Evidence for co-evolution of gene order and recombination rate

被引:124
作者
Pál, C
Hurst, LD [1 ]
机构
[1] Univ Bath, Dept Biol & Biochem, Bath BA2 7AY, Somerset, England
[2] Eotvos Lorand Univ, Dept Plant Taxon & Ecol, H-1117 Budapest, Hungary
关键词
D O I
10.1038/ng1111
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
There is increasing evidence in eukaryotic genomes that gene order is not random, even allowing for tandem duplication. Notably, in numerous genomes(1-6), genes of similar expression tend to be clustered. Are there other reasons for clustering of functionally similar genes? If genes are linked to enable genetic, rather than physical clustering, then we also expect that clusters of certain genes might be associated with blocks of reduced recombination rates. Here we show that, in yeast, essential genes are highly clustered and this clustering is independent of clustering of co-expressed genes and of tandem duplications. Adjacent pairs of essential genes are preferentially conserved through evolution. Notably, we also find that clusters of essential genes are in regions of low recombination and that larger clusters have lower recombination rates. These results suggest that selection acts to modify both the fine-scale intragenomic variation in the recombination rate and the distribution of genes and provide evidence for co-evolution of gene order and recombination rate.
引用
收藏
页码:392 / 395
页数:4
相关论文
共 28 条
  • [1] Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
    Altschul, SF
    Madden, TL
    Schaffer, AA
    Zhang, JH
    Zhang, Z
    Miller, W
    Lipman, DJ
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (17) : 3389 - 3402
  • [2] Saccharomyces Genome Database provides tools to survey gene expression and functional analysis data
    Ball, CA
    Jin, H
    Sherlock, G
    Weng, S
    Matese, JC
    Andrada, R
    Binkley, G
    Dolinski, K
    Dwight, SS
    Harris, MA
    Issel-Tarver, L
    Schroeder, R
    Botstein, D
    Cherry, JM
    [J]. NUCLEIC ACIDS RESEARCH, 2001, 29 (01) : 80 - 81
  • [3] A global analysis of Caenorhabditis elegans operons
    Blumenthal, T
    Evans, D
    Link, CD
    Guffanti, A
    Lawson, D
    Thierry-Mieg, J
    Thierry-Mieg, D
    Chiu, WL
    Duke, K
    Kiraly, M
    Kim, SK
    [J]. NATURE, 2002, 417 (6891) : 851 - 854
  • [4] A computational analysis of whole-genome expression data reveals chromosomal domains of gene expression
    Cohen, BA
    Mitra, RD
    Hughes, JD
    Church, GM
    [J]. NATURE GENETICS, 2000, 26 (02) : 183 - 186
  • [5] COOPER DN, 1999, HUMAN GENE EVOLUTION
  • [6] YPD™, PombePD™ and WormPD™:: model organism volumes of the BioKnowledge™ Library, an integrated resource for protein information
    Costanzo, MC
    Crawford, ME
    Hirschman, JE
    Kranz, JE
    Olsen, P
    Robertson, LS
    Skrzypek, MS
    Braun, BR
    Hopkins, KL
    Kondu, P
    Lengieza, C
    Lew-Smith, JE
    Tillberg, M
    Garrels, JI
    [J]. NUCLEIC ACIDS RESEARCH, 2001, 29 (01) : 75 - 79
  • [7] COX EC, 1972, NATURE-NEW BIOL, V92, P133
  • [8] Dickinson JR., 1999, METABOLISM MOL PHYSL
  • [9] A proteomic view of the Plasmodium falciparum life cycle
    Florens, L
    Washburn, MP
    Raine, JD
    Anthony, RM
    Grainger, M
    Haynes, JD
    Moch, JK
    Muster, N
    Sacci, JB
    Tabb, DL
    Witney, AA
    Wolters, D
    Wu, YM
    Gardner, MJ
    Holder, AA
    Sinden, RE
    Yates, JR
    Carucci, DJ
    [J]. NATURE, 2002, 419 (6906) : 520 - 526
  • [10] Functional genomic analysis of C-elegans chromosome I by systematic RNA interference
    Fraser, AG
    Kamath, RS
    Zipperlen, P
    Martinez-Campos, M
    Sohrmann, M
    Ahringer, J
    [J]. NATURE, 2000, 408 (6810) : 325 - 330