Nagata L, Masri S A, Mah D C, Lee P W
Nucleic Acids Res. 1984 Nov 26;12(22):8699-710. doi: 10.1093/nar/12.22.8699.
The complete sequence of the reovirus (serotype 3) S1 gene was obtained by using cloned cDNA derived from the RNA segment. This gene is 1416 nucleotides in length and contains two open reading frames. The first reading frame has a coding capacity of 455 amino acids, sufficient to account for the known S1 product, protein sigma 1 (42,000 MW). It possesses a signal peptide as well as three possible glycosylation sites. No homology could be detected when this gene sequence and the deduced amino acid sequence were compared to published sequences of the corresponding gene of a human rotavirus. The second reading frame (not in phase with the first) starts at the second ATG recently shown to be a functional initiation site. It has a coding capacity of 120 amino acids. Its outstanding feature is the highly basic amino-terminal region, a characteristic apparently shared by a number of DNA binding proteins. It is speculated that this protein, hitherto undetected, may play a role in mediating viral and/or host nucleic acid transcription.
通过使用源自RNA片段的克隆cDNA,获得了呼肠孤病毒(3型)S1基因的完整序列。该基因长度为1416个核苷酸,包含两个开放阅读框。第一个阅读框编码能力为455个氨基酸,足以解释已知的S1产物,即σ1蛋白(42,000 MW)。它具有一个信号肽以及三个可能的糖基化位点。当将该基因序列和推导的氨基酸序列与人类轮状病毒相应基因的已发表序列进行比较时,未检测到同源性。第二个阅读框(与第一个不同相)从最近显示为功能性起始位点的第二个ATG开始。它的编码能力为120个氨基酸。其突出特点是高度碱性的氨基末端区域,这一特征显然为许多DNA结合蛋白所共有。据推测,这种迄今未被检测到的蛋白可能在介导病毒和/或宿主核酸转录中发挥作用。