Abstract

Most disease resistance genes encode nucleotide-binding-site (NBS) and leucine-rich-repeat (LRR) domains, and the NBS-LRR encoding genes are often referred to as R genes. Using newly developed approach, 478, 485, 1,194, 1,665, 2,042 and 374 R genes were identified from the genomes of tomato Heinz1706, wild tomato LA716, potato DM1-3, pepper Zunla-1 and wild pepper Chiltepin and tobacco TN90, respectively. The majority of R genes from Solanaceae were grouped into 87 subfamilies, including 16 TIR-NBS-LRR (TNL) and 71 non-TNL subfamilies. Each subfamily was annotated manually, including identification of intron/exon structure and intron phase. Interestingly, TNL subfamilies have similar intron phase patterns, while the non-TNL subfamilies have diverse intron phase due to frequent gain of introns. Prevalent presence/absence polymorphic R gene loci were found among Solanaceae species, and an integrated map with 427 R loci was constructed. The pepper genome (2,042 in Chiltepin) has at least four times of R genes as in tomato (478 in Heinz1706). The high number of R genes in pepper genome is due to the amplification of R genes in a few subfamilies, such as the Rpi-blb2 and BS2 subfamilies. The mechanism underlying the variation of R gene number among different plant genomes is discussed.

Highlights

  • Plants harbor a variety of disease resistance genes to protect themselves from their natural enemies, such as pests, viruses and fungi

  • Compared with previous studies [14,15], 121 and 450 additional R genes were obtained from the genomes of tomato Heinz1706 and potato DM1-3 (S1 Table)

  • A species-specific NBS domain Hidden Markov Model (HMM) profile was first constructed using hmmbuild implemented in the HMMER software

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Summary

Introduction

Plants harbor a variety of disease resistance genes to protect themselves from their natural enemies, such as pests, viruses and fungi. More than 140 resistance genes have been cloned and well characterized from flowering plants, of which approximately 80% encode nucleotide-binding-site (NBS) and leucine-rich-repeat (LRR) domains [1,2,3]. The NBS-LRR encoding genes belong to a large gene family, with hundreds of copies in a genome [4,5,6]. Based on their N-terminal structures, these R proteins can be further divided into two subclasses: TIR-NBS-LRR (TNL) that possesses a domain homologous to the Toll and interleukin receptor (TIR), and non-TNL. Most non-TNL R proteins have a coiled-coil (CC) structure at PLOS ONE | DOI:10.1371/journal.pone.0148708 February 5, 2016

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