Following Gene Duplication, Paralog Interference Constrains Transcriptional Circuit Evolution

被引:88
作者
Baker, Christopher R. [1 ,2 ]
Hanson-Smith, Victor [1 ,2 ]
Johnson, Alexander D. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Immunol & Microbiol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
关键词
DNA-BINDING; BOX PROTEIN; ARGININE; MCM1; SPECIFICITY; METABOLISM; COFACTORS;
D O I
10.1126/science.1240810
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
Most models of gene duplication assume that the ancestral functions of the preduplication gene are independent and can therefore be neatly partitioned between descendant paralogs. However, many gene products, such as transcriptional regulators, are components within cooperative assemblies; here, we show that a natural consequence of duplication and divergence of such proteins can be competitive interference between the paralogs. Our example is based on the duplication of the essential MADS-box transcriptional regulator Mcm1, which is found in all fungi and regulates a large set of genes. We show that a set of historical amino acid sequence substitutions minimized paralog interference in contemporary species and, in doing so, increased the molecular complexity of this gene regulatory network. We propose that paralog interference is a common constraint on gene duplicate evolution, and its resolution, which can generate additional regulatory complexity, is needed to stabilize duplicated genes in the genome.
引用
收藏
页码:104 / 108
页数:5
相关论文
共 23 条
[1]   Scanning mutagenesis of Mcm1: Residues required for DNA binding, DNA bending, and transcriptional activation by a MADS-box protein [J].
Acton, TB ;
Mead, J ;
Steiner, AM ;
Vershon, AK .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (01) :1-11
[2]   ArgRII, a component of the ArgR-Mcm1 complex involved in the control of arginine metabolism in Saccharomyces cerevisiae, is the sensor of arginine [J].
Amar, N ;
Messenguy, F ;
El Bakkoury, M ;
Dubois, E .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (06) :2087-2097
[3]   Extensive DNA-binding specificity divergence of a conserved transcription regulator [J].
Baker, Christopher R. ;
Tuch, Brian B. ;
Johnson, Alexander D. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (18) :7493-7498
[4]   MAT-ALPHA-1 PROTEIN, A YEAST TRANSCRIPTION ACTIVATOR, BINDS SYNERGISTICALLY WITH A 2ND PROTEIN TO A SET OF CELL-TYPE-SPECIFIC GENES [J].
BENDER, A ;
SPRAGUE, GF .
CELL, 1987, 50 (05) :681-691
[5]   CHARACTERIZATION OF THE YEAST ARG5,6 GENE - DETERMINATION OF THE NUCLEOTIDE-SEQUENCE, ANALYSIS OF THE CONTROL REGION AND OF ARG5,6 TRANSCRIPT [J].
BOONCHIRD, C ;
MESSENGUY, F ;
DUBOIS, E .
MOLECULAR & GENERAL GENETICS, 1991, 226 (1-2) :154-166
[6]   Evolution of a New Function by Degenerative Mutation in Cephalochordate Steroid Receptors [J].
Bridgham, Jamie T. ;
Brown, Justine E. ;
Rodriguez-Mari, Adriana ;
Catchen, Julian M. ;
Thornton, Joseph W. .
PLOS GENETICS, 2008, 4 (09)
[7]   Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication [J].
Dennis, Megan Y. ;
Nuttle, Xander ;
Sudmant, Peter H. ;
Antonacci, Francesca ;
Graves, Tina A. ;
Nefedov, Mikhail ;
Rosenfeld, Jill A. ;
Sajjadian, Saba ;
Malig, Maika ;
Kotkiewicz, Holland ;
Curry, Cynthia J. ;
Shafer, Susan ;
Shaffer, Lisa G. ;
de Jong, Pieter J. ;
Wilson, Richard K. ;
Eichler, Evan E. .
CELL, 2012, 149 (04) :912-922
[8]   Evolution of increased complexity in a molecular machine [J].
Finnigan, Gregory C. ;
Hanson-Smith, Victor ;
Stevens, Tom H. ;
Thornton, Joseph W. .
NATURE, 2012, 481 (7381) :360-U143
[9]  
Force A, 1999, GENETICS, V151, P1531
[10]   Analyzing protein structure and function using ancestral gene reconstruction [J].
Harms, Michael J. ;
Thornton, Joseph W. .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2010, 20 (03) :360-366