Long E O, Collins M, Kiefer B I, Dawid I B
Mol Gen Genet. 1981;182(3):377-84. doi: 10.1007/BF00293925.
We have shown earlier that interrupted rRNA genes in Drosophila melanogaster do not contribute significantly to rRNA production by a splicing mechanism (Long and Dawid 1979). In the work reported here the expression of interrupted rRNA genes was tested in several stocks that carry bobbed mutations, i.e., have partial deletions of their rRNA gene clusters. Transcripts of the major 5 kb type 1 insertion are very rare in bobbed flies as they are in the wild type, occurring at a concentration in embryos of less than one copy per nucleus. Transcripts of short type 1 insertions are more abundant in certain bobbed stocks, especially those carrying the car bb chromosome. However, other severely bobbed flies have no increase in these insertion transcripts over the wild-type levels. Type 2 insertions are transcribed into very rare RNA molecules in the wild type and in the bobbed genotypes that were studied. From these results we conclude that interrupted rRNA genes are not expressed through a splicing mechanism into mature rRNA in mutant or wild-type flies. Since even severely bobbed flies fail to utilize their interrupted rRNA genes, we suggest that these genes cannot be transcribed productively in D. melanogaster.
我们之前已经表明,果蝇中中断的rRNA基因通过剪接机制对rRNA产生的贡献不大(Long和Dawid,1979年)。在本文报道的研究中,我们在几种带有截毛突变的品系中测试了中断的rRNA基因的表达情况,即这些品系的rRNA基因簇存在部分缺失。主要的5kb 1型插入片段的转录本在截毛果蝇中非常罕见,如同在野生型果蝇中一样,在胚胎中的浓度低于每个细胞核一个拷贝。短1型插入片段的转录本在某些截毛品系中更为丰富,特别是那些携带car bb染色体的品系。然而,其他严重截毛的果蝇中这些插入片段的转录本并没有比野生型水平增加。2型插入片段在野生型以及所研究的截毛基因型中都转录为非常罕见的RNA分子。从这些结果我们得出结论,在突变体或野生型果蝇中,中断的rRNA基因不会通过剪接机制表达为成熟的rRNA。由于即使是严重截毛的果蝇也无法利用其中断的rRNA基因,我们认为这些基因在黑腹果蝇中无法有效转录。