Multiple protein factors bind to a rice glutelin promoter region

Nucleic Acids Res. 1990 Dec 11;18(23):6845-52. doi: 10.1093/nar/18.23.6845.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Binding, Competitive
  • Cloning, Molecular
  • DNA-Binding Proteins / metabolism*
  • Gene Expression Regulation*
  • Glutens / genetics*
  • Glutens / metabolism
  • Molecular Sequence Data
  • Oligodeoxyribonucleotides / metabolism
  • Oryza / genetics*
  • Promoter Regions, Genetic*
  • Regulatory Sequences, Nucleic Acid
  • Restriction Mapping
  • Sequence Homology, Nucleic Acid

Substances

  • DNA-Binding Proteins
  • Oligodeoxyribonucleotides
  • Glutens

Associated data

  • GENBANK/X52153