Flitman-Tene Ravenna, Mudahi-Orenstein Sigalit, Levisohn Sharon, Yogev David
Department of Membrane and Ultrastructure Research, The Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel.
Infect Immun. 2003 Jul;71(7):3821-30. doi: 10.1128/IAI.71.7.3821-3830.2003.
Mycoplasma agalactiae, the etiological agent of contagious agalactia of small ruminants, has a family of related genes (avg genes) which encode surface lipoprotein antigens that undergo phase variation. A series of 13 M. agalactiae clonal isolates, obtained from one chronically infected animal over a period of 7 months, were found to undergo major rearrangement events within the avg genomic locus. We show that these rearrangements regulate the phase-variable expression of individual avg genes. Northern blot analysis and reverse transcription-PCR showed that only one avg gene is transcribed, while the other avg genes are transcriptionally silent. Sequence analysis and primer extension experiments with two M. agalactiae clonal isolates showed that a specific 182-bp avg 5' upstream region (avg-B(2)) that is present as a single chromosomal copy serves as an active promoter and exhibits a high level of homology with the vsp promoter of the bovine pathogen Mycoplasma bovis. PCR analysis showed that each avg gene is associated with the avg-B(2) promoter in a subpopulation of cells that is present in each subclone. Multiple sequence-specific sites for DNA recombination (vis-like), which are presumably recognized by site-specific recombinase, were identified within the conserved avg 5' upstream regions of all avg genes and were found to be identical to the recombination sites of the M. bovis vsp locus. In addition, a gene encoding a member of the integrase family of tyrosine site-specific recombinases was identified adjacent to the variable avg locus. The molecular genetic basis for avg phase-variable expression appears to be mediated by site-specific DNA inversions occurring in vivo that allow activation of a silent avg gene by promoter addition. A model for the control of avg genes is proposed.
无乳支原体是小反刍动物传染性无乳症的病原体,它有一组相关基因(avg基因),这些基因编码会发生相变的表面脂蛋白抗原。从一只慢性感染动物身上在7个月内获取的一系列13株无乳支原体克隆分离株,被发现在avg基因组位点内发生了重大重排事件。我们表明,这些重排调节了单个avg基因的相变表达。Northern印迹分析和逆转录PCR表明,只有一个avg基因被转录,而其他avg基因转录沉默。对两株无乳支原体克隆分离株的序列分析和引物延伸实验表明,作为单个染色体拷贝存在的一个特定的182 bp的avg 5'上游区域(avg-B(2))作为一个活性启动子,并且与牛病原体牛支原体的vsp启动子具有高度同源性。PCR分析表明,每个avg基因在每个亚克隆中存在的细胞亚群中与avg-B(2)启动子相关联。在所有avg基因保守的5'上游区域内鉴定出了多个可能被位点特异性重组酶识别的DNA重组序列特异性位点(vis样),并且发现它们与牛支原体vsp位点的重组位点相同。此外,在可变的avg位点附近鉴定出了一个编码酪氨酸位点特异性重组酶整合酶家族成员的基因。avg相变表达的分子遗传基础似乎是由体内发生的位点特异性DNA倒位介导的,这种倒位通过添加启动子使沉默的avg基因激活。提出了一个控制avg基因的模型。