RNA聚合酶Ⅲ
生物
RNA聚合酶Ⅱ
RNA聚合酶Ⅰ
核糖体生物发生
遗传学
抄写(语言学)
核糖体
核糖核酸
RNA聚合酶
细胞生物学
基因
基因表达
发起人
语言学
哲学
作者
Julia Macintosh,Julia Macintosh,Geneviève Bernard,Paul A. Trainor
标识
DOI:10.1016/j.semcdb.2022.03.027
摘要
Ribosomes are macromolecular machines that are globally required for the translation of all proteins in all cells. Ribosome biogenesis, which is essential for cell growth, proliferation and survival, commences with transcription of a variety of RNAs by RNA Polymerases I and III. RNA Polymerase I (Pol I) transcribes ribosomal RNA (rRNA), while RNA Polymerase III (Pol III) transcribes 5S ribosomal RNA and transfer RNAs (tRNA) in addition to a wide variety of small non-coding RNAs. Interestingly, despite their global importance, disruptions in Pol I and Pol III function result in tissue-specific developmental disorders, with craniofacial anomalies and leukodystrophy/neurodegenerative disease being among the most prevalent. Furthermore, pathogenic variants in genes encoding subunits shared between Pol I and Pol III give rise to distinct syndromes depending on whether Pol I or Pol III function is disrupted. In this review, we discuss the global roles of Pol I and III transcription, the consequences of disruptions in Pol I and III transcription, disorders arising from pathogenic variants in Pol I and Pol III subunits, and mechanisms underpinning their tissue-specific phenotypes.
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