rich (GC-1, GC-2, and GC-3) or GT-rich (GT-1 and GT-2) sequence motifs in this region were necessary for expression in these tissues, as they were in anaerobic expression. Expression in the root cap under aerobic conditions required all the GC- and GT-rich motifs. The GT-1, GC-1, GC-2, and GC-3 motifs, and to a lesser extent the GT-2 motif, were also required for anaerobic responsiveness in rice roots. All elements except the GC-3 motif were needed for endosperm-specific expression. The GC-2 motif and perhaps the GT-1 motif appeared to be the only elements required for high-level expression in the embryos of rice seeds. Promoter regions important for shoot-, embryo-, and pollen-specific expression were proximal to -99, and nucleotides required for shoot-specific expression occurred between positions -72 and -43. Pollen-specific expression required a sequence element outside the promoter region, between +54 and +106 of the untranslated leader, as well as a silencer element in the promoter between -72 and -43.
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