Computational and statistical methods to explore the various dimensions of protein evolution

被引:12
作者
Fares, Mario A. [1 ]
机构
[1] Natl Univ Ireland, Mol Evolut & Bioinformat Lab, Dept Biol, Maynooth, Kildare, Ireland
关键词
adaptive evolution; coevolution; statistical methods; maximum likelihood; parsimony; covarion model;
D O I
10.2174/157489306777011950
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Predicting genes and gene regions undergoing adaptive evolution is one of the most important aims of geneticists and of new emerging areas of investigation. As more genomes are being sequenced and computational tools to detect selection are being developed, the number of genes uncovered as being positively selected is overwhelming. Several statistical methods have been devised to test if specific amino acid regions have undergone adaptive mutations at some stage during the protein's evolution. Despite the sensitivity of these methods to detect selective constraints, they are still based on linear sequence alignments and therefore, examine only one dimension of the protein's evolution. Few methods have been designed to detect intra-molecular co-evolution between amino acid sites. However, no tests are performed to determine the adaptive value of these co-evolutionary events. Conclusions independently derived from both types of methods are ambiguous and seldom unequivocal, since evolution of protein sequences is most likely to be multifactorial. This review discusses and has briefly exposed the advantages and disadvantages of the many different methods and computational tools to detect adaptive evolution and co-evolution. Further, the potential that the combination of such methods has in providing more biologically meaningful results is highlighted.
引用
收藏
页码:207 / 217
页数:11
相关论文
共 128 条
[1]   Within- and between-species DNA sequence variation and the 'footprint' of natural selection [J].
Akashi, H .
GENE, 1999, 238 (01) :39-51
[2]   Phylogenetically enhanced statistical tools for RNA structure prediction [J].
Akmaev, VR ;
Kelley, ST ;
Stormo, GD .
BIOINFORMATICS, 2000, 16 (06) :501-512
[3]   CORRELATION OF COORDINATED AMINO-ACID SUBSTITUTIONS WITH FUNCTION IN VIRUSES RELATED TO TOBACCO MOSAIC-VIRUS [J].
ALTSCHUH, D ;
LESK, AM ;
BLOOMER, AC ;
KLUG, A .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 193 (04) :693-707
[4]   Covarion structure in plastid genome evolution:: A new statistical test [J].
Ané, C ;
Burleigh, JG ;
McMahon, MM ;
Sanderson, MJ .
MOLECULAR BIOLOGY AND EVOLUTION, 2005, 22 (04) :914-924
[5]  
[Anonymous], 1991, The Causes of Molecular Evolution
[6]   Statistical properties of neutral evolution [J].
Bastolla, U ;
Porto, M ;
Roman, HE ;
Vendruscolo, M .
JOURNAL OF MOLECULAR EVOLUTION, 2003, 57 (Suppl 1) :S103-S119
[7]   How to guarantee optimal stability for most representative structures in the protein data bank [J].
Bastolla, U ;
Farwer, J ;
Knapp, EW ;
Vendruscolo, M .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 2001, 44 (02) :79-96
[8]   Structurally constrained protein evolution: results from a lattice simulation [J].
Bastolla, U ;
Vendruscolo, M ;
Roman, HE .
EUROPEAN PHYSICAL JOURNAL B, 2000, 15 (02) :385-397
[9]   GENETICS, PHYSIOLOGY, AND EVOLUTIONARY RELATIONSHIPS OF THE GENUS BUCHNERA - INTRACELLULAR SYMBIONTS OF APHIDS [J].
BAUMANN, P ;
BAUMANN, L ;
LAI, CY ;
ROUBAKHSH, D ;
MORAN, NA ;
CLARK, MA .
ANNUAL REVIEW OF MICROBIOLOGY, 1995, 49 :55-94
[10]   Tertiary windowing to detect positive diversifying selection [J].
Berglund, AC ;
Wallner, B ;
Elofsson, A ;
Liberles, DA .
JOURNAL OF MOLECULAR EVOLUTION, 2005, 60 (04) :499-504