...
首页> 外文期刊>Parasitology >Transgenesis in Strongyloides and related parasitic nematodes: historical perspectives, current functional genomic applications and progress towards gene disruption and editing
【24h】

Transgenesis in Strongyloides and related parasitic nematodes: historical perspectives, current functional genomic applications and progress towards gene disruption and editing

机译:酮酮和相关寄生线虫的转基因:历史观点,目前的功能基因组应用以及对基因破坏和编辑的进展

获取原文
获取原文并翻译 | 示例
           

摘要

Transgenesis for Strongyloides and Parastrongyloides was accomplished in 2006 and is based on techniques derived for Caenorhabditis elegans over two decades earlier. Adaptation of these techniques has been possible because Strongyloides and related parasite genera carry out at least one generation of free-living development, with adult males and females residing in soil contaminated by feces from an infected host. Transgenesis in this group of parasites is accomplished by microinjecting DNA constructs into the syncytia of the distal gonads of free-living females. In Strongyloides stercoralis, plasmid-encoded transgenes are expressed in promoter-regulated fashion in the F1 generation following gene transfer but are silenced subsequently. Stable inheritance and expression of transgenes in S. stercoralis requires their integration into the genome, and stable lines have been derived from integrants created using the piggyBac transposon system. More direct investigations of gene function involving expression of mutant transgene constructs designed to alter intracellular trafficking and developmental regulation have shed light on the function of the insulin-regulated transcription factor Ss-DAF-16. Transgenesis in Strongyloides and Parastrongyloides opens the possibility of powerful new methods for genome editing and transcriptional manipulation in this group of parasites. Proof of principle for one of these, CRISPR/Cas9, is presented in this review.
机译:2006年完成酮酮和Parastonylyes的转基因,基于早些时多十年来,基于在二十年内为Caenorhabdisizys的技术。这些技术的改编是可能的,因为酮和相关寄生虫属于至少一代自由生植物发育,成年男性和居住在受感染的宿主受粪便污染的土壤中的女性。该组寄生虫中的转基因通过微观的DNA构建体来完成将DNA构建体分成自由生物雌性的远端性腺的合胞菌。在酮化物中,在基因转移后的F1代,在F1生成中以启动子调节的方式表达质粒编码的转基因,但随后沉默。稳定的遗传和转基因在S. Stercoralis中的表达需要它们的整合到基因组中,并且稳定的线条来自使用Piggybac转座系统产生的整合体。更直接地研究涉及设计用于改变细胞内运输和发育调节的突变转基因构建体的表达的基因功能对胰岛素调节转录因子SS-DAF-16的功能具有脱光。抗酮和帕拉氏蛋白中的转基因对该组寄生虫中的基因组编辑和转录操作的强大新方法的可能性开辟了强大的新方法。在本次审查中介绍了其中一个CRISPR / CAS9原则证明。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号