Duggal R, Hall T C
Institute of Developmental and Molecular Biology, Texas A&M University, College Station 77843-3155, USA.
Virology. 1995 Dec 20;214(2):638-41. doi: 10.1006/viro.1995.0077.
The binding of five barley proteins (Mr: 37, 36, 35, 34, and 30 kDa) to the ICR2 motif present at the 5' end of brome mosaic virus (BMV) RNA-2 was identified using UV cross-linking. Evidence that the interaction is specific included the observation that these proteins did not recognize a similar-size RNA fragment transcribed from a nonviral (beta-glucuronidase) gene, nor did they bind to the 3' end of the plus strand of RNA-3. Replication-defective BMV RNA-2 mutants bearing substitution mutations at nucleotides 9 and 10 of the ICR2 motif were used to show that these positions were involved in the interaction of the five barley proteins with BMV RNA-2. Surprisingly, the profile of barley proteins interacting with the 3' end of the minus strand of RNA-2 was similar to that seen for the 5' end of the plus strand. Further, the profile of proteins binding to minus-sense probes bearing substitution mutations in the ICR2 region differed from that found for the wild-type sequence. These findings support the concept that host proteins are involved in genome replication and that their ability to interact with both plus and minus strands of the viral RNA is probably involved with the initiation of plus-strand synthesis.
利用紫外线交联技术鉴定了五种大麦蛋白(分子量分别为37、36、35、34和30 kDa)与雀麦花叶病毒(BMV)RNA - 2 5'端存在的ICR2基序的结合。这种相互作用具有特异性的证据包括:观察到这些蛋白不识别从非病毒(β - 葡萄糖醛酸酶)基因转录的类似大小的RNA片段,也不与RNA - 3正链的3'端结合。携带ICR2基序核苷酸9和10处替代突变的复制缺陷型BMV RNA - 2突变体被用于表明这些位置参与了五种大麦蛋白与BMV RNA - 2的相互作用。令人惊讶的是,与RNA - 2负链3'端相互作用的大麦蛋白谱与正链5'端的相似。此外,与ICR2区域带有替代突变的负义探针结合的蛋白谱与野生型序列不同。这些发现支持了宿主蛋白参与基因组复制的概念,并且它们与病毒RNA正负链相互作用的能力可能与正链合成的起始有关。