Silberstein Z, Cohen A
J Bacteriol. 1978 Jun;134(3):1081-8. doi: 10.1128/jb.134.3.1081-1088.1978.
Transcribing Bacillus cereus DNA was visualized by means of autoradiography of electrophoretically separated EcoRI restriction endonuclease DNA fragments hybridizing 32P-labeled RNA. Hybridization of RNA of dormant spores, vegetative cells, and outgrowing spores indicates the following. (i) A large fraction of the nonribosomal RNA in dormant spores is transcribed at a limited number of regions on the bacterial chromosome. (ii) After induction of spore germination, transcription activity is not limited to a single short region on the chromosome, but rather is distributed along the chromosome. The DNA/RNA hybridization technique has been used to identify restriction endonuclease DNA fragments homologous to RNA species that are present in dormant spores but absent from vegetative cells, RNA species that are synthesized immediately after germination induction and are present at a relatively low concentration in vegetative cells, and RNA species that are transcribed at a late stage of outgrowth but are absent or present at low concentration at an early stage of outgrowth.
通过对经电泳分离的EcoRI限制性内切酶DNA片段与32P标记的RNA杂交进行放射自显影,来观察蜡样芽孢杆菌DNA的转录情况。休眠孢子、营养细胞和萌发孢子的RNA杂交结果表明如下:(i)休眠孢子中很大一部分非核糖体RNA是在细菌染色体上有限数量的区域转录的。(ii)诱导孢子萌发后,转录活性并不局限于染色体上的单个短区域,而是沿着染色体分布。DNA/RNA杂交技术已被用于鉴定与以下RNA种类同源的限制性内切酶DNA片段:存在于休眠孢子中但在营养细胞中不存在的RNA种类;萌发诱导后立即合成且在营养细胞中浓度相对较低的RNA种类;在生长后期转录但在生长早期不存在或浓度较低的RNA种类。