Visa N, Puvion-Dutilleul F, Harper F, Bachellerie J P, Puvion E
Laboratoire de Biologie et Ultrastructure du Noyau, CNRS, UPR 272, Villejuif, France.
Exp Cell Res. 1993 Sep;208(1):19-34. doi: 10.1006/excr.1993.1218.
We used a biotinylated poly(dT) probe to localize poly(A) RNA in HeLa cells at optical and electron microscope levels. We established that the fluorescent speckled staining pattern corresponds at the ultrastructural level to the labeling of perichromatin fibrils, at least part of the population of perichromatin granules, and clusters of interchromatin granules. Coiled bodies and the interchromatin granule-associated zones, a recently described subcompartment containing U1 but not U2 snRNA, were not labeled. The density of the labeling of interchromatin granule clusters exceeded by three to five times that of the surrounding extranucleolar area. These results are discussed in relation to the role of perichromatin fibrils in splicing of pre-mRNA and to the possible involvement of interchromatin granules in the assembly of mature spliceosomes as well as in sorting and/or coordination of RNA molecules to be transported to the cytoplasm.
我们使用生物素化的聚(dT)探针在光学显微镜和电子显微镜水平上对HeLa细胞中的聚(A)RNA进行定位。我们确定,荧光斑点染色模式在超微结构水平上对应于染色质周边纤维、至少部分染色质周边颗粒群体以及染色质间颗粒簇的标记。卷曲小体和染色质间颗粒相关区域(最近描述的一个含有U1但不含U2 snRNA的亚区室)未被标记。染色质间颗粒簇的标记密度比周围核仁外区域高出三到五倍。结合染色质周边纤维在mRNA前体剪接中的作用以及染色质间颗粒在成熟剪接体组装中可能的参与情况,以及在RNA分子分选和/或协调转运至细胞质中的作用,对这些结果进行了讨论。