Smith Abigail J, Ling Yan, Morgan Garry T
Institute of Genetics, University of Nottingham, United Kingdom.
Mol Biol Cell. 2003 Mar;14(3):1255-67. doi: 10.1091/mbc.e02-09-0601.
We have examined the localization and targeting of the RNA polymerase II (pol II) transcription elongation factor TFIIS in amphibian oocyte nuclei by immunofluorescence. Using a novel antibody against Xenopus TFIIS the major sites of immunostaining were found to be Cajal bodies, nuclear organelles that also contain pol II. Small granular structures attached to lampbrush chromosomes were also specifically stained but the transcriptionally active loops were not. Similar localization patterns were found for the newly synthesized myc-tagged TFIIS produced after injection of synthetic transcripts into the cytoplasm. The basis of the rapid and preferential targeting of TFIIS to Cajal bodies was investigated by examining the effects of deletion and site-specific mutations. Multiple regions of TFIIS contributed to efficient targeting including the domain required for its binding to pol II. The localization of TFIIS in Cajal bodies, and in particular the apparent involvement of pol II binding in achieving it, offer further support for a model in which Cajal bodies function in the preassembly of the transcriptional machinery. Although our findings are therefore consistent with TFIIS playing a role in early events of the transcription cycle, they also suggest that this elongation factor is not generally required during transcription in oocytes.
我们通过免疫荧光法研究了两栖类卵母细胞核中RNA聚合酶II(pol II)转录延伸因子TFIIS的定位和靶向作用。使用一种针对非洲爪蟾TFIIS的新型抗体,发现免疫染色的主要位点是卡哈尔体,这是一种也含有pol II的核细胞器。附着在灯刷染色体上的小颗粒结构也被特异性染色,但转录活性环未被染色。在将合成转录本注射到细胞质后产生的新合成的带有myc标签的TFIIS中也发现了类似的定位模式。通过研究缺失和位点特异性突变的影响,探讨了TFIIS快速且优先靶向卡哈尔体的基础。TFIIS的多个区域有助于高效靶向,包括其与pol II结合所需的结构域。TFIIS在卡哈尔体中的定位,特别是pol II结合在实现这一定位中明显的作用,为卡哈尔体在转录机器预组装中发挥作用的模型提供了进一步支持。因此,尽管我们的研究结果与TFIIS在转录周期早期事件中发挥作用一致,但它们也表明这种延伸因子在卵母细胞转录过程中并非普遍必需。