Rhode S L, Paradiso P R
J Virol. 1983 Jan;45(1):173-84. doi: 10.1128/JVI.45.1.173-184.1983.
The nucleotide sequence of the parvovirus H-1 has been determined by the chain-terminating method of Sanger. The sequence is 5,176 nucleotides long. Two large open reading frames (1 and 2) and two smaller open reading frames (3 and 4) of potential importance were identified in the plus-strand sequence. Promoter sequences are located at map positions 4 and 38 when map positions are expressed as percent of genome length from the 3' end of the virion minus strand. The locations for the genes for the parvovirus capsid proteins and a 76,000-dalton noncapsid protein (NCVP1) were mapped by hybrid-arrested translation. The gene for the capsid proteins VP1 and VP2' is located in the 5' half of the virus genome. The gene for NCVP1 is located in the 3' half of the viral DNA.
细小病毒H-1的核苷酸序列已通过桑格的链终止法确定。该序列长度为5176个核苷酸。在正链序列中鉴定出两个具有潜在重要性的大开放阅读框(1和2)以及两个较小的开放阅读框(3和4)。当图谱位置表示为病毒粒子负链3'端基因组长度的百分比时,启动子序列位于图谱位置4和38处。通过杂交捕获翻译确定了细小病毒衣壳蛋白基因和一种76,000道尔顿非衣壳蛋白(NCVP1)的基因位置。衣壳蛋白VP1和VP2'的基因位于病毒基因组的5'半部分。NCVP1的基因位于病毒DNA的3'半部分。