Synthesis of mRNA by the parvovirus KRV in isolated nuclei.

Biken journal Pub Date : 1982-12-01
L A Salzman, P Fabisch, R Mitra, T Wali
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Abstract

We have synthesized vial-specific transcripts in nuclei isolated from cells infected with the parvovirus Kilham rat virus. Radioactive vial-specific RNA synthesized in the nuclei was extracted, hybridized to viral DNA, incubated in glyoxal, and electrophoresed in an agarose gel. At least five viral-specific RNAs were detected containing 4.6 Kb (25-26S), 3.2 Kb (major species, 20-22S), 2.9 Kb, 1.3 Kb, and 1.0 Kb pairs. The 4.6 Kb RNA represents a transcript of 95-100% of the viral genome. The major 3.2 and 2.9 Kb RNAs represent a transcript of 50-60% of the viral genome. Over 65% of the viral-specific RNA in the isolated nuclei is polyadenylylated on the 3' terminus. The 5' terminus of the RNA is capped in vitro by the sequence m7G(5')ppp(5')A. Incorporation of [beta-32p]ATP into the 5' cap sequence suggests that initiation of viral RNA synthesis may occur in the infected isolated nuclei.

微小病毒KRV在分离细胞核中合成mRNA。
我们已经在感染了克勒姆鼠细小病毒的细胞分离的细胞核中合成了小病毒特异性转录本。提取核中合成的放射性小瓶特异性RNA,与病毒DNA杂交,在乙二醛中孵育,并在琼脂糖凝胶中电泳。检测到至少5个病毒特异性rna,分别为4.6 Kb (25-26S)、3.2 Kb(主要物种,20-22S)、2.9 Kb、1.3 Kb和1.0 Kb对。4.6 Kb RNA代表了95-100%的病毒基因组转录本。主要的3.2 Kb和2.9 Kb rna代表了病毒基因组50-60%的转录本。在分离的细胞核中,超过65%的病毒特异性RNA在3'端被聚腺苷化。RNA的5'端在体外被序列m7G(5')ppp(5')A盖住。[β -32p]ATP与5'帽序列的结合表明,病毒RNA合成的起始可能发生在被感染的分离细胞核中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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