Rosel J, Moss B
J Virol. 1985 Dec;56(3):830-8. doi: 10.1128/JVI.56.3.830-838.1985.
We prepared antiserum that reacted with a major core polypeptide of approximately 62,000 daltons (62K polypeptide), designated 4b, and its 74K precursor, designated P4b. A cell-free translation product of vaccinia virus late mRNA that comigrated with P4b was specifically immunoprecipitated. The late mRNA encoding P4b hybridized to restriction fragments derived from the left end of the HindIII A fragment and to a lesser extent from the right side of the HindIII D fragment. A polypeptide that comigrated with P4a, the precursor of another major core polypeptide, was synthesized by mRNA that hybridized to DNA segments upstream of the P4b gene. Complete nucleotide sequence analysis of the P4b gene revealed an open reading frame, entirely within the HindIII A fragment, that was sufficient to encode a 644-amino-acid polypeptide of 73K. The 5' end of the P4b mRNA was located at or just above the translational initiation site.
我们制备了与一种约62,000道尔顿的主要核心多肽(62K多肽,命名为4b)及其74K前体(命名为P4b)发生反应的抗血清。与P4b迁移率相同的痘苗病毒晚期mRNA的无细胞翻译产物被特异性免疫沉淀。编码P4b的晚期mRNA与源自HindIII A片段左端的限制性片段杂交,与HindIII D片段右侧的杂交程度较低。与另一种主要核心多肽的前体P4a迁移率相同的一种多肽由与P4b基因上游DNA片段杂交的mRNA合成。P4b基因的完整核苷酸序列分析揭示了一个开放阅读框,完全位于HindIII A片段内,足以编码一个73K的644个氨基酸的多肽。P4b mRNA的5'端位于翻译起始位点或其上方。