Auperin D D, Galinski M, Bishop D H
Virology. 1984 Apr 15;134(1):208-19. doi: 10.1016/0042-6822(84)90286-1.
Two overlapping DNA clones representing more than half of the Pichinde arenavirus S RNA segment were cloned into pBR322 and their nucleotide sequences were determined. The analyses predict that the viral nucleocapsid protein (N) is encoded in a reading frame in the viral complementary RNA sequence starting at viral S RNA nucleotide residue 84 from the 3' end and terminating with an opal codon at residues 1767-1769. The position of the termination codon has been confirmed by primer directed dideoxynucleotide sequencing. The N protein has a calculated size of 62,911 Da and a net positive charge of +9. Viral complementary 15 S mRNA that directs the synthesis of N protein and hybridizes to the predicted N gene DNA has been identified in infected cell extracts. A second nonoverlapping reading frame in the viral complementary sequence originates at nucleotide position 1827 and remains open for at least 71 amino acids (i.e., the extent of the second clone). A long stretch of hydrophobic amino acids is near the amino terminus of this predicted gene product. Between the two reading frames is a 60-nucleotide-long noncoding intergenic region. This nucleotide sequence can be arranged in hairpin configuration involving 14 G-C and 4 A-U base pairs. The possible function of this intergenic region in the regulation of transcription and/or translation is discussed.
两个重叠的DNA克隆代表了皮钦德沙粒病毒S RNA片段的一半以上,被克隆到pBR322中,并测定了它们的核苷酸序列。分析预测,病毒核衣壳蛋白(N)由病毒互补RNA序列中的一个阅读框编码,起始于病毒S RNA 3'端的核苷酸残基84,终止于1767 - 1769位的一个乳白密码子。终止密码子的位置已通过引物定向双脱氧核苷酸测序得到证实。N蛋白的计算大小为62,911 Da,净正电荷为 +9。在感染细胞提取物中已鉴定出指导N蛋白合成并与预测的N基因DNA杂交的病毒互补15 S mRNA。病毒互补序列中的第二个非重叠阅读框起始于核苷酸位置1827,并至少开放71个氨基酸(即第二个克隆的长度)。在这个预测的基因产物的氨基末端附近有一段很长的疏水氨基酸序列。在两个阅读框之间是一个60个核苷酸长的非编码基因间隔区。该核苷酸序列可以排列成涉及14个G - C和4个A - U碱基对的发夹结构。讨论了这个基因间隔区在转录和/或翻译调控中的可能功能。