Alexandersen S, Bloom M E, Perryman S
National Institute of Allergy and Infectious Diseases, Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, Hamilton, Montana 59840.
J Virol. 1988 Oct;62(10):3684-94. doi: 10.1128/JVI.62.10.3684-3694.1988.
We studied the transcription program of Aleutian mink disease parvovirus (ADV) by using a combination of cDNA cloning and sequencing, primer extension, and Northern (RNA) blot hybridization with splice-specific oligonucleotides. The 4.8-kilobase ADV genome was transcribed in the rightward direction, yielding plus-sense polyadenylated transcripts of 4.3 (R1 RNA), 2.8 (R2), 2.8 (R3), 1.1 (RX), and 0.85 (R2') kilobases. Each RNA transcript had potential translation initiation sites within open reading frames, suggesting protein translation, and a scheme encompassing ADV structural and nonstructural proteins is proposed. Each of the five RNA transcripts had a characteristic set of splices and originated from a promoter at nucleotide 152 (map unit 3 [R1, R2, R2', and RX]) or at nucleotide 1729 (map unit 36 [R3]). The transcripts terminated with a poly(A) tail at one of two positions: either at map unit 53 (R2' and RX) or at map unit 92 (R1, R2, and R3). Similarities with and differences from the transcription maps of other parvoviruses are discussed, and possible roles of the unique features found in ADV transcription are related to the special pathogenic features of this virus.
我们通过结合cDNA克隆与测序、引物延伸以及使用剪接特异性寡核苷酸进行Northern(RNA)印迹杂交,研究了阿留申水貂病细小病毒(ADV)的转录程序。4.8千碱基的ADV基因组以向右的方向转录,产生了4.3(R1 RNA)、2.8(R2)、2.8(R3)、1.1(RX)和0.85(R2')千碱基的正义多聚腺苷酸化转录本。每个RNA转录本在开放阅读框内都有潜在的翻译起始位点,提示有蛋白质翻译,并提出了一个涵盖ADV结构蛋白和非结构蛋白的方案。五个RNA转录本中的每一个都有一组独特的剪接方式,并且起源于核苷酸152(图谱单位3 [R1、R2、R2'和RX])或核苷酸1729(图谱单位36 [R3])处的启动子。转录本在两个位置之一处终止于一个多聚(A)尾:要么在图谱单位53(R2'和RX)处,要么在图谱单位92(R1、R2和R3)处。讨论了与其他细小病毒转录图谱的异同,并且ADV转录中发现的独特特征的可能作用与该病毒的特殊致病特征相关。