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Expanding the C. elegans toolbox into a toolshed

机译:将秀丽隐杆线虫工具箱扩展到工具箱

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Since Sydney Brenner's proposal to exploit Caenorhabditis elegans to unravel the genetic basis of metazoan development and the nervous system [1], technological developments have turned this model organism into one of the premier resources for studying multiple facets of cell biology. Several excellent compendia outline some of these methodological advancements [2-8]. In addition, the WormMetrjods section of WormBook (http://www.wormbook.org/ toc_wormmethods.html) provides a rich compilation of C. elegans methodology. The goal of this edition of Methods is to highlight recent innovations that have expanded the repertoire of techniques available to C. elegans investigators, and to update methods not covered extensively by these other references. The study of gene function by transgenesis is one of the most powerful technologies available to C elegans investigators. Recently, the application of genome editing has enhanced significantly the scope and precision of these methods. The first 8 articles of this edition of Methods provide added insight into these technologies. Waaijers and Boxem, discuss practical considerations in the use of the CR1SPR/Cas9 system to engineer the genome. They describe non-homologous end-joining or homologous recombination methods in combination with modified DNA templates [9].
机译:自从悉尼·布伦纳提出利用秀丽隐杆线虫揭示后生动物发育和神经系统的遗传基础[1]的提议以来,技术发展已使这种模式生物成为研究细胞生物学多个方面的主要资源之一。几个优秀的纲要概述了这些方法学的进步[2-8]。此外,WormBook的WormMetrjods部分(http://www.wormbook.org/ toc_wormmethods.html)提供了丰富的秀丽隐​​杆线虫方法学汇编。本版《方法》的目的是重点介绍扩大了秀丽隐杆线虫研究人员可用技术范围的最新创新,并更新这些参考文献未广泛涵盖的方法。通过转基因研究基因功能是秀丽线虫研究人员可获得的最强大的技术之一。最近,基因组编辑的应用大大增强了这些方法的范围和精度。本版《方法》的前8篇文章提供了对这些技术的更多了解。 Waaijers和Boxem讨论了使用CR1SPR / Cas9系统改造基因组的实际考虑。他们描述了结合修饰的DNA模板的非同源末端连接或同源重组方法[9]。

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