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肾脏中Foxc2基因的条件性敲除:通过双选系统高效生成单外显子基因的条件性等位基因

Conditional knockout of Foxc2 gene in kidney: efficient generation of conditional alleles of single-exon gene by double-selection system.

作者信息

Motojima Masaru, Ogiwara Sanae, Matsusaka Taiji, Kim Sang Yong, Sagawa Nobuho, Abe Koichiro, Ohtsuka Masato

机构信息

Department of Clinical Pharmacology, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa, 259-1193, Japan.

Support Center for Medical Research and Education, Tokai University School of Medicine, Isehara, Kanagawa, 259-1193, Japan.

出版信息

Mamm Genome. 2016 Feb;27(1-2):62-9. doi: 10.1007/s00335-015-9610-y. Epub 2015 Nov 5.

Abstract

Foxc2 is a single-exon gene and a key regulator in development of multiple organs, including kidney. To avoid embryonic lethality of conventional Foxc2 knockout mice, we conditionally deleted Foxc2 in kidneys. Conditional targeting of a single-exon gene involves the large floxed gene segment spanning from promoter region to coding region to avoid functional disruption of the gene by the insertion of a loxP site. Therefore, in ES cell clones surviving a conventional single-selection, e.g., neomycin-resistant gene (neo) alone, homologous recombination between the long floxed segment and target genome results in a high incidence of having only one loxP site adjacent to the selection marker. To avoid this limitation, we employed a double-selection system. We generated a Foxc2 targeting construct in which a floxed segment contained 4.6 kb mouse genome and two different selection marker genes, zeocin-resistant gene and neo, that were placed adjacent to each loxP site. After double-selection by zeocin and neomycin, 72 surviving clones were screened that yielded three correctly targeted clones. After floxed Foxc2 mice were generated by tetraploid complementation, we removed the two selection marker genes by a simultaneous-single microinjection of expression vectors for Dre and Flp recombinases into in vitro-fertilized eggs. To delete Foxc2 in mouse kidneys, floxed Foxc2 mice were mated with Pax2-Cre mice. Newborn Pax2-Cre; Foxc2(loxP/loxP) mice showed kidney hypoplasia and glomerular cysts. These results indicate the feasibility of generating floxed Foxc2 mice by double-selection system and simultaneous removal of selection markers with a single microinjection.

摘要

Foxc2是一个单外显子基因,是包括肾脏在内的多个器官发育过程中的关键调节因子。为避免传统Foxc2基因敲除小鼠出现胚胎致死性,我们在肾脏中条件性删除了Foxc2。单外显子基因的条件性靶向涉及从启动子区域到编码区域的大片段floxed基因,以避免loxP位点插入导致基因功能破坏。因此,在仅通过常规单重选择(例如仅新霉素抗性基因(neo))存活的胚胎干细胞克隆中,长floxed片段与目标基因组之间的同源重组导致在选择标记附近仅存在一个loxP位点的发生率很高。为避免这一限制,我们采用了双重选择系统。我们构建了一个Foxc2靶向载体,其中floxed片段包含4.6 kb的小鼠基因组以及两个不同的选择标记基因,即博来霉素抗性基因和neo,它们位于每个loxP位点附近。经过博来霉素和新霉素双重选择后,筛选出72个存活克隆,其中产生了三个正确靶向的克隆。通过四倍体互补产生floxed Foxc2小鼠后,我们通过将Dre和Flp重组酶的表达载体同时单次显微注射到体外受精的卵中,去除了两个选择标记基因。为了在小鼠肾脏中删除Foxc2,将floxed Foxc2小鼠与Pax2-Cre小鼠交配。新生的Pax2-Cre; Foxc2(loxP/loxP)小鼠表现出肾脏发育不全和肾小球囊肿。这些结果表明通过双重选择系统产生floxed Foxc2小鼠并通过单次显微注射同时去除选择标记的可行性。

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