Coevolution of gene expression among interacting proteins

被引:172
作者
Fraser, HB
Hirsh, AE
Wall, DP
Eisen, MB
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
[3] Harvard Univ, Sch Med, Comp Biol Initiat, Boston, MA 02115 USA
[4] Lawrence Berkeley Lab, Dept Genome Sci, Berkeley, CA 92720 USA
[5] Harvard Univ, Dept Syst Biol, Boston, MA 02115 USA
关键词
D O I
10.1073/pnas.0402591101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Physically interacting proteins or parts of proteins are expected to evolve in a coordinated manner that preserves proper interactions. Such coevolution at the amino acid-sequence level is well documented and has been used to predict interacting proteins, domains, and amino acids. Interacting proteins are also often precisely coexpressed with one another, presumably to maintain proper stoichiometry among interacting components. Here, we show that the expression levels of physically interacting proteins coevolve. We estimate average expression levels of genes from four closely related fungi of the genus Saccharomyces using the codon adaptation index and show that expression levels of interacting proteins exhibit coordinated changes in these different species. We find that this coevolution of expression is a more powerful predictor of physical interaction than is coevolution of amino acid sequence. These results demonstrate that gene expression levels can coevolve, adding another dimension to the study of the coevolution of interacting proteins and underscoring the importance of maintaining coexpression of interacting proteins over evolutionary time. Our results also suggest that expression coevolution can be used for computational prediction of protein-protein interactions.
引用
收藏
页码:9033 / 9038
页数:6
相关论文
共 35 条
  • [1] Saccharomyces cerevisiae nucleolar protein Nop7p is necessary for biogenesis of 60S ribosomal subunits
    Adams, CC
    Jakovljevic, J
    Roman, J
    Harnpicharnchai, P
    Woolford, JL
    [J]. RNA, 2002, 8 (02) : 150 - 165
  • [2] Akashi H, 2003, GENETICS, V164, P1291
  • [3] CORRELATION OF COORDINATED AMINO-ACID SUBSTITUTIONS WITH FUNCTION IN VIRUSES RELATED TO TOBACCO MOSAIC-VIRUS
    ALTSCHUH, D
    LESK, AM
    BLOOMER, AC
    KLUG, A
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1987, 193 (04) : 693 - 707
  • [4] Genome-wide analysis of mRNA translation profiles in Saccharomyces cerevisiae
    Arava, Y
    Wang, YL
    Storey, JD
    Liu, CL
    Brown, PO
    Herschlag, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) : 3889 - 3894
  • [5] Predicting gene expression from sequence
    Beer, MA
    Tavazoie, S
    [J]. CELL, 2004, 117 (02) : 185 - 198
  • [6] Finding functional features in Saccharomyces genomes by phylogenetic footprinting
    Cliften, P
    Sudarsanam, P
    Desikan, A
    Fulton, L
    Fulton, B
    Majors, J
    Waterston, R
    Cohen, BA
    Johnston, M
    [J]. SCIENCE, 2003, 301 (5629) : 71 - 76
  • [7] Conservation of gene order: a fingerprint of proteins that physically interact
    Dandekar, T
    Snel, B
    Huynen, M
    Bork, P
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (09) : 324 - 328
  • [8] Discovery of uncharacterized cellular systems by genome-wide analysis of functional linkages
    Date, SV
    Marcotte, EM
    [J]. NATURE BIOTECHNOLOGY, 2003, 21 (09) : 1055 - 1062
  • [9] A large nucleolar U3 ribonucleoprotein required for 18S ribosomal RNA biogenesis
    Dragon, F
    Gallagher, JEG
    Compagnone-Post, PA
    Mitchell, BM
    Porwancher, KA
    Wehner, KA
    Wormsley, S
    Settlage, RE
    Shabanowitz, J
    Osheim, Y
    Beyer, AL
    Hunt, DF
    Baserga, SJ
    [J]. NATURE, 2002, 417 (6892) : 967 - 970
  • [10] Cluster analysis and display of genome-wide expression patterns
    Eisen, MB
    Spellman, PT
    Brown, PO
    Botstein, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) : 14863 - 14868