Welkos S L, Holmes R K
J Virol. 1981 Mar;37(3):946-54. doi: 10.1128/JVI.37.3.946-954.1981.
The structural gene for diphtherial toxin is present in corynebacteriophage beta. Previous studies located several point mutations within the tox locus and determined the orientation of transcription of the toxin structural gene. The production of maximal quantities of toxin by Corynebacterium diphtheriae C7(beta) occurs only when the bacteria are iron deficient. Mutations in phage beta can affect this control of toxin production by iron. The tox-201 mutation regulates expression of the toxin structural gene in a cis-dominant manner and permits large amounts of toxin to be made under high-iron conditions when phage beta tox-201 infects C. diphtheriae C7. In this study tox-201 was found to be closely linked to the structural gene for toxin. We performed a series of multifactor matings to determine the relative positions of tox-201 and several point mutations within the toxin structural gene. The order of these markers on the vegetative genetic map of phage beta was tox-201-tox-4-tox-2-tox-30. These findings establish that the tox-201 regulatory site is closely linked to the end of the toxin structural gene corresponding to the origin of transcription. This location is consistent with our hypothesis that tox-201 defines a cis-dominant regulatory element, such as an operator, promoter, or attenuator, involved in control of toxinogenesis in C. diphtheriae C7(beta).
白喉毒素的结构基因存在于β棒状杆菌噬菌体中。先前的研究在tox基因座内定位了几个点突变,并确定了毒素结构基因的转录方向。只有当细菌缺铁时,白喉棒状杆菌C7(β)才能产生最大量的毒素。β噬菌体中的突变会影响铁对毒素产生的这种控制。tox - 201突变以顺式显性方式调节毒素结构基因的表达,当β噬菌体tox - 201感染白喉棒状杆菌C7时,在高铁条件下也能产生大量毒素。在本研究中,发现tox - 201与毒素的结构基因紧密连锁。我们进行了一系列多因子交配实验,以确定tox - 201与毒素结构基因内几个点突变的相对位置。这些标记在β噬菌体营养遗传图谱上的顺序是tox - 201 - tox - 4 - tox - 2 - tox - 30。这些发现表明,tox - 201调控位点与对应于转录起点的毒素结构基因末端紧密相连。这一位置与我们的假设一致,即tox - 201定义了一个顺式显性调控元件,如操纵子、启动子或衰减子,参与白喉棒状杆菌C7(β)毒素生成的控制。