Wansink D G, Schul W, van der Kraan I, van Steensel B, van Driel R, de Jong L
E.C. Slater Institute, University of Amsterdam, The Netherlands.
J Cell Biol. 1993 Jul;122(2):283-93. doi: 10.1083/jcb.122.2.283.
Several nuclear activities and components are concentrated in discrete nuclear compartments. To understand the functional significance of nuclear compartmentalization, knowledge on the spatial distribution of transcriptionally active chromatin is essential. We have examined the distribution of sites of transcription by RNA polymerase II (RPII) by labeling nascent RNA with 5-bromouridine 5'-triphosphate, in vitro and in vivo. Nascent RPII transcripts were found in over 100 defined areas, scattered throughout the nucleoplasm. No preferential localization was observed in either the nuclear interior or the periphery. Each transcription site may represent the activity of a single gene or, considering the number of active pre-mRNA genes in a cell, of a cluster of active genes. The relation between the distribution of nascent RPII transcripts and that of the essential splicing factor SC-35 was investigated in double labeling experiments. Antibodies against SC-35 recognize a number of well-defined, intensely labeled nuclear domains, in addition to labeling of more diffuse areas between these domains (Spector, D. L., X. -D. Fu, and T. Maniatis. 1991. EMBO (Eur. Mol. Biol. Organ.) J. 10:3467-3481). We observe no correlation between intensely labeled SC-35 domains and sites of pre-mRNA synthesis. However, many sites of RPII synthesis colocalize with weakly stained areas. This implies that contranscriptional splicing takes place in these weakly stained areas. These areas may also be sites where splicing is completed posttranscriptionally. Intensely labeled SC-35 domains may function as sites for assembly, storage, or regeneration of splicing components, or as compartments for degradation of introns.
几种核活动和组分集中在离散的核区室中。为了理解核区室化的功能意义,了解转录活性染色质的空间分布至关重要。我们通过在体外和体内用5-溴尿苷5'-三磷酸标记新生RNA,研究了RNA聚合酶II(RPII)转录位点的分布。在超过100个明确的区域中发现了新生的RPII转录本,这些区域散布在整个核质中。在核内部或周边均未观察到优先定位。每个转录位点可能代表单个基因的活性,或者考虑到细胞中活跃的前体mRNA基因的数量,代表一组活跃基因的活性。在双重标记实验中研究了新生RPII转录本的分布与必需剪接因子SC-35的分布之间的关系。除了标记这些结构域之间更弥散的区域外,针对SC-35的抗体还识别许多明确的、强烈标记的核结构域(Spector, D. L., X. -D. Fu, and T. Maniatis. 1991. EMBO (Eur. Mol. Biol. Organ.) J. 10:3467-3481)。我们观察到强烈标记的SC-35结构域与前体mRNA合成位点之间没有相关性。然而,许多RPII合成位点与弱染色区域共定位。这意味着共转录剪接发生在这些弱染色区域。这些区域也可能是转录后剪接完成的位点。强烈标记的SC-35结构域可能作为剪接组分组装、储存或再生的位点,或作为内含子降解的区室。