Tseng M J, Hilfinger J M, Walsh A, Greenberg G R
Department of Biological Chemistry, University of Michigan, Ann Arbor 48109-0606.
J Biol Chem. 1988 Nov 5;263(31):16242-51.
As a part of a study of the role of bacteriophage T4-coded ribonucleoside diphosphate reductase in the switch-on and regulation of T4 DNA replication, we report the cloning and sequencing of the nrdA gene, coding for the alpha protein chain of the enzyme. The open reading frame of the nrdA gene begins 558 base pairs downstream of the 3' terminus of the td gene (thymidylate synthase). nrdB, encoding the beta chain of the enzyme, initiates 700 base pairs from the termination of nrdA. A high degree of similarity is found between the deduced amino acid sequence of the 754-residue alpha chain and the corresponding chain reported for nrdA of Escherichia coli; 56% of the residues are identical, with some segments reaching 84%. Some structural aspects of the derived alpha 2 subunit of the T4 enzyme are explored. By the S1 nuclease protection method, the RNA formed after T4 infection contains two prereplicative transcripts for nrdA, T3 and TU, and one postreplicative transcript, TL. T3 is found in low concentration. While the 5' termini of T3 and TL occur at sites near nrdA, TU apparently is a multicistronic transcript initiating farther upstream. The regulation of nrdA expression is examined in light of these findings.
作为噬菌体T4编码的核糖核苷二磷酸还原酶在T4 DNA复制的启动和调控中作用研究的一部分,我们报道了编码该酶α蛋白链的nrdA基因的克隆和测序。nrdA基因的开放阅读框始于td基因(胸苷酸合成酶)3'末端下游558个碱基对处。编码该酶β链的nrdB基因起始于距nrdA终止处700个碱基对。在推导的754个氨基酸残基的α链氨基酸序列与报道的大肠杆菌nrdA相应链之间发现高度相似性;56%的残基相同,有些片段高达84%。对T4酶衍生的α2亚基的一些结构方面进行了探索。通过S1核酸酶保护法,T4感染后形成的RNA包含nrdA的两个复制前转录本T3和TU,以及一个复制后转录本TL。T3浓度较低。虽然T3和TL的5'末端出现在nrdA附近的位点,但TU显然是一个起始于更上游的多顺反子转录本。根据这些发现对nrdA表达的调控进行了研究。