Four distinct nuclear proteins recognize in vitro the proximal promoter of the bean seed storage protein beta-phaseolin gene conferring spatial and temporal control

Plant J. 1992 Nov;2(6):927-36. doi: 10.1046/j.1365-313x.1992.t01-6-00999.x.

Abstract

A proximal promoter (-422/-13) of the bean seed storage protein beta-phaseolin gene contains cis-regulatory elements conferring spatial and temporal gene regulation. To correlate trans-acting elements with these cis-elements, we performed gel mobility shift and exonuclease III protection assays using bean seed nuclear proteins, and identified target sequences of four DNA-binding proteins associated with this promoter. Three CANNTG motifs, CACGTG (-248/-243), CACCTG (-163/-158), and CATATG (-100/-95), were determined as target sequences of the same DNA-binding protein designated CAN. Competition assays using oligonucleotides containing the wild-type or mutated CANNTG motif indicated that the CANNTG motif appears to be a preferred target sequence for CAN binding. Competition assays also demonstrated that DNA-binding protein AG-1 binds to AAAAAG(A/G)CAA (-356/-347, -191/-182), CA-1 binds to two CA-rich sequences (-201/-192, -175/-160), and that a TATA-box binding protein binds to either TATATAA (-43/-37) or TATAAA (-32/-27) or both. Based on these and other results, it is proposed that CACGTG motif (-248/-243) is a major cis-acting regulatory element conferring spatial and temporal control of the beta-phaseolin gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Binding, Competitive
  • DNA-Binding Proteins / metabolism*
  • Exodeoxyribonucleases / metabolism
  • Fabaceae / genetics*
  • Genes, Plant / genetics*
  • Models, Genetic
  • Molecular Sequence Data
  • Nuclear Proteins / metabolism
  • Plant Proteins / genetics*
  • Plants, Medicinal*
  • Promoter Regions, Genetic / genetics*
  • Restriction Mapping
  • Transcription, Genetic

Substances

  • DNA-Binding Proteins
  • Nuclear Proteins
  • Plant Proteins
  • phaseolin protein, Phaseolus vulgaris
  • Exodeoxyribonucleases
  • exodeoxyribonuclease III