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具有条件性Lbh无效等位基因的小鼠的产生。

Generation of mice with a conditional Lbh null allele.

作者信息

Lindley Linsey E, Briegel Karoline J

机构信息

Department of Biochemistry and Molecular Biology, Braman Family Breast Cancer Institute at the Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, USA.

出版信息

Genesis. 2013 Jul;51(7):491-7. doi: 10.1002/dvg.22390. Epub 2013 May 3.

DOI:10.1002/dvg.22390
PMID:23495064
Abstract

Limb bud and heart (LBH) is a developmentally expressed, tissue-specific transcription cofactor in vertebrates that acts in the WNT signaling pathway, a genetic program critical for embryogenesis and adult tissue homeostasis. Aberrant gain-of-function of LBH is implicated in both human congenital disease and cancer. The normal physiological function of LBH has remained elusive owing to a lack of genetic loss-of-function models. Here, we have generated mice with a conditional null allele of Lbh by flanking exon 2 with loxP sites (Lbh(flox)). Homozygous Lbh(flox) and Lbh(loxP) mice, in which the Neo cassette was removed through FLPe-mediated recombination, were viable and fertile, indicating that these conditional Lbh alleles are fully functional. Lbh(loxP) mice were then crossed with a Rosa26-Cre line, resulting in ubiquitous deletion of exon 2 and abolishment of LBH protein expression. Mice homozygous for the Lbh null allele (Lbh(Δ)(2)) displayed normal embryonic development and postnatal growth with morphologies indistinguishable from wild-type littermates. However, mammary gland development, which occurs primarily after birth, was perturbed. Thus, the conditional Lbh allele will be a valuable tool to uncover the currently unknown tissue-specific roles of LBH in postnatal development and disease.

摘要

肢体芽与心脏(LBH)是脊椎动物中一种在发育过程中表达的组织特异性转录辅因子,它在WNT信号通路中发挥作用,WNT信号通路是对胚胎发生和成年组织内稳态至关重要的一个基因程序。LBH功能的异常获得与人类先天性疾病和癌症都有关联。由于缺乏基因功能缺失模型,LBH的正常生理功能一直难以捉摸。在此,我们通过在第2外显子两侧侧翼引入loxP位点(Lbh(flox)),生成了具有Lbh条件性无效等位基因的小鼠。通过FLPe介导的重组去除了Neo盒的纯合Lbh(flox)和Lbh(loxP)小鼠是有活力且可育的,这表明这些条件性Lbh等位基因具有完全功能。然后将Lbh(loxP)小鼠与Rosa26-Cre品系杂交,导致第2外显子普遍缺失且LBH蛋白表达缺失。Lbh无效等位基因纯合的小鼠(Lbh(Δ)(2))表现出正常的胚胎发育和出生后生长,其形态与野生型同窝仔无明显差异。然而,主要在出生后发生的乳腺发育受到了干扰。因此,条件性Lbh等位基因将成为揭示LBH在出生后发育和疾病中目前未知的组织特异性作用的一个有价值的工具。

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