Müller H, Nitschke R
Med Microbiol Immunol. 1987;176(2):113-21. doi: 10.1007/BF00200683.
The molecular weights (mol. wts.) of the two double-stranded (ds) RNA segments of infectious bursal disease virus (IBDV) were determined using previously sequenced reovirus genes M3 and S2 as internal ds RNA reference molecules. Electrophoresis under fully denaturing conditions revealed mol. wts. of 2.26 X 10(6) daltons and 1.98 X 10(6) daltons. By direct length measurements under the electron microscope, using two different spreading conditions, the two segments were calculated to be composed of 3274 +/- 79 base pairs (bp) and 2821 +/- 59 bp or 3299 +/- 68 bp and 2830 +/- 73 bp, resulting in mol. wts. of 2.24-2.26 X 10(6) daltons and 1.93-1.94 X 10(6) daltons, respectively. Base pair distances of 2.67 +/- 0.08 A and 2.71 +/- 0.11 A in ds RNA were close to those of the A-RNA form; in ds DNA included as a control, the rise per base pair was 3.18 A, which is consistent with published results. Mol. wts. obtained for IBDV indicate that the RNAs of the other birnaviruses are also smaller than reported.
传染性法氏囊病病毒(IBDV)的两条双链(ds)RNA片段的分子量,是使用先前测序的呼肠孤病毒基因M3和S2作为内部ds RNA参考分子来测定的。在完全变性条件下进行电泳,得出分子量分别为2.26×10⁶道尔顿和1.98×10⁶道尔顿。通过在电子显微镜下采用两种不同的铺展条件进行直接长度测量,计算得出这两个片段分别由3274±79个碱基对(bp)和2821±59个bp或3299±68个bp和2830±73个bp组成,分子量分别为2.24 - 2.26×10⁶道尔顿和1.93 - 1.94×10⁶道尔顿。ds RNA中碱基对间距为2.67±0.08埃和2.71±0.11埃,接近A - RNA形式的间距;作为对照的ds DNA中,每个碱基对的上升高度为3.18埃,这与已发表的结果一致。IBDV的分子量表明,其他双RNA病毒科病毒的RNA也比报道的要小。