Molecular clock-like evolution of human immunodeficiency virus type 1

被引:12
作者
Liu, Y
Nickle, DC
Shriner, D
Jensen, MA
Learn, GH
Mittler, JE
Mullins, JI
机构
[1] Univ Washington, Sch Med, Dept Microbiol, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[3] Univ Washington, Sch Med, Dept Lab Med, Seattle, WA 98195 USA
关键词
molecular clock; HIV-1; natural selection; recombination;
D O I
10.1016/j.virol.2004.08.014
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The molecular clock hypothesis states that the rate of nucleotide substitution per generation is constant across lineages. If generation times were equal across lineages, samples obtained at the same calendar time would have experienced the same number of generations since their common ancestor. However, if sequences are not derived from contemporaneous samples, differences in the number of generations may be misinterpreted as variation in substitution rates and hence may lead to false rejection of the molecular clock hypothesis. A recent study has called into doubt the validity of clock-like evolution for HIV-1, using molecular sequences derived from noncontemporaneous samples. However, after separating their within-individual data according to sampling time, we found that what appeared to be nonclock-like behavior could be attributed, in most cases, to noncontemporaneous sampling, with contributions also likely to derive from recombination. Natural selection alone did not appear to obscure the clock-like evolution of HIV-1. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:101 / 108
页数:8
相关论文
共 62 条
[1]   Neutralism and selectionism: the molecular clock [J].
Ayala, FJ .
GENE, 2000, 261 (01) :27-33
[2]  
Beerli P, 1999, GENETICS, V152, P763
[3]   Maximum likelihood estimation of a migration matrix and effective population sizes in n subpopulations by using a coalescent approach [J].
Beerli, P ;
Felsenstein, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (08) :4563-4568
[4]   Antiviral pressure exerted by HIV-1-specific cytotoxic T lymphocytes (CTLs) during primary infection demonstrated by rapid selection of CTL escape virus [J].
Borrow, P ;
Lewicki, H ;
Wei, XP ;
Horwitz, MS ;
Peffer, N ;
Meyers, H ;
Nelson, JA ;
Gairin, JE ;
Hahn, BH ;
Oldstone, MBA ;
Shaw, GM .
NATURE MEDICINE, 1997, 3 (02) :205-211
[5]  
Burns D P, 1994, Curr Top Microbiol Immunol, V188, P185
[6]   HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 EVOLUTION IN-VIVO TRACKED BY DNA HETERODUPLEX MOBILITY ASSAYS [J].
DELWART, EL ;
SHEPPARD, HW ;
WALKER, BD ;
GOUDSMIT, J ;
MULLINS, JI .
JOURNAL OF VIROLOGY, 1994, 68 (10) :6672-6683
[7]   Reconstructing genealogies of serial samples under the assumption of a molecular clock using serial-sample UPGMA [J].
Drummond, A ;
Rodrigo, AG .
MOLECULAR BIOLOGY AND EVOLUTION, 2000, 17 (12) :1807-1815
[8]   EVOLUTIONARY TREES FROM DNA-SEQUENCES - A MAXIMUM-LIKELIHOOD APPROACH [J].
FELSENSTEIN, J .
JOURNAL OF MOLECULAR EVOLUTION, 1981, 17 (06) :368-376
[9]  
Fisher R. A., 1999, The Genetical Theory of Natural Selection: A Complete Variorum Edition
[10]   Evidence for positive selection driving the evolution of HIV-1 env under potent antiviral therapy [J].
Frost, SDW ;
Günthard, HF ;
Wong, JK ;
Havlir, D ;
Richman, DD ;
Brown, AJL .
VIROLOGY, 2001, 284 (02) :250-258