Hogan N C, Traverse K L, Sullivan D E, Pardue M L
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
J Cell Biol. 1994 Apr;125(1):21-30. doi: 10.1083/jcb.125.1.21.
The Drosophila Hsr-omega puff, one of the largest heat shock puffs, reveals a very unusual gene, identified by heat shock but constitutively active in nearly all cell types. Surprisingly, Hsr-omega yields two transcription end-products with very different roles. The larger, omega-n, is a nuclear RNA with characteristics suggesting a new class of nuclear RNAs. Although it neither leaves the nucleus nor undergoes processing, omega-n RNA is polyadenylated, showing that polyadenylation is not limited to cytoplasmic RNA, but possibly has a function in the nucleus. The amount of omega-n within the nucleus is specifically regulated by both transcription and turnover. Heat shock and several other agents cause rapid increases in omega-n. A rapid return to constitutive levels follows withdrawal of the agents. Degradation of omega-n is inhibited by actinomycin D, suggesting a novel intranuclear mechanism for RNA turnover. Within the nucleus, some omega-n RNA is concentrated at the transcription site; however, most is evenly distributed over the nucleus, showing no evidence of a concentration gradient which might be produced by simple diffusion from the site of transcription. Previous studies suggested that omega-n has a novel regulatory role in the nucleus. The actinomycin D-sensitive degradation system makes possible rapid changes in the amount of omega-n, allowing the putative regulatory activities to reflect cellular conditions at a given time. Omega-n differs from the best studied nuclear RNAs, snRNAs, in many ways. Omega-n demonstrates the existence of intranuclear mechanisms for RNA turnover and localization that may be used by a new class of nuclear RNAs.
果蝇的Hsr-ω胀泡是最大的热休克胀泡之一,它揭示了一个非常特殊的基因,该基因通过热休克鉴定,但在几乎所有细胞类型中都组成性活跃。令人惊讶的是,Hsr-ω产生两种具有截然不同作用的转录终产物。较大的ω-n是一种核RNA,其特征表明它是一类新的核RNA。尽管它既不离开细胞核也不进行加工,但ω-n RNA是多聚腺苷酸化的,这表明多聚腺苷酸化并不局限于细胞质RNA,而是可能在细胞核中具有功能。细胞核内ω-n的量受到转录和周转的特异性调节。热休克和其他几种因素会导致ω-n迅速增加。去除这些因素后,它会迅速恢复到组成性水平。放线菌素D抑制ω-n的降解,这表明存在一种新的核内RNA周转机制。在细胞核内,一些ω-n RNA集中在转录位点;然而,大多数均匀分布在细胞核中,没有显示出可能由转录位点简单扩散产生的浓度梯度的证据。先前的研究表明,ω-n在细胞核中具有新的调节作用。放线菌素D敏感的降解系统使ω-n的量能够快速变化,从而使假定的调节活性能够反映给定时间的细胞状况。ω-n在许多方面与研究得最透彻的核RNA即小核RNA(snRNA)不同。ω-n证明了核内存在RNA周转和定位机制,这些机制可能被一类新的核RNA所利用。