Uenoyama Atsuko, Miyata Makoto
Department of Biology, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan.
J Bacteriol. 2005 Aug;187(16):5578-84. doi: 10.1128/JB.187.16.5578-5584.2005.
Mycoplasma mobile glides on a glass surface in the direction of its tapered end by an unknown mechanism. Two large proteins, Gli349 and Gli521, were recently reported to be involved in glass binding and force generation/transmission, respectively, in M. mobile gliding. These proteins are coded tandemly with two other open reading frames (ORFs) in the order p123-gli349-gli521-p42 on the genome. In the present study, reverse transcriptase PCR analysis suggested that these four ORFs are transcribed cistronically. To characterize the p123 gene coding a 123-kDa protein (Gli123) of 1,128 amino acids, we raised polyclonal antibody against the Gli123 protein. Immunoblotting for Gli123 revealed that Gli123 was missing in a mutant strain, m12, which was previously isolated and characterized by a deficiency in glass binding. Sequencing analysis showed a nonsense mutation at the 523rd amino acid of the protein in the m12 mutant. Immunofluorescence microscopy with the polyclonal antibody showed that Gli123 is localized at the head-like protrusion's base, the cell neck, which is specialized for gliding, as observed for Gli349 and Gli521. Localization of the gliding proteins, Gli349 and Gli521, was disturbed in the m12 mutant, suggesting that Gli123 is essential for the positioning of gliding proteins in the cell neck.
移动支原体通过未知机制在玻璃表面朝着其锥形末端滑行。最近有报道称,两种大蛋白Gli349和Gli521分别参与移动支原体滑行过程中的玻璃结合以及力的产生/传递。这些蛋白在基因组上与另外两个开放阅读框(ORF)串联编码,顺序为p123 - gli349 - gli521 - p42。在本研究中,逆转录酶PCR分析表明这四个ORF是顺反子转录的。为了表征编码1128个氨基酸的123 kDa蛋白(Gli123)的p123基因,我们制备了针对Gli123蛋白的多克隆抗体。对Gli123的免疫印迹分析显示,在先前分离并鉴定为缺乏玻璃结合能力的突变株m12中,Gli123缺失。测序分析表明,m12突变体中该蛋白的第523个氨基酸处存在无义突变。用多克隆抗体进行的免疫荧光显微镜检查显示,Gli123定位于头部样突起的基部,即细胞颈部,这是专门用于滑行的部位,就像Gli349和Gli521的情况一样。在m12突变体中,滑行蛋白Gli349和Gli521的定位受到干扰,这表明Gli123对于滑行蛋白在细胞颈部的定位至关重要。