Rogiers R, van de Voorde A, Soeda E, Fiers W
Eur J Biochem. 1978 Apr;85(1):205-24. doi: 10.1111/j.1432-1033.1978.tb12229.x.
The restriction fragment Hind-K represents 4.2% of the genome of Simian virus 40 (SV40) and is located near the middle of the late region. Its nucleotide sequence is reported here. It was mainly established by analysis of transcription products, synthesized by means of Escherichia coli RNA polymerase and nucleoside triphosphates, one of which was (alpha-32P)-labeled. Strand assignment was possible by hybridization of asymmetric, labeled transcripts of total SV40 DNA to filter-bound Hind-K fragment. Further information and unambiguous confirmation of the sequence was obtained by the use of direct DNA-sequencing methods. For this purpose the fragment was labeled at the 5' ends by means of polynucleotide kinase and [gamma-32P]ATP and redigested with a suitable restriction enzyme. The separated products were then either partially digested with snake venom diesterase for analysis by the 'wandering spot' method or partially degraded with the base-specific reagents dimethylsulphate or hydrazine for direct sequence analysis on gel. The Hind-K sequence is 219 base pairs long. The message strand is particularly rich in adenosine (39%) and purines. The nucleotide sequence cna unambiguously be translated into an amino acid sequence and the N-terminal codon of the viral protein VP1 gene could be identified. The amino-terminal part of VP1 is rich in proline and lysine. The nucleotide sequence of Hind-K codes also for the carboxyl-terminal part of the viral protein VP2 and VP3 genes, which partly overlap the VP1 gene.
限制性片段Hind-K占猴病毒40(SV40)基因组的4.2%,位于晚期区域中部附近。本文报道了其核苷酸序列。它主要是通过分析转录产物确定的,转录产物由大肠杆菌RNA聚合酶和核苷三磷酸合成,其中一种核苷三磷酸是(α-32P)标记的。通过将SV40总DNA的不对称标记转录本与固定在滤膜上的Hind-K片段杂交,可以确定链的归属。通过使用直接DNA测序方法获得了进一步的信息并明确证实了序列。为此,该片段通过多核苷酸激酶和[γ-32P]ATP在5'端进行标记,然后用合适的限制性酶再次消化。然后,分离的产物要么用蛇毒磷酸二酯酶进行部分消化,通过“游动斑点”法进行分析,要么用碱基特异性试剂硫酸二甲酯或肼进行部分降解,以便在凝胶上进行直接序列分析。Hind-K序列长219个碱基对。编码链特别富含腺苷(39%)和嘌呤。核苷酸序列可以明确地翻译成氨基酸序列,并且可以鉴定病毒蛋白VP1基因的N端密码子。VP1的氨基末端部分富含脯氨酸和赖氨酸。Hind-K的核苷酸序列还编码病毒蛋白VP2和VP3基因的羧基末端部分,它们部分与VP1基因重叠。