Abstract
Our goal is to identify cis-acting elements in the regulatory region of the major seed storage protein gene in rice. A glutelin gene (pGL5-1) has been cloned by screening a rice genomic DNA library with synthetic oligonucleotides and with an amplified DNA fragment. A transient expression assay using immature rice seeds shows that its 5' flanking sequence can direct the synthesis of beta-glucuronidase (GUS) when fused upstream of the GUS coding region. Gel-retardation assays were performed to study protein-DNA interactions between putative regulatory sequences of pGL5-1 and nuclear proteins from immature rice seeds. We demonstrate that at least six protein-DNA complexes are formed between the 5' flanking sequence of pGL5-1 (-677 to -45) and nuclear protein factors. By subsequent DNase I-footprinting analyses we defined several protein-binding regions. Two of the protein-binding sequences contain the TGAGTCA motif, which is also present in the -300 element found in the 5' flanking sequences of several storage protein genes of other crop plants, and to which the transcription factors jun and GCN4 bind.
MeSH Terms
Base Sequence
Binding, Competitive
Cloning, Molecular
DNA-Binding Proteins/metabolism
Gene Expression Regulation
Glutens/genetics,metabolism
Molecular Sequence Data
Oligodeoxyribonucleotides/metabolism
Oryza/genetics
Promoter Regions, Genetic
Regulatory Sequences, Nucleic Acid
Restriction Mapping
Sequence Homology, Nucleic Acid
Chemicals
DNA-Binding Proteins
Oligodeoxyribonucleotides
Glutens
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kim S Y
Section of Biochemistry, Molecular and Cell Biology, Cornell University, Ithaca, NY 14853.
Wu R
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