Site-specific selfish genes as tools for the control and genetic engineering of natural populations

被引:437
作者
Burt, A
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Biol Sci, Ascot SL5 7PY, Berks, England
[2] Univ London Imperial Coll Sci Technol & Med, Ctr Populat Biol, Ascot SL5 7PY, Berks, England
关键词
population eradication; population genetic engineering; homing endonuclease genes; vector-borne diseases;
D O I
10.1098/rspb.2002.2319
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Site-specific selfish genes exploit host functions to copy themselves into a defined target DNA sequence, and include homing endonuclease genes, group II introns and some LINE-like transposable elements. If such genes can be engineered to target new host sequences, then they can be used to manipulate natural populations, even if the number of individuals released is a small fraction of the entire population. For example, a genetic load sufficient to eradicate a population can be imposed in fewer than 20 generations, if the target is an essential host gene, the knockout is recessive and the selfish gene has an appropriate promoter. There will be selection for resistance, but several strategies are available for reducing the likelihood of it evolving. These genes may also be used to genetically engineer natural populations, by means of population-wide gene knockouts, gene replacements and genetic transformations. By targeting sex-linked loci just prior to meiosis one may skew the population sex ratio, and by changing the promoter one may limit the spread of the gene to neighbouring populations. The proposed constructs are evolutionarily stable in the face of the mutations most likely to arise during their spread, and strategies are also available for reversing the manipulations.
引用
收藏
页码:921 / 928
页数:8
相关论文
共 43 条
  • [31] Targeted mutagenesis by homologous recombination in D-melanogaster
    Rong, YKS
    Titen, SW
    Xie, HB
    Golic, MM
    Bastiani, M
    Bandyopadhyay, P
    Olivera, BM
    Brodsky, M
    Rubin, GM
    Golic, KG
    [J]. GENES & DEVELOPMENT, 2002, 16 (12) : 1568 - 1581
  • [32] Gene targeting by homologous recombination in Drosophila
    Rong, YS
    Golic, KG
    [J]. SCIENCE, 2000, 288 (5473) : 2013 - 2018
  • [33] Directed evolution of the site specificity of Cre recombinase
    Santoro, SW
    Schultz, PG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (07) : 4185 - 4190
  • [34] Toward controlling gene expression at will:: Selection and design of zinc finger domains recognizing each of the 5′-GNN-3′ DNA target sequences
    Segal, DJ
    Dreier, B
    Beerli, RR
    Barbas, CF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) : 2758 - 2763
  • [35] Mutations altering the cleavage specificity of a homing endonuclease
    Seligman, LM
    Chevalier, BS
    Chadsey, MS
    Edwards, ST
    Savage, JH
    Veillet, AL
    [J]. NUCLEIC ACIDS RESEARCH, 2002, 30 (17) : 3870 - 3879
  • [36] SPIELMAN A, 2002, GENETICALLY ENG ORGA, P315
  • [37] SWEENY TL, 1978, GENETICS, V88, P427
  • [38] Transplantation of target site specificity by swapping the endonuclease domains of two LINEs
    Takahashi, H
    Fujiwara, H
    [J]. EMBO JOURNAL, 2002, 21 (03) : 408 - 417
  • [39] Insect population control using a dominant, repressible, lethal genetic system
    Thomas, DD
    Donnelly, CA
    Wood, RJ
    Alphey, LS
    [J]. SCIENCE, 2000, 287 (5462) : 2474 - 2476
  • [40] Microbe-induced cytoplasmic incompatibility as a mechanism for introducing transgenes into arthropod populations
    Turelli, M
    Hoffmann, AA
    [J]. INSECT MOLECULAR BIOLOGY, 1999, 8 (02) : 243 - 255