RNAi-suppression of barley caffeic acid O-methyltransferase modifies lignin despite redundancy in the gene family

Plant Biotechnol J. 2019 Mar;17(3):594-607. doi: 10.1111/pbi.13001. Epub 2018 Oct 2.

Abstract

Caffeic acid O-methyltransferase (COMT), the lignin biosynthesis gene modified in many brown-midrib high-digestibility mutants of maize and sorghum, was targeted for downregulation in the small grain temperate cereal, barley (Hordeum vulgare), to improve straw properties. Phylogenetic and expression analyses identified the barley COMT orthologue(s) expressed in stems, defining a larger gene family than in brachypodium or rice with three COMT genes expressed in lignifying tissues. RNAi significantly reduced stem COMT protein and enzyme activity, and modestly reduced stem lignin content while dramatically changing lignin structure. Lignin syringyl-to-guaiacyl ratio was reduced by ~50%, the 5-hydroxyguaiacyl (5-OH-G) unit incorporated into lignin at 10--15-fold higher levels than normal, and the amount of p-coumaric acid ester-linked to cell walls was reduced by ~50%. No brown-midrib phenotype was observed in any RNAi line despite significant COMT suppression and altered lignin. The novel COMT gene family structure in barley highlights the dynamic nature of grass genomes. Redundancy in barley COMTs may explain the absence of brown-midrib mutants in barley and wheat. The barley COMT RNAi lines nevertheless have the potential to be exploited for bioenergy applications and as animal feed.

Keywords: Biofuels; barley (Hordeum vulgare); brown-midrib; caffeic acid O-methyltransferase (COMT); lignin; straw.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Gene Expression Regulation, Plant / genetics
  • Genes, Plant / genetics
  • Hordeum / enzymology
  • Hordeum / genetics
  • Hordeum / metabolism*
  • Lignin / metabolism*
  • Methyltransferases / metabolism*
  • Phylogeny
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • RNA Interference*

Substances

  • Plant Proteins
  • Lignin
  • Methyltransferases
  • caffeate O-methyltransferase