Mattern K A, van der Kraan I, Schul W, de Jong L, van Driel R
BioCentrum Amsterdam, University of Amsterdam, Amsterdam, The Netherlands.
Exp Cell Res. 1999 Feb 1;246(2):461-70. doi: 10.1006/excr.1998.4267.
RNA polymerase II transcripts are complexed with heterogeneous nuclear ribonucleoprotein (hnRNP) proteins. These proteins are involved in several aspects of the maturation and transport of hnRNA. We performed a detailed study of the spatial distribution of four hnRNP proteins (hnRNP C, I, L, and U) in HeLa nuclei, using immunofluorescent labeling and confocal microscopy. Despite the fact that hnRNP proteins have been shown to coimmunoprecipitate, a hallmark of hnRNP proteins, we find that hnRNP C, I, and L have a spatial nuclear distribution that is not related to that of hnRNP U. We also examined the distribution of hnRNP proteins in relation to that of nascent transcripts. The four hnRNP proteins that we examined are not enriched at sites of RNA synthesis. Using antibodies against the nuclear poly(A)-binding protein (PAB II) we investigated the relationship between the distribution of hnRNP proteins and that of nuclear domains (nuclear speckles) that are enriched in splicing factors, poly(A)+RNA, and PAB II. We found that the four hnRNP proteins are not enriched in these domains. This indicates that the poly(A)+RNA, present in high concentration in speckles, is not complexed with these hnRNP proteins. This is in agreement with the notion that poly(A)+RNA in speckles is different from ordinary hnRNA. Previously, we have shown that hnRNP proteins are the major protein components of the fibrogranular internal nuclear matrix (K. A. Mattern et al. (1996) J. Cell. Biochem. 62, 275-289; K. A. Mattern et al. (1997) J. Cell. Biochem. 65, 42-52). We observed that in nuclear matrices the spatial distributions of the four hnRNP proteins, like that of nascent RNA and PAB II, are essentially the same as observed in intact nuclei. Moreover, also in nuclear matrix preparations, like in intact nuclei, nascent RNA and PAB II have spatial distributions that differ from those of hnRNP proteins. Our results are compatible with the notion that hnRNP proteins are able to form complexes of many different, probably overlapping, compositions.
RNA聚合酶II转录本与不均一核核糖核蛋白(hnRNP)结合。这些蛋白质参与hnRNA成熟和运输的多个方面。我们利用免疫荧光标记和共聚焦显微镜对HeLa细胞核中四种hnRNP蛋白(hnRNP C、I、L和U)的空间分布进行了详细研究。尽管hnRNP蛋白已被证明可进行共免疫沉淀,这是hnRNP蛋白的一个标志,但我们发现hnRNP C、I和L的核内空间分布与hnRNP U无关。我们还研究了hnRNP蛋白相对于新生转录本的分布情况。我们检测的这四种hnRNP蛋白在RNA合成位点并不富集。我们使用针对核聚腺苷酸结合蛋白(PAB II)的抗体,研究了hnRNP蛋白分布与富含剪接因子、聚腺苷酸+RNA和PAB II的核结构域(核斑点)分布之间的关系。我们发现这四种hnRNP蛋白在这些结构域中并不富集。这表明斑点中高浓度存在的聚腺苷酸+RNA并未与这些hnRNP蛋白结合。这与斑点中的聚腺苷酸+RNA不同于普通hnRNA的观点一致。此前,我们已经表明hnRNP蛋白是纤维颗粒状核内基质的主要蛋白质成分(K. A. Mattern等人,《细胞生物化学杂志》,1996年,第62卷,第275 - 289页;K. A. Mattern等人,《细胞生物化学杂志》,1997年,第65卷,第42 - 52页)。我们观察到,在核基质中,这四种hnRNP蛋白的空间分布,与新生RNA和PAB II的分布一样,与在完整细胞核中观察到的基本相同。此外,同样在核基质制备物中,如同在完整细胞核中一样,新生RNA和PAB II的空间分布与hnRNP蛋白不同。我们的结果与hnRNP蛋白能够形成许多不同的、可能相互重叠的组成的复合物这一观点相符。