Nucleotide diversity analysis of three major bacterial blight resistance genes in rice

PLoS One. 2015 Mar 25;10(3):e0120186. doi: 10.1371/journal.pone.0120186. eCollection 2015.

Abstract

Nucleotide sequence polymorphisms among R gene alleles influence the process of co-evolutionary interaction between host and pathogen by shaping the response of host plants towards invading pathogens. Here, we present the DNA sequence polymorphisms and diversities present among natural alleles of three rice bacterial blight resistance genes, Xa21, Xa26 and xa5. The diversity was examined across different wild relatives and cultivars of Oryza species. Functional significance of selected alleles was evaluated through semi-quantitative reverse transcription polymerase chain reaction and real time PCR. The greatest nucleotide diversity and singleton variable sites (SVS) were present in Xa26 (π = 0.01958; SVS = 182) followed by xa5 and Xa21 alleles. The highest frequency of single nucleotide polymorphisms were observed in Xa21 alleles and least in xa5. Transition bias was observed in all the genes and 'G' to 'A' transitions were more favored than other form of transitions. Neutrality tests failed to show the presence of selection at these loci, though negative Tajima's D values indicate the presence of a rare form of polymorphisms. At the interspecies level, O. nivara exhibited more diversity than O. sativa. We have also identified two nearly identical resistant alleles of xa5 and two sequentially identical alleles of Xa21. The alleles of xa5 showed basal levels of expression while Xa21 alleles were functionally not expressed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions
  • Alleles
  • DNA, Plant / analysis
  • Disease Resistance / genetics*
  • Evolution, Molecular
  • Genes, Plant*
  • Genetic Loci
  • Genetic Variation
  • Oryza / classification
  • Oryza / genetics*
  • Phylogeny
  • Plant Proteins / genetics
  • Polymorphism, Single Nucleotide
  • Real-Time Polymerase Chain Reaction
  • Sequence Analysis, DNA

Substances

  • 3' Untranslated Regions
  • DNA, Plant
  • Plant Proteins

Grants and funding

This research work is supported by grants from Department of Science & Technology, New Delhi, India (grant no. SR/SO/PS-21/09). WB is also grateful to CSIR for the fellowship (award no. 09/414/ (0832)/2008- EMR-I). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.