Wang L, Weiss B
Department of Pathology, University of Michigan Medical School, Ann Arbor 48109-0602.
J Bacteriol. 1992 Sep;174(17):5647-53. doi: 10.1128/jb.174.17.5647-5653.1992.
In Escherichia coli, most of the dUMP that is used as a substrate for thymidylate synthetase is generated from dCTP through the sequential action of dCTP deaminase and dUTPase. Some mutations of the dut (dUTPase) gene are lethal even when the cells are grown in the presence of thymidine, but their lethality can be suppressed by extragenic mutations that can be produced by transposon insertion. Six suppressor mutations were tested, and all were found to belong to the same complementation group. The affected gene was cloned, it was mapped by hybridization with a library of recombinant DNA, and its nucleotide sequence was determined. The gene is at 2,149 kb on the physical map. Its product, a 21.2-kDa polypeptide, was overproduced 1,000-fold via an expression vector and identified as dCTP deaminase, the enzyme affected in previously described dcd mutants. Null mutations in dcd probably suppress the lethality of dut mutations by reducing the accumulation of dUTP, which would otherwise lead to the excessive incorporation of uracil into DNA.
在大肠杆菌中,用作胸苷酸合成酶底物的大部分脱氧尿苷一磷酸(dUMP)是通过dCTP脱氨酶和dUTPase的顺序作用从dCTP生成的。dut(dUTPase)基因的一些突变即使在细胞于胸苷存在下生长时也是致死的,但其致死性可被转座子插入产生的基因外突变所抑制。测试了六个抑制突变,发现它们都属于同一互补群。受影响的基因被克隆,通过与重组DNA文库杂交进行定位,并确定了其核苷酸序列。该基因在物理图谱上位于2149kb处。其产物是一种21.2kDa的多肽,通过表达载体过量表达了1000倍,并被鉴定为dCTP脱氨酶,该酶在先前描述的dcd突变体中受到影响。dcd中的无效突变可能通过减少dUTP的积累来抑制dut突变的致死性,否则dUTP会导致尿嘧啶过度掺入DNA中。