Molecular cloning and characterization of a novel lectin gene from Lycoris radiata

DNA Seq. 2003 Jun;14(3):223-6. doi: 10.1080/1042517031000101716.

Abstract

By the use of RACE-PCR with RNA extracted from Lycoris radiata young leaves, the full-length cDNA of L. radiata agglutinin (LRA) was cloned. The full-length cDNA of LRA was 669 bp and contained a 477 bp open reading frame encoding a 158 amino acid protein. Through comparative analysis of lra gene and its deduced amino acid sequence with those of other Amaryllidaceae species, it was found that lra encoded a precursor lectin with signal peptide. LRA was a mannose-binding lectin with three mannose-binding boxes like lectins from other Amaryllidaceae species. Southern blot analysis of genomic DNA revealed that lra belonged to a low copy gene family. Northern blot analysis demonstrated that lra constitutively expressed in various plant tissues including leaf, root, stem and inflorescence, and highly expressed in the inflorescence.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Blotting, Northern
  • Blotting, Southern
  • DNA Primers
  • Gene Expression*
  • Lycoris / genetics*
  • Mannose-Binding Lectin / genetics*
  • Molecular Sequence Data
  • Sequence Alignment
  • Sequence Analysis, DNA

Substances

  • DNA Primers
  • Mannose-Binding Lectin

Associated data

  • GENBANK/AY191306