Glew M D, Baseggio N, Markham P F, Browning G F, Walker I D
Department of Veterinary Science, The University of Melbourne, Parkville, Victoria, Australia 3052.
Infect Immun. 1998 Dec;66(12):5833-41. doi: 10.1128/IAI.66.12.5833-5841.1998.
We analyzed the segment of DNA which contains the expressed pMGA gene from one strain of Mycoplasma gallisepticum in normal (strain S6) cells and in cells in which pMGA1.1 gene expression had ceased as a consequence of in vitro culture in the presence of pMGA1. 1-specific antibodies. Sequence analysis of isolates lacking pMGA1.1 expression revealed that this gene, which is typically expressed, exhibited sequence changes within a region 5' to its promoter. Specifically, pMGA1.1(+) cells contained a (GAA)12 motif upstream of the promoter, whereas in pMGA1.1(-) cells the corresponding region contained a (GAA)10 motif; when such cells were grown in medium no longer containing pMGA-specific antibodies, pMGA1.1 was reexpressed and the 5' (GAA)12 motif was restored. Two other genes, pMGA1.9 and pMGA1.2, were also shown to acquire a (GAA)12 motif in clones which expressed these genes. The results imply the evolution by the pMGA genes of M. gallisepticum of a novel transcriptional requirement which facilitates rapid and reversible switches in the pMGA expression pattern.
我们分析了来自一株鸡毒支原体的包含已表达的pMGA基因的DNA片段,该片段存在于正常(S6株)细胞中,以及因在存在pMGA1.1特异性抗体的情况下进行体外培养而导致pMGA1.1基因表达停止的细胞中。对缺乏pMGA1.1表达的分离株进行序列分析发现,这个通常表达的基因在其启动子5'端的一个区域内出现了序列变化。具体而言,pMGA1.1(+)细胞在启动子上游含有一个(GAA)12基序,而在pMGA1.1(-)细胞中,相应区域含有一个(GAA)10基序;当这些细胞在不再含有pMGA特异性抗体的培养基中生长时,pMGA1.1重新表达,5'端(GAA)12基序得以恢复。另外两个基因pMGA1.9和pMGA1.2在表达这些基因的克隆中也显示获得了一个(GAA)12基序。这些结果表明鸡毒支原体的pMGA基因进化出了一种新的转录需求,这种需求促进了pMGA表达模式的快速和可逆转换。