Allison L A, Romaniuk P J, Bakken A H
Department of Zoology, University of Washington, Seattle 98195.
Dev Biol. 1991 Mar;144(1):129-44. doi: 10.1016/0012-1606(91)90485-l.
We studied the pathway of 5S RNA during oogenesis in Xenopus laevis from its storage in the cytoplasm to accumulation in the nucleus, the sequence requirements for the 5S RNA to follow that pathway, and the 5S RNA-protein interactions that occur during the mobilization of stored 5S RNA for assembly into ribosomes. In situ hybridization to sections of oocytes indicates that 5S RNA first becomes associated with the amplified nucleoli during vitellogenesis when the nucleoli are activity synthesizing ribosomal RNA and assembling ribosomes. When labeled 5S RNA is microinjected into the cytoplasm of stage V oocytes, it migrates into the nucleus, whether microinjected naked or complexed with the protein TFIIIA as a 7S RNP storage particle. During vitellogenesis, a nonribosome bound pool of 5S RNA complexed with ribosomal protein L5 (5S RNPs) is formed, which is present throughout the remainder of oogenesis. Immunoprecipitation assays on homogenates of microinjected oocytes showed that labeled 5S RNA can become complexed either with L5 or with TFIIIA. Nucleotides 11 through 108 of the 5S RNA molecule provide the necessary sequence and conformational information required for the formation of immunologically detectable complexes with TFIIIA or L5 and for nuclear accumulation. Furthermore, labeled 5S RNA from microinjected 7S RNPs can subsequently become associated with L5. Such labeled 5S RNA is found in both 5S RNPs and 7S RNPs in the cytoplasm, but only in 5S RNPs in the nucleus of microinjected oocytes. These data suggest that during oogenesis a major pathway for incorporation of 5S RNA into nascent ribosomes involves the migration of 5S RNA from the nucleus to the cytoplasm for storage in an RNP complex with TFIIIA, exchange of that protein association for binding with ribosomal protein L5, and a return to the nucleus for incorporation into ribosomes as they are being assembled in the amplified nucleoli.
我们研究了非洲爪蟾卵子发生过程中5S RNA从细胞质储存到细胞核积累的途径、5S RNA遵循该途径所需的序列要求,以及在储存的5S RNA动员用于组装核糖体过程中发生的5S RNA - 蛋白质相互作用。对卵母细胞切片进行原位杂交表明,在卵黄发生期间,当核仁活跃地合成核糖体RNA并组装核糖体时,5S RNA首先与扩增的核仁相关联。当将标记的5S RNA显微注射到V期卵母细胞的细胞质中时,无论它是裸注射还是与作为7S RNP储存颗粒的蛋白质TFIIIA复合注射,它都会迁移到细胞核中。在卵黄发生期间,形成了与核糖体蛋白L5复合的5S RNA非核糖体结合池(5S RNPs),其在卵子发生的其余过程中均存在。对显微注射卵母细胞匀浆进行的免疫沉淀分析表明,标记的5S RNA可以与L5或TFIIIA形成复合物。5S RNA分子的第11至108个核苷酸提供了与TFIIIA或L5形成免疫可检测复合物以及核积累所需的必要序列和构象信息。此外,来自显微注射的7S RNPs的标记5S RNA随后可以与L5相关联。这种标记的5S RNA在细胞质中的5S RNPs和7S RNPs中均有发现,但仅在显微注射卵母细胞的细胞核中的5S RNPs中存在。这些数据表明,在卵子发生过程中,5S RNA掺入新生核糖体的主要途径涉及5S RNA从细胞核迁移到细胞质,以与TFIIIA形成RNP复合物进行储存,将该蛋白质结合交换为与核糖体蛋白L5结合,然后返回细胞核以在扩增的核仁中组装核糖体时掺入核糖体。