Childs G J, Freundlich M
Mol Gen Genet. 1975 Jun 19;138(3):257-68. doi: 10.1007/BF00269352.
Hybridization of messenger ribonucleic acid (mRNA) isolated from Escherichia Coli K-12 to deoxyribonucleic acid (DNA) from lambdaCI857st68h80dilv was used to detect isoleucine-valine (ilv) specific mRNA. A number of strains partially constitutive for the isoleucine-valine enzymes had levels of ilv mRNA 2 to 3-fold higher than the parent strain. Starvation for any of the branched-chain amino acids resulted in a 20 to 23-fold increase in ilv mRNA as compared to repressed levels. These differences were not due to altered growth rates or to changes in the stability of ilv mRNA. These data indicate that regulation of the isoleucine-valine enzymes by multivalent repression occurs mainly at the level of transcription. Kinetics of elongation of ilv mRNA after repression are consistent with the assumption that the mechanism of multivalent repression involves the prevention of further initiations by RNA polymerase.
从大肠杆菌K-12分离的信使核糖核酸(mRNA)与λCI857st68h80dilv的脱氧核糖核酸(DNA)杂交,用于检测异亮氨酸-缬氨酸(ilv)特异性mRNA。一些异亮氨酸-缬氨酸酶部分组成型的菌株,其ilv mRNA水平比亲本菌株高2至3倍。与阻遏水平相比,任何一种支链氨基酸饥饿都会导致ilv mRNA增加20至23倍。这些差异不是由于生长速率改变或ilv mRNA稳定性变化所致。这些数据表明,多价阻遏对异亮氨酸-缬氨酸酶的调节主要发生在转录水平。阻遏后ilv mRNA的延伸动力学与多价阻遏机制涉及防止RNA聚合酶进一步起始的假设一致。