The transcriptomic landscapes of rice cultivars with diverse root system architectures grown in upland field conditions

Plant J. 2021 May;106(4):1177-1190. doi: 10.1111/tpj.15226. Epub 2021 Apr 5.

Abstract

Root system architecture affects plant drought resistance and other key agronomic traits such as lodging. However, although phenotypic and genomic variation has been extensively analyzed, few field studies have integrated phenotypic and transcriptomic information, particularly for below-ground traits such as root system architecture. Here, we report the phenotypic and transcriptomic landscape of 61 rice (Oryza sativa) accessions with highly diverse below-ground traits grown in an upland field. We found that four principal components explained the phenotypic variation and that accessions could be classified into four subpopulations (indica, aus, japonica and admixed) based on their tiller numbers and crown root diameters. Transcriptome analysis revealed that differentially expressed genes associated with specific subpopulations were enriched with stress response-related genes, suggesting that subpopulations have distinct stress response mechanisms. Root growth was negatively correlated with auxin-inducible genes, suggesting an association between auxin signaling and upland field conditions. A negative correlation between crown root diameter and stress response-related genes suggested that thicker crown root diameter is associated with resistance to mild drought stress. Finally, co-expression network analysis implemented with DNA affinity purification followed by sequencing analysis identified phytohormone signaling networks and key transcription factors negatively regulating crown root diameter. Our datasets provide a useful resource for understanding the genomic and transcriptomic basis of phenotypic variation under upland field conditions.

Keywords: diversity; drought stress; field transcriptomes; rice; root system architecture; transcription factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Droughts
  • Gene Expression Profiling
  • Indoleacetic Acids / metabolism*
  • Oryza / genetics*
  • Oryza / physiology
  • Phenotype
  • Plant Growth Regulators / metabolism*
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Plant Roots / genetics
  • Plant Roots / physiology
  • Stress, Physiological
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcriptome*

Substances

  • Indoleacetic Acids
  • Plant Growth Regulators
  • Plant Proteins
  • Transcription Factors