Abstract |
A 33 bp double-stranded oligonucleotide homologous to two AT-rich sequences located upstream (-907 to -889 and -843 to -826) to the start of transcription of heat shock gene Gmhsp17.5E of soybean stimulated transcription when placed 5' to a truncated (-140) maize Adh1 promoter. The chimeric promoter was assayed in vivo utilizing anaerobically stressed sunflower tumors transformed by a pTi-based vector of Agrobacterium tumefaciens. Nuclear proteins extracted from soybean plumules were shown to bind double-stranded oligonucleotides homologous to AT-rich sequences in the 5' flanking regions of soybean beta-conglycinin, lectin, leghemoglobin and heat shock genes. These proteins were also shown to bind AT-rich probes homologous to homeobox protein binding sites from the Antennapedia and engrailed/fushi tarazu genes of Drosophila. Binding activity specific for AT-rich sequences showed a wide distribution among various plant organs and species. Preliminary characterization indicated that two sets of nuclear proteins from soybean bind AT-rich DNA sequences: a diverse high-molecular-weight (ca. 46-69 kDa) group, and a low-molecular-weight (23 and 32 kDa) group of proteins. The latter meets the operational criteria for high-mobility group proteins (HMGs).
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Authors | E Czarnecka, J C Ingersoll, W B Gurley |
Journal | Plant molecular biology
(Plant Mol Biol)
Vol. 19
Issue 6
Pg. 985-1000
(Sep 1992)
ISSN: 0167-4412 [Print] Netherlands |
PMID | 1511143
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Heat-Shock Proteins
- High Mobility Group Proteins
- Nuclear Proteins
- Alcohol Dehydrogenase
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Topics |
- Alcohol Dehydrogenase
(genetics)
- Base Composition
- Base Sequence
- Cloning, Molecular
- Heat-Shock Proteins
(genetics)
- High Mobility Group Proteins
(metabolism)
- Molecular Sequence Data
- Nuclear Proteins
(isolation & purification, metabolism)
- Promoter Regions, Genetic
(genetics)
- Glycine max
(genetics)
- Zea mays
(enzymology, genetics)
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