Different models, different trees: The geographic origin of PTLV-I

被引:33
作者
Kelsey, CR
Crandall, KA [1 ]
Voevodin, AF
机构
[1] Brigham Young Univ, Dept Zool, Provo, UT 84602 USA
[2] Kuwait Univ, Fac Med, Dept Microbiol, Kuwait, Kuwait
基金
美国国家卫生研究院;
关键词
D O I
10.1006/mpev.1999.0663
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Using nucleotide sequences from three genomic regions of the human and simian T-cell lymphotropic virus type I (HTLV-I/STLV-I)-consisting of 69 sequences from a 140-bp segment of the pol region, 98 sequences from a 503-bp segment of the LTR, and 154 sequences from a 386-bp segment of the enu region-we tested two hypotheses concerning the geographic origin and evolution of STLV-I and HTLV-I, First, we tested the assumption of equal rates of evolution along STLV-I and HTLV-I lineages using a likelihood ratio test to ascertain whether current levels of genomic diversity can be used to determine ancestry. me demonstrated that unequal rates of evolution along HTLV-I and STLV-I lineages have occurred throughout evolutionary time, thus calling into question the use of pairwise distances to assign ancestry. Second, we constructed phylogenetic trees using multiple phylogenetic techniques to test for the geographic origin of STLV-I and HTLV-I. Using the principle of likelihood, we chose a statistically justified model of evolution for each data set. We demonstrated the utility of the likelihood ratio test to determine which model of evolution should be chosen for phylogenetic analyses, revealing that using different models of evolution produces conflicting results, and neither the hypothesis of an African origin nor the hypothesis of an Asian origin can be? rejected statistically. Our best estimates of phylogenetic relationships, however, support an African origin of PTLV for each gene region. (C) 1999 Academic Press.
引用
收藏
页码:336 / 347
页数:12
相关论文
共 50 条
[11]  
GESSAIN A, 1985, LANCET, V2, P407
[12]   The tax gene sequences form two divergent monophyletic lineages corresponding to types I and II of simian and human T-Cell leukemia lymphotropic viruses [J].
Giri, A ;
Slattery, JP ;
Heneine, W ;
Gessain, A ;
Rivadeneira, E ;
Desrosiers, RC ;
Rosen, L ;
Anthony, R ;
Pamungkas, J ;
Iskandriati, D ;
Richards, AL ;
Herve, V ;
McClure, H ;
OBrien, SJ ;
Franchini, G .
VIROLOGY, 1997, 231 (01) :96-104
[13]   NOVEL VIRAL SEQUENCES RELATED TO HUMAN T-CELL LEUKEMIA-VIRUS IN T-CELLS OF A SEROPOSITIVE BABOON [J].
GUO, HG ;
WONGSTAAL, F ;
GALLO, RC .
SCIENCE, 1984, 223 (4641) :1195-1197
[14]   DATING OF THE HUMAN APE SPLITTING BY A MOLECULAR CLOCK OF MITOCHONDRIAL-DNA [J].
HASEGAWA, M ;
KISHINO, H ;
YANO, TA .
JOURNAL OF MOLECULAR EVOLUTION, 1985, 22 (02) :160-174
[15]  
HUBBARD GB, 1993, LAB ANIM SCI, V43, P625
[16]   Phylogeny estimation and hypothesis testing using maximum likelihood [J].
Huelsenbeck, JP ;
Crandall, KA .
ANNUAL REVIEW OF ECOLOGY AND SYSTEMATICS, 1997, 28 :437-466
[17]   SUCCESS OF PHYLOGENETIC METHODS IN THE 4-TAXON CASE [J].
HUELSENBECK, JP ;
HILLIS, DM .
SYSTEMATIC BIOLOGY, 1993, 42 (03) :247-264
[18]  
JUKES TH, 1960, MAMMALIAN PROTEIN ME, P21
[19]   STRUCTURAL-ANALYSIS OF P19 AND P24 CORE POLYPEPTIDES OF PRIMATE LYMPHOTROPIC RETROVIRUSES (PLRV) [J].
JURKIEWICZ, E ;
NAKAMURA, H ;
SCHNEIDER, J ;
YAMAMOTO, N ;
HAYAMI, M ;
HUNSMANN, G .
VIROLOGY, 1986, 150 (01) :291-298
[20]   A NEW SUBTYPE OF HUMAN T-CELL LEUKEMIA-VIRUS (HTLV-II) ASSOCIATED WITH A T-CELL VARIANT OF HAIRY-CELL LEUKEMIA [J].
KALYANARAMAN, VS ;
SARNGADHARAN, MG ;
ROBERTGUROFF, M ;
MIYOSHI, I ;
BLAYNEY, D ;
GOLDE, D ;
GALLO, RC .
SCIENCE, 1982, 218 (4572) :571-573