Polymorphism distribution and structural conservation in RNA-sensing Toll-like receptors 3, 7, and 8 in pigs

Biochim Biophys Acta. 2009 Apr;1790(4):267-74. doi: 10.1016/j.bbagen.2009.01.002.

Abstract

Background: Viral genomic RNA-both single-stranded (ss) and double-stranded (ds)-is recognized by RNA-sensing Toll-like receptors (TLRs), notably TLR3 (dsRNA), TLR7 (ssRNA), and TLR8 (ssRNA). However, our knowledge of the roles of porcine TLR3, 7, and 8 in antiviral immunity is inadequate.

Methods: From information on exon-intron boundaries obtained through comparisons of the genomic and cDNA sequences, polymorphisms in the coding sequences of each gene were detected in 84 male pigs of 11 breeds.

Results: Genomic structures are conserved between pigs and humans. The RNA-sensing TLR genes had fewer polymorphisms causing amino acid alterations than did the cell-surface TLR genes, but the alterations were distributed with a similar bias toward ectodomains.

Conclusions: The low level of diversity of substitutive polymorphisms in RNA-sensing TLRs than cell-surface ones implies that polymorphisms severely affecting function have been eliminated by selection pressure during longstanding pig breeding.

General significance: Recognition of virus-derived RNA is critical in host defense against infection. These results should provide a useful clue to analysis of the association between polymorphisms in RNA-sensing TLRs and disease resistance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Conserved Sequence
  • Humans
  • Male
  • Phylogeny
  • Polymorphism, Single Nucleotide
  • RNA, Viral / genetics
  • Sus scrofa / genetics*
  • Toll-Like Receptor 3 / genetics*
  • Toll-Like Receptor 7 / genetics*
  • Toll-Like Receptor 8 / genetics*

Substances

  • RNA, Viral
  • Toll-Like Receptor 3
  • Toll-Like Receptor 7
  • Toll-Like Receptor 8