Purifying selection and positive selection on the myxovirus resistance gene in mammals and chickens

被引:18
作者
Hou, Zhuo-Cheng
Xu, Gui-Yun
Su, Zhen
Yang, Ning [1 ]
机构
[1] China Agr Univ, Coll Anim Sci & Technol, Dept Anim Genet & Breeding, Beijing 100094, Peoples R China
[2] China Agr Univ, State Key Lab Agrobiotechnol, Beijing 100094, Peoples R China
[3] China Agr Univ, Coll Biol Sci, State Key Lab Plant Physiol & Biochem, Div Bioinformat, Beijing 100094, Peoples R China
关键词
Mx; adaptation; evolution; chicken; mammals;
D O I
10.1016/j.gene.2007.03.017
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The myxovirus resistance gene (Mx) expresses antiviral activity in many species, e.g. mouse, human and chicken. It is not clear if the antiviral activity of Mx has evolved in these species to inhibit a set of species-specific pathogens, nor what factors drive Mx evolution in different animal lineages. Therefore, it is important to determine the evolutionary pattern of Mx and positively selected sites which affect the antiviral activity of the Mx gene in mammals and birds. We used sequence comparisons among species to detect positively selected sites by conducting phylogenetic analysis. The two-ratio model was significantly better than the one-ratio model in four species (mouse, rat, chicken and duck, p < 0.05). Although selection pressure varied among different lineages, Mx had strong purifying selection in mammals and positive selection in chicken and duck lineages. Relative rate test revealed that Mx evolved faster in chickens than in ducks (Tajima's relative rate test, chi(2) =7.17,p < 0.01). In the further analysis using a branch-site model A test, 8 sites were positively selected in the chicken lineage while no positive selection signals were observed for any site in the other lineages. The branch-site model A test had a omega value of 4.374 for the chicken lineage (2 Delta C= 14.20, d.f. = 1, p < 0.001). Comparisons of all currently available Mx mRNA sequences showed that these predicted positively selected sites had been fixed in the chicken lineage, suggesting that the chicken Mx gene evolved within the species to resist newly challenging environments. There is an increased selection constraint leading to mammals, while positive selection has acted on the chicken Mx. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:188 / 195
页数:8
相关论文
共 48 条
[1]   NO ENHANCED INFLUENZA-VIRUS RESISTANCE OF MURINE AND AVIAN CELLS EXPRESSING CLONED DUCK MX PROTEIN [J].
BAZZIGHER, L ;
SCHWARZ, A ;
STAEHELI, P .
VIROLOGY, 1993, 195 (01) :100-112
[2]   THE INTERFERON-INDUCED MX-PROTEIN OF CHICKENS LACKS ANTIVIRAL ACTIVITY [J].
BERNASCONI, D ;
SCHULTZ, U ;
STAEHELI, P .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1995, 15 (01) :47-53
[3]   Differential transcriptional expresion of the polymorphic myxovirus resistance protein A in response to interferonalpha treatment [J].
Fernández-Arcás, N ;
Blanco, A ;
Gaitán, J ;
Nyqvist, M ;
Alonso, A ;
Reyes-Engel, A .
PHARMACOGENETICS, 2004, 14 (03) :189-193
[4]   Interferon-induced mx proteins: Dynamin-like GTPases with antiviral activity [J].
Haller, O ;
Kochs, G .
TRAFFIC, 2002, 3 (10) :710-717
[5]   Resolving the genetics of resistance to infectious diseases [J].
Hawken, RJ ;
Beattie, CW ;
Schook, LB .
REVUE SCIENTIFIQUE ET TECHNIQUE-OFFICE INTERNATIONAL DES EPIZOOTIES, 1998, 17 (01) :17-25
[6]   Dynamin and its role in membrane fission [J].
Hinshaw, JE .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2000, 16 :483-+
[7]   A SHARPER BONFERRONI PROCEDURE FOR MULTIPLE TESTS OF SIGNIFICANCE [J].
HOCHBERG, Y .
BIOMETRIKA, 1988, 75 (04) :800-802
[8]   A type I interferon signaling factor, ISF21, encoded on chromosome 21 is distinct from receptor components and their down-regulation and is necessary for transcriptional activation of interferon-regulated genes [J].
Holland, KA ;
Owczarek, CM ;
Hwang, SY ;
Tymms, MJ ;
Constantinescu, SN ;
Pfeffer, LM ;
Kola, I ;
Hertzog, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (34) :21045-21051
[9]   A regulatory role of c-Fos in the development of precursor B lymphocytes mediated by interleukin-7 [J].
Imoto, S ;
Hu, L ;
Tomita, Y ;
Phuchareon, J ;
Ruther, U ;
Tokuhisa, T .
CELLULAR IMMUNOLOGY, 1996, 169 (01) :67-74
[10]  
Ko JH, 2002, GENOME RES, V12, P595, DOI [10.1101/gr.210702, 10.1101/gr.210702. Article published online before print in March ]