Dieci Giorgio, Fiorino Gloria, Castelnuovo Manuele, Teichmann Martin, Pagano Aldo
Dipartimento di Biochimica e Biologia Molecolare, Università degli Studi di Parma, Viale G.P. Usberti 23/A, 43100 Parma, Italy.
Trends Genet. 2007 Dec;23(12):614-22. doi: 10.1016/j.tig.2007.09.001. Epub 2007 Oct 30.
The role of RNA polymerase (Pol) III in eukaryotic transcription is commonly thought of as being restricted to a small set of highly expressed, housekeeping non-protein-coding (nc)RNA genes. Recent studies, however, have remarkably expanded the set of known Pol III-synthesized ncRNAs, suggesting that gene-specific Pol III regulation is more common than previously appreciated. Newly identified Pol III transcripts include small nucleolar RNAs, microRNAs, short interspersed nuclear element-encoded or tRNA-derived RNAs and novel classes of ncRNA that can display significant sequence complementarity to protein-coding genes and might thus regulate their expression. The extent of the Pol III transcriptome, the complexity of its regulation and its influence on cell physiology, development and disease are emerging as new areas for future research.
RNA聚合酶(Pol)III在真核生物转录中的作用通常被认为局限于一小部分高表达的管家非蛋白质编码(nc)RNA基因。然而,最近的研究显著扩展了已知的由Pol III合成的ncRNA集合,这表明基因特异性的Pol III调控比以前认为的更为普遍。新鉴定出的Pol III转录本包括小核仁RNA、微小RNA、短散在核元件编码的或tRNA衍生的RNA,以及一类新的ncRNA,它们可能与蛋白质编码基因具有显著的序列互补性,从而可能调控其表达。Pol III转录组的范围、其调控的复杂性及其对细胞生理学、发育和疾病的影响正成为未来研究的新领域。