The combination of a novel stimulatory element in the first exon of the maize Shrunken-1 gene with the following intron 1 enhances reporter gene expression up to 1000-fold

Plant Mol Biol. 1991 Feb;16(2):199-207. doi: 10.1007/BF00020552.

Abstract

Both exon 1 and intron 1 of the maize Shrunken-1 (Sh1) gene individually stimulate expression of reporter genes in transient gene expression experiments if present within the transcription unit. The Sh1 exon 1 mediates a 10-fold increase in activity when inserted at the 5' end of the bacterial chloramphenicol transacetylase (CAT) marker gene in both monocot and dicot protoplasts. The Sh1 intron 1 enhances chimeric gene expression in rice and maize protoplasts approximately 100-fold but inhibits CAT expression in tobacco protoplasts. In combination, the stimulatory effects of Sh1 exon 1 and intron 1 are multiplicative in monocot protoplasts resulting in a final enhancement of up to 1000-fold compared to the unmodified CAT or luciferase marker genes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Chloramphenicol O-Acetyltransferase / genetics
  • Cloning, Molecular / methods*
  • DNA*
  • Exons*
  • Genetic Markers / genetics
  • Introns
  • Luciferases / genetics
  • Molecular Sequence Data
  • Nicotiana / genetics
  • Plants, Toxic
  • Plasmids
  • Promoter Regions, Genetic
  • Protoplasts
  • Regulatory Sequences, Nucleic Acid*
  • Zea mays / genetics*

Substances

  • Genetic Markers
  • DNA
  • Luciferases
  • Chloramphenicol O-Acetyltransferase