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在微真核生物 牡蛎 中,通过同源重组实现高效的基因靶向和外源 DNA 的去除。

Efficient gene targeting and removal of foreign DNA by homologous recombination in the picoeukaryote Ostreococcus.

机构信息

Sorbonne Universités, UPMC Univ Paris 06, UMR 7621, Laboratoire d'Océanographie Microbienne, Observatoire Océanologique, F-66650, Banyuls/mer, France; CNRS, UMR 7621, Laboratoire d'Océanographie Microbienne, Observatoire Océanologique, F-66650, Banyuls/mer, France.

出版信息

Plant J. 2014 Jun;78(6):1073-83. doi: 10.1111/tpj.12530. Epub 2014 May 23.

Abstract

With fewer than 8000 genes and a minimalist cellular organization, the green picoalga Ostreococcus tauri is one of the simplest photosynthetic eukaryotes. Ostreococcus tauri contains many plant-specific genes but exhibits a very low gene redundancy. The haploid genome is extremely dense with few repeated sequences and rare transposons. Thanks to the implementation of genetic transformation and vectors for inducible overexpression/knockdown this picoeukaryotic alga has emerged in recent years as a model organism for functional genomics analyses and systems biology. Here we report the development of an efficient gene targeting technique which we use to knock out the nitrate reductase and ferritin genes and to knock in a luciferase reporter in frame to the ferritin native protein. Furthermore, we show that the frequency of insertion by homologous recombination is greatly enhanced when the transgene is designed to replace an existing genomic insertion. We propose that a natural mechanism based on homologous recombination may operate to remove inserted DNA sequences from the genome.

摘要

小球藻是最简单的光合真核生物之一,其基因组大约有 8000 个基因,细胞结构非常简单。小球藻含有许多植物特异性基因,但基因冗余度很低。其单倍体基因组非常密集,重复序列和转座子很少。由于遗传转化的实施以及诱导过表达/敲低载体的构建,这种微型真核藻类近年来已成为功能基因组学分析和系统生物学的模式生物。在这里,我们报告了一种高效的基因靶向技术的开发,我们利用该技术敲除硝酸盐还原酶和铁蛋白基因,并将荧光素酶报告基因整合到铁蛋白天然蛋白中。此外,我们还发现当转基因设计用于替换现有基因组插入时,同源重组的插入频率大大提高。我们提出,一种基于同源重组的自然机制可能用于从基因组中去除插入的 DNA 序列。

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