Literature DB >> 18810425

Natural selection in the TLR-related genes in the course of primate evolution.

Toshiaki Nakajima1, Hitoshi Ohtani, Yoko Satta, Yasuhiro Uno, Hirofumi Akari, Takafumi Ishida, Akinori Kimura.   

Abstract

The innate immune system constitutes the front line of host defense against pathogens. Toll-like receptors (TLRs) recognize molecules derived from pathogens and play crucial roles in the innate immune system. Here, we provide evidence that the TLR-related genes have come under natural selection pressure in the course of primate evolution. We compared the nucleotide sequences of 16 TLR-related genes, including TLRs (TLR1-10), MYD88, TILAP, TICAM1, TICAM2, MD2, and CD14, among seven primate species. Analysis of the non-synonymous/synonymous substitution ratio revealed the presence of both strictly conserved and rapidly evolving regions in the TLR-related genes. The genomic segments encoding the intracellular Toll/interleukin 1 receptor domains, which exhibited lower rates of non-synonymous substitution, have undergone purifying selection. In contrast, TLR4, which carried a high proportion of non-synonymous substitutions in the part of extracellular domain spanning 200 amino acids, was found to have been the suggestive target of positive Darwinian selection in primate evolution. However, sequence analyses from 25 primate species, including eight hominoids, six Old World monkeys, eight New World monkeys, and three prosimians, showed no evidence that the pressure of positive Darwinian selection has shaped the pattern of sequence variations in TLR4 among New World monkeys and prosimians.

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Year:  2008        PMID: 18810425     DOI: 10.1007/s00251-008-0332-0

Source DB:  PubMed          Journal:  Immunogenetics        ISSN: 0093-7711            Impact factor:   2.846


  22 in total

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2.  Codon-based tests of positive selection, branch lengths, and the evolution of mammalian immune system genes.

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3.  The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools.

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Journal:  Nat Immunol       Date:  2002-03-25       Impact factor: 25.606

5.  Positive Darwinian selection after gene duplication in primate ribonuclease genes.

Authors:  J Zhang; H F Rosenberg; M Nei
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-31       Impact factor: 11.205

6.  Species-specific recognition of single-stranded RNA via toll-like receptor 7 and 8.

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7.  Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene.

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Journal:  J Exp Med       Date:  1999-06-07       Impact factor: 14.307

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  26 in total

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2.  Distinct evolution of toll-like receptor signaling pathway genes in cetaceans.

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Journal:  Genes Genomics       Date:  2019-09-18       Impact factor: 1.839

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4.  Positive selection of Toll-like receptor 2 polymorphisms in two closely related old world monkey species, rhesus and Japanese macaques.

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Journal:  Immunogenetics       Date:  2011-07-09       Impact factor: 2.846

5.  Different selective pressures shape the evolution of Toll-like receptors in human and African great ape populations.

Authors:  Hélène Quach; Daniel Wilson; Guillaume Laval; Etienne Patin; Jeremy Manry; Jessica Guibert; Luis B Barreiro; Eric Nerrienet; Ernst Verschoor; Antoine Gessain; Molly Przeworski; Lluis Quintana-Murci
Journal:  Hum Mol Genet       Date:  2013-07-12       Impact factor: 6.150

6.  A history of recurrent positive selection at the toll-like receptor 5 in primates.

Authors:  Gabriela Wlasiuk; Soofia Khan; William M Switzer; Michael W Nachman
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8.  Comprehensive sequence analysis of the human IL23A gene defines new variation content and high rate of evolutionary conservation.

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9.  Signatures of positive selection in LY96 gene in vertebrates.

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Journal:  J Biosci       Date:  2013-12       Impact factor: 1.826

10.  Fast, adaptive evolution at a bacterial host-resistance locus: the PFam54 gene array in Borrelia burgdorferi.

Authors:  Ewa Wywial; James Haven; Sherwood R Casjens; Yozen A Hernandez; Shaneen Singh; Emmanuel F Mongodin; Claire M Fraser-Liggett; Benjamin J Luft; Steven E Schutzer; Wei-Gang Qiu
Journal:  Gene       Date:  2009-06-06       Impact factor: 3.688

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