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Non-random localization of ribonucleoprotein (RNP) structures within an adenovirus mRNA precursor

机译:腺病毒mRNA前体内的核糖核蛋白(RNP)结构的非随机定位

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Heterogeneous nuclear protein complexes (hnRNP) containing the precursor RNA from the adenovirus early region 2 were analysed to determine the specificity of protein-RNA interaction. RNA precursor sequences were present in isolated hnRNP complexes and endogenous 30S particles. At least 20–40 bases long fragments were protected when RNase A was used to remove unprotected RNA sequences in hnRNA complexes. Similarly around 40 bases of RNA were protected in 30S particles. These sequences represent discrete regions of the adenovirus genome. Especially sequences complementary to the EcoRI-F fragment encoding the first leader and the major intron for the DNA binding protein (DBP) RNA precursor, were analysed in detail. Tentatively, sequences resistant to RNase A were located in the middle of the intron and at the splicedonor junction of the first leader of the DBP precursor RNA. The same sequences were identified irrespective whether hnRNP complexes or 30S particles were used suggesting that 30S particles originate from hnRNP complexes. A 38.000 dalton protein appears to be in direct contact with RNA sequences complementary to the EcoRI-F fragment.
机译:分析含有来自腺病毒早期区域2的前体RNA的异质核蛋白质复合物(HNRNP)以确定蛋白质RNA相互作用的特异性。在分离的HNRNP络合物中存在RNA前体序列和内源30S颗粒。当RNase A用于去除HNRNA复合物中的未受保护的RNA序列时,保护至少20-40个基质长片段。类似地,在30S颗粒中类似地保护40个RNA。这些序列代表腺病毒基因组的离散区域。特别详细地分析了对编码第一领导者的ECORI-F片段的序列和用于DNA结合蛋白(DBP)RNA前体的主要内含子进行互补的序列。暂时,对RNase A抵抗的序列位于内含子中的中间,并在DBP前体RNA的第一个领导者的Splicedonor结处。无论使用HNRNP复合物还是30S颗粒都被使用表明30S颗粒源自HNRNP络合物,鉴定了相同的序列。 38.000 dalton蛋白质似乎与与EcoRI-F片段互补的RNA序列直接接触。

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