Furdon P J, Guerrier-Takada C, Altman S
Nucleic Acids Res. 1983 Mar 11;11(5):1491-505. doi: 10.1093/nar/11.5.1491.
A novel mutation in the anticodon stem of E. coli tRNA1Tyrsu3+ (G43 to U43) has been characterized. The gene coding for the mutant tRNA, carried by phage phi 80DHA61.3 a derivative of phi 80psu3+su0, produces only 20% of mature suppressor tRNA as compared with phi 80psu3+. Both the mutant tRNA precursor and mature tRNA have an altered conformation. The precursor tRNA coded for by phi 80DHA61.3 is processed by RNase P more slowly than the su3+ precursor and does not form as stable an enzyme-substrate complex as does su3+ precursor. phi 80 DHA61.3 also contains a large deletion which begins in the spacer region between the su3+ gene and the su0- gene, extends through the su0- gene and includes most of the repeated region following the tRNA genes.
已对大肠杆菌tRNA1Tyrsu3+反密码子茎中的一种新型突变(G43突变为U43)进行了表征。由噬菌体phi 80DHA61.3(phi 80psu3+su0的衍生物)携带的编码突变tRNA的基因,与phi 80psu3+相比,仅产生20%的成熟抑制性tRNA。突变tRNA前体和成熟tRNA的构象均发生了改变。phi 80DHA61.3编码的前体tRNA被RNase P加工的速度比su3+前体慢,并且形成的酶-底物复合物不如su3+前体稳定。phi 80 DHA61.3还包含一个大的缺失,该缺失始于su3+基因和su0-基因之间的间隔区,延伸穿过su0-基因,并包括tRNA基因之后的大部分重复区域。