von Waldthausen Dagmar C, Schneider Marlon R, Renner-Müller Ingrid, Rauleder Dirk N, Herbach Nadja, Aigner Bernhard, Wanke Rüdiger, Wolf Eckhard
Institute of Molecular Animal Breeding and Biotechnology and Laboratory for Functional Genome Analysis (LAFUGA), Gene Center, LMU Munich, Feodor-Lynen-Strasse 25, Munich, Germany.
Transgenic Res. 2008 Aug;17(4):479-88. doi: 10.1007/s11248-007-9163-2. Epub 2007 Dec 20.
Transgenic mice overexpressing growth hormone (GH) display a plethora of phenotypic alterations and provide unique models for studying and influencing consequences of chronic GH excess. Since the first report on GH transgenic mice was published in 1982, many different mouse models overexpressing GH from various species at different levels and with different tissue specificities were established, most of them on random-bred or hybrid genetic background. We have generated a new transgenic mouse model on FVB/N inbred background, expressing bovine (b) GH under the control of the chicken beta-actin promoter (cbetaa). cbetaa-bGH transgenic mice exhibit ubiquitous expression of bGH mRNA and protein and circulating bGH levels in the range of several microg/ml, resulting in markedly stimulated growth and the characteristic spectrum of pathological lesions which were described in previous GH overexpressing mouse models. Importantly, a consistent sequence of renal alterations is observed, mimicking progressive kidney disease in human patients. The novel, genetically standardized GH transgenic mouse model is ideal for holistic transcriptome and proteome studies aiming at the identification of the molecular mechanisms underlying GH-induced pathological alterations especially in the kidney. Moreover, genetically defined cbetaa-bGH mice facilitate random mutagenesis screens for modifier genes which influence the effects of chronic GH excess and associated pathological lesions.
过度表达生长激素(GH)的转基因小鼠表现出大量的表型改变,为研究和影响慢性GH过量的后果提供了独特的模型。自1982年首次报道GH转基因小鼠以来,已经建立了许多不同的小鼠模型,这些模型在不同水平和具有不同组织特异性的情况下过度表达来自各种物种的GH,其中大多数是在随机繁殖或杂交遗传背景上建立的。我们在FVB/N近交背景上生成了一种新的转基因小鼠模型,该模型在鸡β-肌动蛋白启动子(cbetaa)的控制下表达牛(b)GH。cbetaa-bGH转基因小鼠表现出bGH mRNA和蛋白质的普遍表达,循环bGH水平在几微克/毫升范围内,导致生长明显受刺激,并出现先前GH过度表达小鼠模型中描述的特征性病理病变谱。重要的是,观察到了一致的肾脏改变序列,类似于人类患者的进行性肾脏疾病。这种新的、基因标准化的GH转基因小鼠模型非常适合进行整体转录组和蛋白质组研究,旨在确定GH诱导的病理改变尤其是肾脏病理改变的分子机制。此外,基因定义的cbetaa-bGH小鼠便于对影响慢性GH过量及其相关病理病变的修饰基因进行随机诱变筛选。