LbNrt RNA silencing in the mycorrhizal symbiont Laccaria bicolor reveals a nitrate-independent regulatory role for a eukaryotic NRT2-type nitrate transporter

Environ Microbiol Rep. 2013 Jun;5(3):353-66. doi: 10.1111/1758-2229.12029. Epub 2013 Jan 25.

Abstract

Fungal nitrogen metabolism plays a fundamental role in function of mycorrhizal symbiosis and consequently in nutrient cycling of terrestrial ecosystems. Despite its global ecological relevance the information on control and molecular regulation of nitrogen utilization in mycorrhizal fungi is very limited. We have extended the nitrate utilization RNA silencing studies of the model mycorrhizal basidiomycete, Laccaria bicolor, by altering the expression of LbNrt, the sole nitrate transporter-encoding gene of the fungus. Here we report the first nutrient transporter mutants for mycorrhizal fungi. Silencing of LbNrt results in fungal strains with minimal detectable LbNrt transcript levels, significantly reduced growth capacity on nitrate and altered symbiotic interaction with poplar. Transporter silencing also creates marked co-downregulation of whole Laccaria fHANT-AC (fungal high-affinity nitrate assimilation cluster). Most importantly, this effect on the nitrate utilization pathway appears independent of extracellular nitrate or nitrogen status of the fungus. Our results indicate a novel and central nitrate uptake-independent regulatory role for a eukaryotic nitrate transporter. The possible cellular mechanisms behind this regulation mode are discussed in the light of current knowledge on NRT2-type nitrate transporters in different eukaryotes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anion Transport Proteins / antagonists & inhibitors
  • Anion Transport Proteins / genetics*
  • Anion Transport Proteins / metabolism
  • Fungal Proteins / antagonists & inhibitors
  • Fungal Proteins / genetics*
  • Fungal Proteins / metabolism
  • Gene Expression Regulation, Fungal*
  • Laccaria / genetics*
  • Laccaria / metabolism
  • Mycorrhizae / genetics*
  • Mycorrhizae / metabolism
  • Nitrate Transporters
  • Nitrates / metabolism
  • Nitrogen / metabolism
  • Populus / microbiology
  • RNA Interference
  • RNA, Fungal / antagonists & inhibitors
  • RNA, Fungal / genetics*
  • RNA, Fungal / metabolism
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Symbiosis / physiology

Substances

  • Anion Transport Proteins
  • Fungal Proteins
  • Nitrate Transporters
  • Nitrates
  • RNA, Fungal
  • RNA, Small Interfering
  • Nitrogen