The yeast protein interaction network evolves rapidly and contains few redundant duplicate genes

被引:366
作者
Wagner, A
机构
[1] Univ New Mexico, Dept Biol, Albuquerque, NM 87131 USA
[2] Santa Fe Inst, Santa Fe, NM 87501 USA
关键词
protein network; evolution; Saccharomyces cerevisiae; yeast; gene duplication;
D O I
10.1093/oxfordjournals.molbev.a003913
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
In this paper, the structure and evolution of the protein interaction network of the yeast Saccharomyces cerevisiae is analyzed. The network is viewed as a graph whose nodes correspond to proteins Two proteins are connected by an edge if they interact. The network resembles a random graph in that it consists of many small subnets (groups of proteins that interact with each ether but do not interact with any other protein) and one large connected subnet comprising more than half of all interacting proteins. The number of interactions per protein appears to follow a power law distribution. Within approximately 200 Myr after a duplication, the products of duplicate genes become almost equally likely to (1) have common protein interaction partners and (2) be part of the same subnetwork as two proteins chosen at random from within the network. This indicates that the persistence of redundant interaction partners is the exception rather than the rule. After gene duplication, the likelihood that an interaction gets lost exceeds 2.2 X 10(-3)/Myr. New interactions are estimated to evolve at a rate that is approximately three orders of magnitude smaller. Every 300 Myr, as many as half of all interactions may be replaced by new interactions.
引用
收藏
页码:1283 / 1292
页数:10
相关论文
共 42 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   Phylogenetic reconstruction of vertebrate Hox cluster duplications [J].
Bailey, WJ ;
Kim, J ;
Wagner, GP ;
Ruddle, FH .
MOLECULAR BIOLOGY AND EVOLUTION, 1997, 14 (08) :843-853
[3]   Emergence of scaling in random networks [J].
Barabási, AL ;
Albert, R .
SCIENCE, 1999, 286 (5439) :509-512
[4]   A protein linkage map of Escherichia coli bacteriophage T7 [J].
Bartel, PL ;
Roecklein, JA ;
SenGupta, D ;
Fields, S .
NATURE GENETICS, 1996, 12 (01) :72-77
[5]  
BENNETZEN JL, 1982, J BIOL CHEM, V257, P3026
[6]   GENETIC-ANALYSIS OF CLN CDC28 REGULATION OF CELL MORPHOGENESIS IN BUDDING YEAST [J].
BENTON, BK ;
TINKELENBERG, AH ;
JEAN, D ;
PLUMP, SD ;
CROSS, FR .
EMBO JOURNAL, 1993, 12 (13) :5267-5275
[7]   Cla4p, a Saccharomyces cerevisiae Cdc42p-activated kinase involved in cytokinesis, is activated at mitosis [J].
Benton, BK ;
Tinkelenberg, A ;
Gonzalez, I ;
Cross, FR .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (09) :5067-5076
[8]  
Bollobas B, 1985, RANDOM GRAPHS
[9]   FUNCTIONAL REDUNDANCY - THE RESPECTIVE ROLES OF THE 2 SLOPPY PAIRED GENES IN DROSOPHILA SEGMENTATION [J].
CADIGAN, KM ;
GROSSNIKLAUS, U ;
GEHRING, WJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6324-6328
[10]   Molecular evolution of a duplication:: The sex-peptide (Acp70A) gene region of Drosophila subobscura and Drosophila madeirensis [J].
Cirera, S ;
Aguadé, M .
MOLECULAR BIOLOGY AND EVOLUTION, 1998, 15 (08) :988-996