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有证据表明,据报道为一种分化特异性桥粒蛋白的“pinin”实际上是一种广泛存在的核蛋白。

Evidence that "pinin", reportedly a differentiation-specific desmosomal protein, is actually a widespread nuclear protein.

作者信息

Brandner J M, Reidenbach S, Franke W W

机构信息

Division of Cell Biology, German Cancer Research Center, Heidelberg, Germany.

出版信息

Differentiation. 1997 Dec;62(3):119-27. doi: 10.1046/j.1432-0436.1997.6230119.x.

Abstract

A protein recently described as a desmosome-specific molecule involved in anchoring intermediate-sized filaments (IFs) to the desmosomal plaque, and hence named "pinin" [43], has been known in our laboratory for several years as a strictly nuclear protein occurring in a wide range of cell types, including many that are totally devoid of desmosomes. Using a series of specific antibodies we have localized the protein in the nucleoplasm of cultured cells, blood cells and solid tissues of diverse vertebrate species, from oocytes to erythrocytes of amphibia and from liver to connective tissue and fibroblasts in mammals. Desmosomes have consistently been negative, and the nuclear specificity of the immunolocalization reactions has also been directly demonstrated by double-label immunofluorescence microscopy. From our results we conclude that this nuclear protein, characterized by a domain exceptionally rich in serine residues and hence termed DRS-protein, occurs in at least two genetically different forms in a diffusible state as well as in special ribonucleoprotein-particles, "speckles" [6], and is a widespread if not ubiquitous nuclear protein. Consequently it must serve nuclear functions rather than "pinning" IFs to plasma membranes and does not provide a new reliable marker for desmosomes and epithelial or myocardial differentiation.

摘要

一种最近被描述为参与将中等大小的细丝(IFs)锚定到桥粒斑的桥粒特异性分子,并因此被命名为“桥粒蛋白”[43],在我们实验室中作为一种严格意义上的核蛋白已被知晓数年,它存在于多种细胞类型中,包括许多完全没有桥粒的细胞类型。我们使用一系列特异性抗体,已将该蛋白定位在不同脊椎动物物种的培养细胞、血细胞和实体组织的核质中,从两栖动物的卵母细胞到红细胞,以及从哺乳动物的肝脏到结缔组织和成纤维细胞。桥粒始终呈阴性,免疫定位反应的核特异性也通过双标记免疫荧光显微镜直接得到了证实。根据我们的结果,我们得出结论,这种以富含丝氨酸残基的结构域为特征并因此被称为DRS蛋白的核蛋白,以可扩散状态以及特殊的核糖核蛋白颗粒“斑点”[6]的形式至少以两种基因不同的形式存在,并且是一种广泛存在(即便不是普遍存在)的核蛋白。因此,它必定发挥核功能,而不是将IFs“固定”到质膜上,并且不能为桥粒以及上皮或心肌分化提供新的可靠标记。

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