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核仁组装与解体的细胞和分子生物学

Cell and molecular biology of nucleolar assembly and disassembly.

作者信息

Dimario Patrick J

机构信息

Department of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana 70803-1715, USA.

出版信息

Int Rev Cytol. 2004;239:99-178. doi: 10.1016/S0074-7696(04)39003-0.

Abstract

Nucleoli disassemble in prophase of the metazoan mitotic cycle, and they begin their reassembly (nucleologenesis) in late anaphase?early telophase. Nucleolar disassembly and reassembly were obvious to the early cytologists of the eighteenth and nineteenth centuries, and although this has lead to a plethora of literature describing these events, our understanding of the molecular mechanisms regulating nucleolar assembly and disassembly has expanded immensely just within the last 10-15 years. We briefly survey the findings of nineteenth-century cytologists on nucleolar assembly and disassembly, followed by the work of Heitz and McClintock on nucleolar organizers. A primer review of nucleolar structure and functions precedes detailed descriptions of modern molecular and microscopic studies of nucleolar assembly and disassembly. Nucleologenesis is concurrent with the reinitiation of rDNA transcription in telophase. The perichromosomal sheath, prenucleolar bodies, and nucleolar-derived foci serve as repositories for nucleolar processing components used in the previous interphase. Disassembly of the perichromosomal sheath along with the dynamic movements and compositional changes of the prenucleolar bodies and nucleolus-derived foci coincide with reactivation of rDNA synthesis within the chromosomal nucleolar organizers during telophase. Nucleologenesis is considered in various model organisms to provide breadth to our understanding. Nucleolar disassembly occurs at the onset of mitosis primarily as a result of the mitosis-specific phosphorylation of Pol I transcription factors and processing components. Although we have learned much regarding nucleolar assembly and disassembly, many questions still remain, and these questions are as vibrant for us today as early questions were for nineteenth- and early twentieth-century cytologists.

摘要

在后生动物有丝分裂周期的前期,核仁会解体,并在后期晚期至末期早期开始重新组装(核仁形成)。核仁的解体和重新组装在18和19世纪的早期细胞学家眼中是显而易见的,尽管这引发了大量描述这些事件的文献,但我们对调节核仁组装和解体的分子机制的理解仅在过去10 - 15年里有了极大的扩展。我们简要回顾了19世纪细胞学家关于核仁组装和解体的发现,接着介绍了海茨(Heitz)和麦克林托克(McClintock)关于核仁组织区的研究工作。在详细描述核仁组装和解体的现代分子及显微镜研究之前,先对核仁的结构和功能进行了初步综述。核仁形成与末期rDNA转录的重新启动同时发生。染色体周鞘、前核仁体和核仁衍生灶作为前一间期核仁加工成分的储存库。染色体周鞘的解体以及前核仁体和核仁衍生灶的动态运动和成分变化与末期染色体核仁组织区内rDNA合成的重新激活相吻合。我们考虑了各种模式生物中的核仁形成,以拓宽我们的理解。核仁解体主要发生在有丝分裂开始时,这主要是由于Pol I转录因子和加工成分的有丝分裂特异性磷酸化。尽管我们已经对核仁组装和解体了解了很多,但许多问题仍然存在,这些问题对我们今天来说仍然充满活力,就像早期问题对19世纪和20世纪初的细胞学家一样。

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