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四环素转录激活子转基因小鼠造血系统中可诱导表达的变异性。

Variability of inducible expression across the hematopoietic system of tetracycline transactivator transgenic mice.

机构信息

Molecular Medicine Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.

出版信息

PLoS One. 2013;8(1):e54009. doi: 10.1371/journal.pone.0054009. Epub 2013 Jan 11.

Abstract

The tetracycline (tet)-regulated expression system allows for the inducible overexpression of protein-coding genes, or inducible gene knockdown based on expression of short hairpin RNAs (shRNAs). The system is widely used in mice, however it requires robust expression of a tet transactivator protein (tTA or rtTA) in the cell type of interest. Here we used an in vivo tet-regulated fluorescent reporter approach to characterise inducible gene/shRNA expression across a range of hematopoietic cell types of several commonly used transgenic tet transactivator mouse strains. We find that even in strains where the tet transactivator is expressed from a nominally ubiquitous promoter, the efficiency of tet-regulated expression can be highly variable between hematopoietic lineages and between differentiation stages within a lineage. In some cases tet-regulated reporter expression differs markedly between cells within a discrete, immunophenotypically defined population, suggesting mosaic transactivator expression. A recently developed CAG-rtTA3 transgenic mouse displays intense and efficient reporter expression in most blood cell types, establishing this strain as a highly effective tool for probing hematopoietic development and disease. These findings have important implications for interpreting tet-regulated hematopoietic phenotypes in mice, and identify mouse strains that provide optimal tet-regulated expression in particular hematopoietic progenitor cell types and mature blood lineages.

摘要

四环素(tet)调控表达系统允许诱导过表达编码蛋白的基因,或基于短发夹 RNA(shRNA)表达诱导基因敲低。该系统在小鼠中广泛使用,但它需要在感兴趣的细胞类型中强有力地表达 tet 转录激活蛋白(tTA 或 rtTA)。在这里,我们使用体内 tet 调控的荧光报告基因方法,对几种常用的 tet 转录激活剂转基因小鼠品系的一系列造血细胞类型中的诱导基因/shRNA 表达进行了特征描述。我们发现,即使 tet 转录激活剂是由名义上普遍的启动子表达的,tet 调控的表达效率在造血谱系之间和谱系内的分化阶段之间也可能有很大的差异。在某些情况下,tet 调控的报告基因表达在离散的、免疫表型定义的细胞群内有明显差异,提示存在嵌合转录激活剂表达。最近开发的 CAG-rtTA3 转基因小鼠在大多数血细胞类型中显示出强烈和高效的报告基因表达,使该品系成为研究造血发育和疾病的有效工具。这些发现对解释小鼠中 tet 调控的造血表型具有重要意义,并确定了在特定造血祖细胞类型和成熟血液谱系中提供最佳 tet 调控表达的小鼠品系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2df/3543435/a8ece4acc621/pone.0054009.g001.jpg

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