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在牛基因组中存在一个有利于转基因表达的phiC31整合酶介导的整合热点。

A phiC31 integrase-mediated integration hotspot in favor of transgene expression exists in the bovine genome.

作者信息

Ou Hai-Long, Huang Ying, Qu Li-Juan, Xu Miao, Yan Jing-Bin, Ren Zhao-Rui, Huang Shu-Zhen, Zeng Yi-Tao

机构信息

Shanghai Institute of Medical Genetics, Shanghai Jiao Tong University, China.

出版信息

FEBS J. 2009 Jan;276(1):155-63. doi: 10.1111/j.1742-4658.2008.06762.x.

Abstract

phiC31 integrase, a site-specific recombinase, can effectively mediate foreign genes bearing an attB sequence integrated into pseudo attP sites. We have previously identified two pseudo attP sites, BpsF1 and BpsM1 from the bovine genome. In this study, two new pseudo attP sites, BF4 and BF10, were discovered using half-nested inverse PCR from cow fibroblasts. The genomic locations of these two pseudo attP sites were identified by direct sequencing and a BLAST search, and it was confirmed that they reside at positions 4q31 and 10q35 by fluorescence in situ hybridization analysis. Subsequently, the distinct integration frequencies of the four pseudo attP sites were examined. The BF4 site was identified as a hotspot where site-specific integration occurred in most of the cell clones examined, accounting for 74% (42/57) of the integration; much more than the integration frequency for BF10 (7%; 4/57), BpsF1 (7%; 4/57) and BpsM1 (0/57). Interestingly, similar to other hotspots identified in the human and mouse genomes, in which transgenes integrated at hotspots result in high expression, the GFP gene integrated at hotspot BF4 was expressed at high levels in cow fibroblasts, as confirmed by fluorescence microscopy and FACS analysis. Furthermore, ELISA showed that the expression level of the GFP gene integrated at the BF4 site averaged approximately 328 microg x mg(-1), which is more than twofold higher than that integrated at the BF10 site. This study suggests that somatic cells carrying a desired gene integrated at the BF4 site can be used as nuclear donors to generate valuable transgenic animals by nuclear transfer.

摘要

φC31整合酶是一种位点特异性重组酶,能够有效地介导携带attB序列的外源基因整合到假attP位点。我们之前已从牛基因组中鉴定出两个假attP位点,即BpsF1和BpsM1。在本研究中,利用半巢式反向PCR从牛成纤维细胞中发现了两个新的假attP位点,BF4和BF10。通过直接测序和BLAST搜索确定了这两个假attP位点的基因组位置,并通过荧光原位杂交分析证实它们位于4q31和10q35位置。随后,检测了这四个假attP位点不同的整合频率。BF4位点被确定为一个热点,在所检测的大多数细胞克隆中发生了位点特异性整合,占整合的74%(42/57);远高于BF10(7%;4/57)、BpsF1(7%;4/57)和BpsM1(0/57)的整合频率。有趣的是,与在人类和小鼠基因组中鉴定出的其他热点相似,转基因在热点处整合会导致高表达,通过荧光显微镜和流式细胞仪分析证实,在热点BF4处整合的绿色荧光蛋白(GFP)基因在牛成纤维细胞中高表达。此外,酶联免疫吸附测定(ELISA)表明,在BF4位点整合的GFP基因的表达水平平均约为328μg·mg-1,比在BF10位点整合的表达水平高出两倍多。本研究表明,携带在BF4位点整合的所需基因的体细胞可作为核供体,通过核移植产生有价值的转基因动物。

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