Markham P F, Glew M D, Whithear K G, Walker I D
School of Veterinary Science, University of Melbourne, Victoria, Australia.
Infect Immun. 1993 Mar;61(3):903-9. doi: 10.1128/iai.61.3.903-909.1993.
A hemagglutinin with an M(r) of 67,000 (pMGA) from Mycoplasma gallisepticum S6 was purified by using monoclonal antibody affinity chromatography. Purified pMGA was treated with a number of enzymes, the resultant peptides were purified, and their amino acid sequence was determined by using an Applied Biosystems (model 471A) protein sequencer. The DNA sequence encoding two peptides was used to dictate the sequences of synthetic oligonucleotides which were used to screen a library of EcoRI-cut M. gallisepticum DNA in pUC18. A clone reactive to both probes was isolated and found to contain a recombinant insert of 10 kb. The clone was mapped by using restriction endonucleases and fragments subcloned into pUC18 for DNA sequencing. Analysis of part of the DNA sequence revealed an open reading frame containing 1,941 nucleotides which encoded 647 amino acids. The amino terminus was preceded by a putative leader sequence of 25 amino acids. A promoter region preceding the putative start codon GUG was also located. This gene would encode a mature protein of 67,660 Da. There were a number of differences between the predicted amino acid sequence and that determined by direct peptide sequencing. Also, two tryptic peptides of pMGA were not found in the DNA sequence. This suggested that the cloned gene did not encode pMGA but did encode a homolog (pMGA1.2). Furthermore, downstream of pMGA1.2 was a region of DNA encoding a leader sequence followed by an amino acid sequence with high homology to that encoded by the pMGA1.2 gene. The presence within M. gallisepticum of a family of pMGA genes is inferred from the DNA sequence and Southern transfer data. A possible role for this gene family in immune evasion is discussed.
利用单克隆抗体亲和层析法对来自鸡毒支原体S6株的分子量为67,000的血凝素(pMGA)进行了纯化。将纯化后的pMGA用多种酶进行处理,对产生的肽段进行纯化,并使用应用生物系统公司(型号471A)的蛋白质测序仪测定其氨基酸序列。编码两个肽段的DNA序列被用于确定合成寡核苷酸的序列,这些寡核苷酸被用于筛选pUC18中经EcoRI酶切的鸡毒支原体DNA文库。分离出一个与两种探针均有反应的克隆,发现其含有一个10 kb的重组插入片段。使用限制性内切酶对该克隆进行图谱绘制,并将片段亚克隆到pUC18中进行DNA测序。对部分DNA序列的分析揭示了一个包含1941个核苷酸的开放阅读框,其编码647个氨基酸。氨基末端之前有一个25个氨基酸的假定前导序列。在假定的起始密码子GUG之前还定位到了一个启动子区域。该基因将编码一个分子量为67,660 Da的成熟蛋白。预测的氨基酸序列与直接肽段测序确定的序列存在一些差异。此外,在DNA序列中未发现pMGA的两个胰蛋白酶肽段。这表明克隆的基因不编码pMGA,而是编码一个同源物(pMGA1.2)。此外,在pMGA1.2的下游是一个DNA区域,其编码一个前导序列,随后是一个与pMGA1.2基因编码的氨基酸序列具有高度同源性的氨基酸序列。从DNA序列和Southern杂交数据推断鸡毒支原体中存在一个pMGA基因家族。讨论了该基因家族在免疫逃避中的可能作用。