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DESCRIPTION (provided by applicant): Vector-borne diseases such as malaria and dengue hemorrhagic fever remain large public health burdens, and novel interventions are still needed. The emerging field of genetics-based control has seen a number of recent laboratory successes with the generation of pathogen- resistant mosquito strains as well as female-killing strains. The development of genetically modified mosquitoes still largely relies upon classical transposable element transformation, although several recent reports have made use of the site-specific integrase C31. While site- specificity allows the investigator to examine multiple transgenes in the same genetic environment, an unfortunate consequence of the attP-attB C31 system is that as a result of recombination the entire bacterial plasmid becomes integrated into the mosquito genome. This is undesirable, as many of the currently developed transgenic mosquito strains are intended as specific genetic interventions to control a targeted vector-borne pathogen where such antibiotic resistance genes could be transferred to native bacterial species. We hypothesize that recombinase-mediated cassette exchange (RMCE) can be an efficient means of delivering transgenes into important disease vector species in a site-specific manner, without the negative consequences of co-integrating bacterial sequences. As such, we propose to (1) test a panel of heterospecific lox sites for their ability to resist intramolecular recombination i cis and promote RMCE in the embryos of the dengue vector Aedes aegypti and the malaria vector Anopheles gambiae; (2) generate transgenic docking strains based on the best candidate heterospecific lox sites and determine the rate of RMCE for each using the phage P1 cre recombinase. Such an alternative system which preserves the ability to perform site-specific recombination, but avoids the integration of bacterial sequences and remains as easy to use as TE-based helper plasmids would likely be much more widely adopted, and would help to drive the field of novel genetics- based control strategies for vector-borne diseases.
期刊论文(4)
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会议论文
DOI: 10.1007/s10577-014-9450-8
发表时间: 2015-03
期刊: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology
影响因子: --
作者: [Overcash JM, Aryan A, Myles KM, Adelman ZN]
通讯作者: Adelman ZN
DOI: 10.1371/journal.pone.0060082
发表时间: 2013
期刊: PloS one
影响因子: 3.7
作者: [Aryan A, Anderson MA, Myles KM, Adelman ZN]
通讯作者: Adelman ZN
Self-eliminating strategy to control gene drive
  • 批准号:
    10401434
  • 项目类别:
  • 资助金额:
    $74.11万
  • 财政年份:
    2020
  • 负责人:
    Zach N. Adelman
  • 依托单位:
Self-eliminating strategy to control gene drive
  • 批准号:
    10202464
  • 项目类别:
  • 资助金额:
    $74.19万
  • 财政年份:
    2020
  • 负责人:
    Zach N. Adelman
  • 依托单位:
The role of the circadian clock in the behavior of the malaria mosquito Anopheles coluzzii
  • 批准号:
    10083702
  • 项目类别:
  • 资助金额:
    $18.94万
  • 财政年份:
    2020
  • 负责人:
    Zach N. Adelman
  • 依托单位:
Self-eliminating strategy to control gene drive
  • 批准号:
    10625308
  • 项目类别:
  • 资助金额:
    $74.02万
  • 财政年份:
    2020
  • 负责人:
    Zach N. Adelman
  • 依托单位:
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