Lorković Zdravko J, Barta Andrea
Department of Medical Biochemistry, Max F Perutz Laboratories, Medical University of Vienna, Vienna, Austria.
PLoS One. 2008;3(12):e3989. doi: 10.1371/journal.pone.0003989. Epub 2008 Dec 22.
The biogenesis of spliceosomal snRNPs takes place in both the cytoplasm where Sm core proteins are added and snRNAs are modified at the 5' and 3' termini and in the nucleus where snRNP-specific proteins associate. U1 snRNP consists of U1 snRNA, seven Sm proteins and three snRNP-specific proteins, U1-70K, U1A, and U1C. It has been shown previously that after import to the nucleus U2 and U4/U6 snRNP-specific proteins first appear in Cajal bodies (CB) and then in splicing speckles. In addition, in cells grown under normal conditions U2, U4, U5, and U6 snRNAs/snRNPs are abundant in CBs. Therefore, it has been proposed that the final assembly of these spliceosomal snRNPs takes place in this nuclear compartment. In contrast, U1 snRNA in both animal and plant cells has rarely been found in this nuclear compartment.
METHODOLOGY/PRINCIPAL FINDINGS: Here, we analysed the subnuclear distribution of Arabidopsis U1 snRNP-specific proteins fused to GFP or mRFP in transiently transformed Arabidopsis protoplasts. Irrespective of the tag used, U1-70K was exclusively found in the nucleus, whereas U1A and U1C were equally distributed between the nucleus and the cytoplasm. In the nucleus all three proteins localised to CBs and nucleoli although to different extent. Interestingly, we also found that the appearance of the three proteins in nuclear speckles differ significantly. U1-70K was mostly found in speckles whereas U1A and U1C in approximately 90% of cells showed diffuse nucleoplasmic in combination with CBs and nucleolar localisation.
CONCLUSIONS/SIGNIFICANCE: Our data indicate that CBs and nucleolus are involved in the maturation of U1 snRNP. Differences in nuclear accumulation and distribution between U1-70K and U1A and U1C proteins may indicate that either U1-70K or U1A and U1C associate with, or is/are involved, in other nuclear processes apart from pre-mRNA splicing.
剪接体小核核糖核蛋白(snRNP)的生物合成发生在两个部位,一是细胞质,在那里添加Sm核心蛋白并对snRNA的5'和3'末端进行修饰;二是细胞核,在那里snRNP特异性蛋白发生结合。U1 snRNP由U1 snRNA、七种Sm蛋白以及三种snRNP特异性蛋白U1-70K、U1A和U1C组成。先前的研究表明,U2和U4/U6 snRNP特异性蛋白导入细胞核后,首先出现在卡哈尔体(CB)中,然后出现在剪接斑点中。此外,在正常条件下生长的细胞中,U2、U4、U5和U6 snRNAs/snRNPs在CB中含量丰富。因此,有人提出这些剪接体snRNP的最终组装发生在这个核区室中。相比之下,在动物和植物细胞中,很少在这个核区室中发现U1 snRNA。
方法/主要发现:在这里,我们分析了在瞬时转化的拟南芥原生质体中与绿色荧光蛋白(GFP)或单体红色荧光蛋白(mRFP)融合的拟南芥U1 snRNP特异性蛋白的亚核分布。无论使用何种标签,U1-70K仅在细胞核中被发现,而U1A和U1C在细胞核和细胞质中均匀分布。在细胞核中,这三种蛋白都定位于CB和核仁,尽管程度不同。有趣的是,我们还发现这三种蛋白在核斑点中的出现情况有显著差异。U1-70K大多存在于斑点中,而在大约90%的细胞中,U1A和U1C表现为弥漫性核质分布,并伴有CB和核仁定位。
结论/意义:我们的数据表明,CB和核仁参与了U1 snRNP的成熟过程。U1-70K与U1A和U1C蛋白在核积累和分布上的差异可能表明,U1-70K或U1A和U1C除了参与前体mRNA剪接外,还与其他核过程相关或参与其中。