Doermann A H, Pao A, Jackson P
J Virol. 1987 Sep;61(9):2823-7. doi: 10.1128/JVI.61.9.2823-2827.1987.
Fifty-two new bacteriophage T4 ptg mutations have been isolated by selecting for the giant-capsid phenotype they display. Genetic mapping placed all of them at eight sites, all located in gene 23. These sites were clustered in three locations, one near amber B17 (gene 23 nucleotide [NT] 268), another centrally placed between amE506 (NT 706) and amE1270 (NT 925), and the third between amC208 (NT 1297) and amE1236 (NT 1489). The lack of a selective system for identifying recombinant genotypes when dealing with the very close linkages found within these clusters opens the possibility that more than eight sites are represented in this set of mutations. Since one site was represented by only one mutation, it seems likely that further searching might uncover additional sites. It is suggested that the clustering of mutations observed here identifies regions of the gene 23 product that play a role in regulating the capsid length of T4.
通过选择它们所表现出的巨大衣壳表型,已分离出52个新的噬菌体T4 ptg突变。遗传图谱将它们全部定位在8个位点,所有这些位点都位于基因23中。这些位点聚集在三个位置,一个靠近琥珀型B17(基因23核苷酸[NT] 268),另一个位于amE506(NT 706)和amE1270(NT 925)之间的中心位置,第三个位于amC208(NT 1297)和amE1236(NT 1489)之间。在处理这些簇内发现的非常紧密的连锁关系时,缺乏用于鉴定重组基因型的选择系统,这使得在这组突变中可能存在超过8个位点。由于一个位点仅由一个突变代表,进一步搜索似乎可能会发现其他位点。有人认为,此处观察到的突变聚集确定了基因23产物中在调节T4衣壳长度方面起作用的区域。