Gall J G, Bellini M, Wu Z, Murphy C
Department of Embryology, Carnegie Institution, Baltimore, Maryland 21210, USA.
Mol Biol Cell. 1999 Dec;10(12):4385-402. doi: 10.1091/mbc.10.12.4385.
We have examined the distribution of RNA transcription and processing factors in the amphibian oocyte nucleus or germinal vesicle. RNA polymerase I (pol I), pol II, and pol III occur in the Cajal bodies (coiled bodies) along with various components required for transcription and processing of the three classes of nuclear transcripts: mRNA, rRNA, and pol III transcripts. Among these components are transcription factor IIF (TFIIF), TFIIS, splicing factors, the U7 small nuclear ribonucleoprotein particle, the stem-loop binding protein, SR proteins, cleavage and polyadenylation factors, small nucleolar RNAs, nucleolar proteins that are probably involved in pre-rRNA processing, and TFIIIA. Earlier studies and data presented here show that several of these components are first targeted to Cajal bodies when injected into the oocyte and only subsequently appear in the chromosomes or nucleoli, where transcription itself occurs. We suggest that pol I, pol II, and pol III transcription and processing components are preassembled in Cajal bodies before transport to the chromosomes and nucleoli. Most components of the pol II transcription and processing pathway that occur in Cajal bodies are also found in the many hundreds of B-snurposomes in the germinal vesicle. Electron microscopic images show that B-snurposomes consist primarily, if not exclusively, of 20- to 30-nm particles, which closely resemble the interchromatin granules described from sections of somatic nuclei. We suggest the name pol II transcriptosome for these particles to emphasize their content of factors involved in synthesis and processing of mRNA transcripts. We present a model in which pol I, pol II, and pol III transcriptosomes are assembled in the Cajal bodies before export to the nucleolus (pol I), to the B-snurposomes and eventually to the chromosomes (pol II), and directly to the chromosomes (pol III). The key feature of this model is the preassembly of the transcription and processing machinery into unitary particles. An analogy can be made between ribosomes and transcriptosomes, ribosomes being unitary particles involved in translation and transcriptosomes being unitary particles for transcription and processing of RNA.
我们研究了两栖类卵母细胞核或生发泡中RNA转录和加工因子的分布情况。RNA聚合酶I(pol I)、pol II和pol III存在于卡哈尔体(卷曲体)中,同时还有三类核转录本(mRNA、rRNA和pol III转录本)转录和加工所需的各种组分。这些组分包括转录因子IIF(TFIIF)、TFIIS、剪接因子、U7小核核糖核蛋白颗粒、茎环结合蛋白、SR蛋白、切割和聚腺苷酸化因子、小核仁RNA、可能参与前体rRNA加工的核仁蛋白以及TFIIIA。此前的研究以及本文提供的数据表明,这些组分中的几种在注入卵母细胞后首先靶向卡哈尔体,随后才出现在转录发生的染色体或核仁中。我们认为,pol I、pol II和pol III转录及加工组分在转运至染色体和核仁之前先在卡哈尔体中进行预组装。在生发泡中数百个B型小核核糖核蛋白体中也发现了卡哈尔体中存在的pol II转录和加工途径的大多数组分。电子显微镜图像显示,B型小核核糖核蛋白体主要(如果不是唯一的话)由20至30纳米的颗粒组成,这些颗粒与从体细胞核切片中描述的染色质间颗粒非常相似。我们为这些颗粒提出“pol II转录体小体”这一名称,以强调其包含参与mRNA转录本合成和加工的因子。我们提出了一个模型,其中pol I、pol II和pol III转录体小体在卡哈尔体中组装,然后分别输出到核仁(pol I)、B型小核核糖核蛋白体并最终到染色体(pol II),以及直接到染色体(pol III)。该模型的关键特征是转录和加工机制预组装成单一颗粒。核糖体和转录体小体之间可以进行类比,核糖体是参与翻译的单一颗粒,而转录体小体是用于RNA转录和加工的单一颗粒。