s'authentifier
version française rss feed
Signatures of positive selection in Toll-like receptor (TLR) genes in mammals.
Areal H., Abrantes J., Esteves P.
BMC Evolutionary Biology 11, 1 (2011) 368 - http://www.hal.inserm.fr/inserm-00668409
 (22185391) 
Signatures of positive selection in Toll-like receptor (TLR) genes in mammals.
Helena Areal1, 2, Joana Abrantes1, 3, Pedro Esteves () 1, 4
1 :  CIBIO-UP
Universidade do Porto
Centro de Investigacao em Biodiversidade e Recursos Geneticos - Campus Agrario de Vairao, Rua Padre Armando Quintas, nr.7, 4485-661 Vairao
Portugal
2 :  Departamento de Zoologia e Antropologia
Universidade do Porto
Faculdade de Ciencias, Porto
Portugal
3 :  CRCNA - Centre de Recherche en Cancérologie Nantes - Angers
INSERM : U892 – Université de Nantes
France
4 :  CITS
Centro de Investigacao em Tecnologias de Saude
CESPU, Gandra
Portugal
UNLABELLED: ABSTRACT: BACKGROUND: Toll-like receptors (TLRs) are a major class of pattern recognition receptors (PRRs) expressed in the cell surface or membrane compartments of immune and non-immune cells. TLRs are encoded by a multigene family and represent the first line of defense against pathogens by detecting foreigner microbial molecular motifs, the pathogen-associated molecular patterns (PAMPs). TLRs are also important by triggering the adaptive immunity in vertebrates. They are characterized by the presence of leucine-rich repeats (LRRs) in the ectodomain, which are associated with the PAMPs recognition. The direct recognition of different pathogens by TLRs might result in different evolutionary adaptations important to understand the dynamics of the host-pathogen interplay. Ten mammal TLR genes, viral (TLR3, 7, 8, 9) and non-viral (TLR1-6, 10), were selected to identify signatures of positive selection that might have been imposed by interacting pathogens and to clarify if viral and non-viral TLRs might display different patterns of molecular evolution. RESULTS: By using Maximum Likelihood approaches, evidence of positive selection was found in all the TLRs studied. The number of positively selected codons (PSC) ranged between 2-26 codons (0.25%-2.65%) with the non-viral TLR4 as the receptor with higher percentage of positively selected codons (2.65%), followed by the viral TLR8 (2.50%). The results indicated that viral and non-viral TLRs are similarly under positive selection. Almost all TLRs have at least one PSC located in the LRR ectodomain which underlies the importance of the pathogen recognition by this region. CONCLUSIONS: Our results are not in line with previous studies on primates and birds that identified more codons under positive selection in non-viral TLRs. This might be explained by the fact that both primates and birds are homogeneous groups probably being affected by only a restricted number of related viruses with equivalent motifs to be recognized. The analyses performed in this work encompassed a large number of species covering some of the most representative mammalian groups - Artiodactyla, Rodents, Carnivores, Lagomorphs and Primates - that are affected by different families of viruses. This might explain the role of adaptive evolution in shaping viral TLR genes.
Sciences de l'environnement/Biodiversité et Ecologie
Sciences du Vivant/Sciences agricoles
Sciences du Vivant/Génétique
Anglais
1471-2148

Articles dans des revues avec comité de lecture
10.1186/1471-2148-11-368
BMC Evolutionary Biology (BMC Evol Biol)
Publisher BioMed Central
ISSN 1471-2148 
internationale
2011
20/12/2011
11
1
368

The Portuguese Foundation for Science and Technology supported the doctoral fellowship of Helena Areal (SFRH/BD/74948/2010) and the post-doctoral fellowships of Joana Abrantes (SFRH/BPD/73512/2010) and Pedro J. Esteves (SPRH/BPD/27021/2006).
Liste des fichiers attachés à ce document : 
PDF
1471-2148-11-368.pdf(2 MB)
ANNEX
1471-2148-11-368.xml(141.1 KB)
1471-2148-11-368-S30.DOC(227.5 KB)
1471-2148-11-368-S1.DOC(104 KB)
1471-2148-11-368-S13.DOC(290.5 KB)
1471-2148-11-368-S8.DOC(106 KB)
1471-2148-11-368-S16.DOC(150.5 KB)
1471-2148-11-368-S19.DOC(180.5 KB)
1471-2148-11-368-S32.DOC(246.5 KB)
1471-2148-11-368-S23.DOC(250 KB)
1471-2148-11-368-S37.DOC(228 KB)
1471-2148-11-368-S3.DOC(113 KB)
1471-2148-11-368-S18.DOC(212.5 KB)
1471-2148-11-368-S29.DOC(262.5 KB)
1471-2148-11-368-S7.DOC(117.5 KB)
1471-2148-11-368-S36.DOC(138 KB)
1471-2148-11-368-S24.DOC(244 KB)
1471-2148-11-368-S27.DOC(260.5 KB)
1471-2148-11-368-S14.DOC(203 KB)
1471-2148-11-368-S25.DOC(239 KB)
1471-2148-11-368-S26.DOC(223.5 KB)
1471-2148-11-368-S22.DOC(226.5 KB)
1471-2148-11-368-S38.DOC(376 KB)
1471-2148-11-368-S5.DOC(108.5 KB)
1471-2148-11-368-S4.DOC(109.5 KB)
1471-2148-11-368-S20.DOC(183 KB)
1471-2148-11-368-S33.DOC(261 KB)
1471-2148-11-368-S28.DOC(272 KB)
1471-2148-11-368-S21.DOC(225 KB)
1471-2148-11-368-S10.DOC(89.5 KB)
1471-2148-11-368-S35.DOC(248 KB)
1471-2148-11-368-S39.DOC(157 KB)
1471-2148-11-368-S9.DOC(116 KB)
1471-2148-11-368-S17.DOC(262 KB)
1471-2148-11-368-S15.DOC(209 KB)
1471-2148-11-368-S11.DOC(115.5 KB)
1471-2148-11-368-S2.DOC(124 KB)
1471-2148-11-368-S40.DOC(204.5 KB)
1471-2148-11-368-S34.DOC(342.5 KB)
1471-2148-11-368-S12.DOC(255.5 KB)
1471-2148-11-368-S31.DOC(104 KB)
1471-2148-11-368-S6.DOC(114 KB)

tous les articles de la base du CCSd...