Dixon Kevin, Bayliss Christopher D, Makepeace Katherine, Moxon E Richard, Hood Derek W
University of Oxford, John Radcliffe Hospital, UK.
J Bacteriol. 2007 Jan;189(2):511-21. doi: 10.1128/JB.00815-06. Epub 2006 Nov 10.
Simple sequence repeats located within reading frames mediate phase-variable ON/OFF switches in gene expression by generating frameshifts. Multiple translation initiation codons in different reading frames are found upstream of most Haemophilus influenzae tetranucleotide repeat tracts, raising the possibility of multiple active reading frames and more than two levels of gene expression for these loci. Phase variation between three levels of gene expression (strong, weak, and none) was observed when lic2A was fused to a lacZ reporter gene. The lic2A 5' CAAT repeat tract is preceded by four 5' ATG codons (x, y, z1, and z2) in two reading frames. Each of these initiation codons was inactivated by site-directed mutagenesis. Strong expression from frame 1 was associated with x but not y. Weak expression from frame 2 was mainly dependent on the z2 codon, and there was no expression from frame 3. Using monoclonal antibodies specific for a digalactoside epitope of lipopolysaccharide whose synthesis requires Lic2A, two levels (strong and undetectable) of antibody reactivity were detected, suggesting that weak expression of lic2A is not discernible at the phenotypic level. Inactivation of the x initiation codon resulted in loss of strong expression of the digalactoside epitope and elevated killing by human serum. The failure to detect more than two phenotypes for lic2A, despite clear evidence of weak expression from the z1/z2 initiation codons, leaves open the question of whether or not multiple initiation codons are associated with more complex patterns of phenotypic variation rather than classical phase-variable switching between two phenotypes.
位于阅读框内的简单序列重复通过产生移码来介导基因表达中的相位可变开/关开关。在大多数流感嗜血杆菌四核苷酸重复序列上游发现了不同阅读框中的多个翻译起始密码子,这增加了这些基因座存在多个活性阅读框和超过两个基因表达水平的可能性。当 lic2A 与 lacZ 报告基因融合时,观察到了基因表达三个水平(强、弱和无)之间的相位变异。lic2A 的 5' CAAT 重复序列之前在两个阅读框中有四个 5' ATG 密码子(x、y、z1 和 z2)。通过定点诱变使这些起始密码子中的每一个失活。来自阅读框 1 的强表达与 x 相关而与 y 无关。来自阅读框 2 的弱表达主要依赖于 z2 密码子,阅读框 3 没有表达。使用针对脂多糖二半乳糖苷表位的单克隆抗体(其合成需要 Lic2A),检测到了两个水平(强和不可检测)的抗体反应性,这表明 lic2A 的弱表达在表型水平上无法辨别。x 起始密码子的失活导致二半乳糖苷表位的强表达丧失以及人血清杀伤作用增强。尽管有明确证据表明 z1/z2 起始密码子有弱表达,但未能检测到 lic2A 有超过两种表型,这就留下了一个问题,即多个起始密码子是否与更复杂的表型变异模式相关,而不是与两种表型之间的经典相位可变开关相关。