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黑腹果蝇中的转基因技术。

Transgenesis in Drosophila melanogaster.

作者信息

Ringrose Leonie

机构信息

IMBA - Institute of Molecular Biotechnology GmbH, Vienna, Austria.

出版信息

Methods Mol Biol. 2009;561:3-19. doi: 10.1007/978-1-60327-019-9_1.

Abstract

Transgenesis in Drosophila melanogaster relies upon direct microinjection of embryos and subsequent crossing of surviving adults. The necessity of crossing single flies to screen for transgenic events limits the range of useful transgenesis techniques to those that have a very high frequency of integration, so that about 1 in 10 to 1 in 100 surviving adult flies carry a transgene. Until recently, only random P-element transgenesis fulfilled these criteria. However, recent advances have brought homologous recombination and site-directed integration up to and beyond this level of efficiency. For all transgenesis techniques in Drosophila melanogaster, microinjection of embryos is the central procedure. This chapter gives a detailed protocol for microinjection, and aims to enable the reader to use it for both site-directed integration and for P-element transgenesis.

摘要

在黑腹果蝇中进行转基因操作依赖于对胚胎的直接显微注射以及随后对存活成虫的杂交。由于需要对单只果蝇进行杂交以筛选转基因事件,这就将有用的转基因技术范围限制在那些具有非常高整合频率的技术上,这样大约每10到100只存活的成年果蝇中就有1只携带转基因。直到最近,只有随机P因子转基因满足这些标准。然而,最近的进展已使同源重组和定点整合达到并超过了这种效率水平。对于黑腹果蝇的所有转基因技术而言,胚胎显微注射是核心步骤。本章给出了显微注射的详细方案,旨在使读者能够将其用于定点整合和P因子转基因操作。

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