Molecular Genetics and Genomics

, Volume 283, Issue 5, pp 427–438

Unique evolutionary pattern of numbers of gramineous NBS–LRR genes

Original Paper

DOI: 10.1007/s00438-010-0527-6

Cite this article as:
Li, J., Ding, J., Zhang, W. et al. Mol Genet Genomics (2010) 283: 427. doi:10.1007/s00438-010-0527-6


Nucleotide binding site (NBS)–leucine-rich repeat (LRR) genes belong to the largest class of disease-resistance gene super groups in plants, and their intra- or interspecies nucleotide variations have been studied extensively to understand their evolution and function. However, little is known about the evolutionary patterns of their copy numbers in related species. Here, 129, 245, 239 and 508 NBSs were identified in maize, sorghum, brachypodium and rice, respectively, suggesting considerable variations of these genes. Based on phylogenetic relationships from a total of 496 ancestral branches of grass NBS families, three gene number variation patterns were categorized: conserved, sharing two or more species, and species-specific. Notably, the species-specific NBS branches are dominant (71.6%), while there is only a small percentage (3.83%) of conserved families. In contrast, the conserved families are dominant in 51 randomly selected house-keeping genes (96.1%). The opposite patterns between NBS and the other gene groups suggest that natural selection is responsible for the drastic number variation of NBS genes. The rapid expansion and/or contraction may be a fundamentally important strategy for a species to adapt to the quickly changing species-specific pathogen spectrum. In addition, the small proportion of conserved NBSs suggests that the loss of NBSs may be a general tendency in grass species.


NBS–LRR genes Copy number variation Adaptive evolution Gramineous species 

Supplementary material

438_2010_527_MOESM1_ESM.pdf (8.7 mb)
Supplementary Figure S1 (PDF 8,927 kb)
438_2010_527_MOESM2_ESM.pdf (106 kb)
Supplementary Tables S1–S5 (PDF 105 kb)

Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  • Jing Li
    • 1
  • Jing Ding
    • 1
  • Wen Zhang
    • 1
  • Yuanli Zhang
    • 1
  • Ping Tang
    • 1
  • Jian-Qun Chen
    • 1
  • Dacheng Tian
    • 1
  • Sihai Yang
    • 1
  1. 1.State Key Laboratory of Pharmaceutical Biotechnology, School of Life SciencesNanjing UniversityNanjingChina

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