Martins A, Ribeiro G, Marques M I, Costa J V
Laboratory of Virology II, Gulbenkian Institute of Science, Oeiras, Portugal.
Nucleic Acids Res. 1994 Jan 25;22(2):208-13. doi: 10.1093/nar/22.2.208.
The DNA polymerase gene of African swine fever virus (ASFV) was mapped by marker rescue experiments using a phosphonoacetic acid-resistant mutant and hybridization with an oligonucleotide probe designed from the most conserved motif of family B DNA polymerases. Viral DNA fragments mapping in this region were cloned and sequenced. An open reading frame coding for a 1244 amino acid long peptide with a molecular mass of 142.5 kDa was determined from the sequence. A unique feature of ASFV DNA polymerase is the presence of 13 tandem repeats of the sequence Ala-Gly-Asp-Pro near the carboxyl end of the molecule. Comparison with 30 sequences of alpha-like DNA polymerases of cellular and viral origin showed that ASFV DNA polymerase has all the conserved motifs of family B DNA polymerases. A 3.9 kb transcript was detected by Northern hybridization and the transcription initiation and termination sites were mapped by S1 analysis and primer extension. Late transcription was initiated at a site different from the early transcription initiation site. A 145 kDa protein, consistent with the size of the gene, was identified by an in situ enzyme assay after gel electrophoresis of infected cell extracts.
利用耐膦酰乙酸突变体通过标记拯救实验以及与根据B族DNA聚合酶最保守基序设计的寡核苷酸探针杂交,对非洲猪瘟病毒(ASFV)的DNA聚合酶基因进行了定位。对定位在该区域的病毒DNA片段进行了克隆和测序。从序列中确定了一个编码1244个氨基酸长肽、分子量为142.5 kDa的开放阅读框。ASFV DNA聚合酶的一个独特特征是在分子羧基末端附近存在13个Ala-Gly-Asp-Pro序列的串联重复。与30个细胞和病毒来源的α样DNA聚合酶序列进行比较表明,ASFV DNA聚合酶具有B族DNA聚合酶的所有保守基序。通过Northern杂交检测到一个3.9 kb的转录本,并通过S1分析和引物延伸确定了转录起始和终止位点。晚期转录起始于一个与早期转录起始位点不同的位点。在对感染细胞提取物进行凝胶电泳后,通过原位酶测定法鉴定出一种与基因大小相符的145 kDa蛋白质。