Skinner M A, Siddell S G
J Gen Virol. 1985 Mar;66 ( Pt 3):593-6. doi: 10.1099/0022-1317-66-3-593.
A coding sequence at the 5' end of mRNA 4 of the coronavirus MHV-JHM was determined by M13/chain-terminator sequencing of cloned cDNA. An open reading frame of 417 bases with the potential to encode a polypeptide of mol. wt. 15 200 (139 residues) was identified. The 3' end of the open reading frame overlapped by 16 bases the start of an open reading frame found in mRNA 5. The translation product of mRNA 4 was predicted to be a basic polypeptide rich in threonine. It had a large hydrophobic region near the amino terminus and a basic carboxy terminus. An intracellular, virus-specific polypeptide, which has been previously described having a mol. wt. of 14 000 to 14 500 has the size and charge characteristics of such a translation product.
通过对克隆的cDNA进行M13/链终止测序,确定了冠状病毒MHV-JHM的mRNA 4 5'端的编码序列。鉴定出一个417个碱基的开放阅读框,它有可能编码一个分子量为15200(139个残基)的多肽。该开放阅读框的3'端与mRNA 5中发现的一个开放阅读框的起始部分重叠16个碱基。预计mRNA 4的翻译产物是一种富含苏氨酸的碱性多肽。它在氨基末端附近有一个大的疏水区域和一个碱性的羧基末端。先前已描述过一种分子量为14000至14500的细胞内病毒特异性多肽,具有这种翻译产物的大小和电荷特征。