The Arabidopsis USL1 controls multiple aspects of development by affecting late endosome morphology

New Phytol. 2018 Sep;219(4):1388-1405. doi: 10.1111/nph.15249. Epub 2018 Jun 13.

Abstract

The polar transport of auxin controls many aspects of plant development. However, the molecular mechanisms underlying auxin tranport regulation remain to be further elucidated. We identified a mutant named as usl1 (unflattened and small leaves) in a genetic screen in Arabidopsis thaliana. The usl1 displayed multiple aspects of developmental defects in leaves, embryogenesis, cotyledons, silique phyllotaxy and lateral roots in addition to abnormal leaves. USL1 encodes a protein orthologous to the yeast vacuolar protein sorting (Vps) 38p and human UV RADIATION RESISTANCE-ASSOCIATED GENE (UVRAG). Cell biology, Co-IP/MS and yeast two-hybrid were used to identify the function of USL1. USL1 colocalizes at the subcellular level with VPS29, a key factor of the retromer complex that controls auxin transport. The morphology of the VPS29-associated late endosomes (LE) is altered from small dots in the wild-type to aberrant enlarged circles in the usl1 mutants. The usl1 mutant synergistically interacts with vps29. We also found that USL1 forms a complex with AtVPS30 and AtVPS34. We propose that USL1 controls multiple aspects of plant development by affecting late endosome morphology and by regulating the PIN1 polarity. Our findings provide a new layer of the understanding on the mechanisms of plant development regulation.

Keywords: Arabidopsis thaliana; AtVPS30; AtVPS34 complex; USL1; VPS29; auxin transport; endocytic trafficking; late endosome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / genetics
  • Arabidopsis / growth & development*
  • Arabidopsis / metabolism*
  • Arabidopsis / ultrastructure
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Endocytosis
  • Endosomes / metabolism*
  • Endosomes / ultrastructure
  • Gene Expression Regulation, Plant
  • Genetic Pleiotropy
  • Genome, Plant
  • Membrane Transport Proteins
  • Models, Biological
  • Mutation / genetics
  • Organ Specificity / genetics
  • Phenotype
  • Phosphatidylinositol 3-Kinases / metabolism
  • Plant Development* / genetics
  • Protein Binding
  • Transcriptome / genetics
  • Vesicular Transport Proteins / genetics
  • Vesicular Transport Proteins / metabolism*

Substances

  • Arabidopsis Proteins
  • Membrane Transport Proteins
  • PIN1 protein, Arabidopsis
  • VPS38 protein, Arabidopsis
  • Vesicular Transport Proteins
  • Phosphatidylinositol 3-Kinases