Jolly D J, Thomas C A
Nucleic Acids Res. 1980 Jan 11;8(1):67-84. doi: 10.1093/nar/8.1.67.
The transcription of ribosomal genes in a cell line (Kc) derived from female D.melanogaster, has been investigated using hybridization probes prepared from restriction fragments of a cloned rDNA repeat with a 5 kb type I [Wellauer et al. (1978) Cell 14, 269-278] intron. Gels, of nuclear RNA that have been transferred to diazotized paper and hybridized with labelled intron sequences, reveal both large (1-10 kb) transcripts and a discrete 325 base species. Berk-Sharp experiments [(1977) Cell 12, 721-732] reveal large transcripts that are homologous to intron sequences and extend into 28S sequences as well. However, while the abundance of 28S transcripts is about 50,000 copies per nucleus [Clark et al. (1977) Genetics 86, 789-800], these long transcripts are only present at 1-2 copies per nucleus and the 325 base species is only 10 times more abundant. In view of the fact that female cells have about 400 rDNA genes, 49% of which have type I introns, one must conclude either that transcription rarely occurs from the genes containing introns (the majority) or these transcripts are processed unusually rapidly. Transcripts homologous to the "non-transcribed spacer" region have been found, but their abundance is no higher.
利用从含有5 kb I型内含子的克隆rDNA重复序列的限制性片段制备的杂交探针,对源自雌性黑腹果蝇的细胞系(Kc)中的核糖体基因转录进行了研究。转移到重氮化纸上并与标记的内含子序列杂交的核RNA凝胶显示出大的(1 - 10 kb)转录本和一个离散的325个碱基的物种。伯克 - 夏普实验[(1977年)《细胞》12卷,721 - 732页]显示出与内含子序列同源且延伸到28S序列的大转录本。然而,虽然28S转录本的丰度约为每个细胞核50,000个拷贝[克拉克等人(1977年)《遗传学》86卷,789 - 800页],但这些长转录本每个细胞核仅以1 - 2个拷贝存在,且325个碱基的物种仅丰富10倍。鉴于雌性细胞约有400个rDNA基因,其中49%含有I型内含子,人们必须得出这样的结论:要么转录很少发生在含有内含子的基因(大多数)上,要么这些转录本的加工异常迅速。已发现与“非转录间隔区”区域同源的转录本,但其丰度并不更高。