Halbreich A, Grandchamp C, Foucher M
Eur J Biochem. 1984 Oct 15;144(2):261-9. doi: 10.1111/j.1432-1033.1984.tb08459.x.
bI1 RNA (excised from the first intron of the long form of the cytochrome b gene of Saccharomyces cerevisiae mitochondria) hybridizes with the two strands of a Bg/II-MboI DNA segment from this region. This fraction is resistant to digestions by DNase I and RNase T1 and disappears completely upon alkali hydrolysis. Strand-specific labeling of an intronic DNA fragment, cloned in pBR322 plasmid, was accomplished through the use of a T4 DNA polymerase. The purity of the probes was demonstrated by cloning an exon-intron fragment and labeling it by the same procedure; mRNA and pre-mRNA bands hybridized only with the transcribed DNA strand whereas bI1 RNA hybridized with the two strands under the stringent washing conditions employed (tm + 20 degrees C). Several experimental results argue against the possibility that the observation of two complementary bI1 RNA strands results from a partial self-complementarity of the RNA. A pre-mRNA intermediate from a box8 (G5046) mutant, still containing this intron, hybridizes only with the transcribed DNA strand of the pure intronic probe. The amount of the non-sense bI1 RNA strand is very low, in cells from two wild-type strains, relative to the sense RNA strand during the early stages of growth on glucose. It increases as the cells are released from glucose repression. bI1 RNA is resistant to RNase. Very little self-complementarity is seen by computer analysis of the sequence. Purified bI1 RNA is seen by electron microscopy under non-denaturing conditions as a mixture of double-stranded circular and linear molecules thus confirming the existence of the two complementary strands. The disappearance of all material following alkali hydrolysis demonstrates that these are indeed two RNA strands. Under fully denaturing conditions a mixture of single-stranded circular and linear molecules is seen as reported previously (Cell, 19, 321-329, 1980). We conclude that yeast mitochondria contain the two complementary bI1 RNA strands, one circular and the other linear. Considering a largely asymmetrical transcription of the mitochondrial genome in yeast and assuming that circularization of some intronic RNAs is part of RNA processing, we do not believe that the two strands are each a mixture of linear and circular molecules. The ratio of non-sense to sense bI1 RNA in a cytoplasmic petite mutant, A1B1, also varies according to growth conditions.(ABSTRACT TRUNCATED AT 400 WORDS)
bI1 RNA(从酿酒酵母线粒体细胞色素b基因长形式的第一个内含子中切除)与该区域的Bg/II - MboI DNA片段的两条链杂交。该部分对DNase I和RNase T1消化具有抗性,并且在碱水解后完全消失。通过使用T4 DNA聚合酶,完成了克隆在pBR322质粒中的内含子DNA片段的链特异性标记。通过克隆一个外显子 - 内含子片段并以相同程序进行标记,证明了探针的纯度;mRNA和前体mRNA条带仅与转录的DNA链杂交,而bI1 RNA在所用的严格洗涤条件下(tm + 20摄氏度)与两条链杂交。几个实验结果反对观察到两条互补的bI1 RNA链是由于RNA的部分自我互补性这一可能性。来自box8(G5046)突变体的仍含有该内含子的前体mRNA中间体仅与纯内含子探针的转录DNA链杂交。在葡萄糖上生长的早期阶段,相对于有义RNA链,来自两个野生型菌株细胞中的无义bI1 RNA链的量非常低。随着细胞从葡萄糖阻遏中释放,其增加。bI1 RNA对RNase具有抗性。通过对序列的计算机分析,几乎看不到自我互补性。在非变性条件下,通过电子显微镜观察纯化的bI1 RNA,其为双链环状和线性分子的混合物,从而证实了两条互补链的存在。碱水解后所有物质的消失表明这些确实是两条RNA链。在完全变性条件下,如先前报道(《细胞》,19,321 - 329,1980),观察到单链环状和线性分子的混合物。我们得出结论,酵母线粒体包含两条互补的bI1 RNA链,一条是环状的,另一条是线性的。考虑到酵母中线粒体基因组的转录在很大程度上是不对称的,并假设一些内含子RNA的环化是RNA加工的一部分,我们不认为这两条链各自是线性和环状分子的混合物。细胞质小菌落突变体A1B1中无义与有义bI1 RNA的比例也根据生长条件而变化。(摘要截于400字)