Schymeinsky Jürgen, Nedbal Sabine, Miosge Nicolai, Pöschl Ernst, Rao Cherie, Beier David R, Skarnes William C, Timpl Rupert, Bader Bernhard L
Department of Protein Chemistry, Max-Planck-Institute for Biochemistry, D-82152 Martinsried, Germany.
Mol Cell Biol. 2002 Oct;22(19):6820-30. doi: 10.1128/MCB.22.19.6820-6830.2002.
Nidogens are highly conserved proteins in vertebrates and invertebrates and are found in almost all basement membranes. According to the classical hypothesis of basement membrane organization, nidogens connect the laminin and collagen IV networks, so stabilizing the basement membrane, and integrate other proteins. In mammals two nidogen proteins, nidogen-1 and nidogen-2, have been discovered. Nidogen-2 is typically enriched in endothelial basement membranes, whereas nidogen-1 shows broader localization in most basement membranes. Surprisingly, analysis of nidogen-1 gene knockout mice presented evidence that nidogen-1 is not essential for basement membrane formation and may be compensated for by nidogen-2. In order to assess the structure and in vivo function of the nidogen-2 gene in mice, we cloned the gene and determined its structure and chromosomal location. Next we analyzed mice carrying an insertional mutation in the nidogen-2 gene that was generated by the secretory gene trap approach. Our molecular and biochemical characterization identified the mutation as a phenotypic null allele. Nidogen-2-deficient mice show no overt abnormalities and are fertile, and basement membranes appear normal by ultrastructural analysis and immunostaining. Nidogen-2 deficiency does not lead to hemorrhages in mice as one may have expected. Our results show that nidogen-2 is not essential for basement membrane formation or maintenance.
巢蛋白是脊椎动物和无脊椎动物中高度保守的蛋白质,几乎存在于所有基底膜中。根据基底膜组织的经典假说,巢蛋白连接层粘连蛋白和IV型胶原网络,从而稳定基底膜,并整合其他蛋白质。在哺乳动物中,已发现两种巢蛋白,即巢蛋白-1和巢蛋白-2。巢蛋白-2通常在内皮基底膜中富集,而巢蛋白-1在大多数基底膜中定位更广泛。令人惊讶的是,对巢蛋白-1基因敲除小鼠的分析表明,巢蛋白-1对基底膜形成并非必不可少,可能由巢蛋白-2代偿。为了评估小鼠中巢蛋白-2基因的结构和体内功能,我们克隆了该基因并确定了其结构和染色体定位。接下来,我们分析了携带通过分泌基因陷阱方法产生的巢蛋白-2基因插入突变的小鼠。我们的分子和生化特征鉴定该突变为表型无效等位基因。巢蛋白-2缺陷型小鼠没有明显异常且可育,通过超微结构分析和免疫染色,基底膜看起来正常。巢蛋白-2缺陷不会像人们预期的那样导致小鼠出血。我们的结果表明,巢蛋白-2对基底膜的形成或维持并非必不可少。