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Sequences at the capped 5-ends of polyoma virus late region mRNAs: an example of extreme terminal heterogeneity.

机译:多瘤病毒晚期区域mRNA的带帽5端序列:极端末端异质性的一个例子。

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摘要

We have localized with respect to the genomic DNA sequence the capped 5'-termini of polyoma virus late region mRNAs. A minimum of fifteen different purine termini were found within a 94 base pair region (66.36 to 68.12 map units, nt 5075-5168) immediately preceding the sequence determining the late region mRNA leader repeat (1-3). The most common termini occur at nearly every possible purine within a 25 bp sequence proximal to the leader repeat unit. These do not bear the usual positional relationship to a sequence resembling the 'TATA' box consensus. Deletion mutants lacking minor cap sites and sequences upstream from the principal cap sites were viable. A deletion mutant lacking one of the principal cap sites formed small plaques, while a slightly larger deletion further impinging on the principal cap site region was non-viable. The principal cap sites, which we assume to be transcriptional initiation points, are included in a DNaseI hypersensitive region of polyoma virus chromatin (4).
机译:关于基因组DNA序列,我们已经定位了多瘤病毒晚期区域mRNA的5'端的加帽。在确定晚期区域mRNA前导序列重复序列(1-3)之前的94个碱基对区域(66.36至68.12个图单元,nt 5075-5168)中发现了至少十五个不同的嘌呤末端。最常见的末端出现在前导重复单元近端25 bp序列内几乎所有可能的嘌呤中。它们与类似于“ TATA”框共有序列的序列没有通常的位置关系。缺失突变体缺少较小的帽状位点,并且在主要帽状位点上游的序列是可行的。缺少主要帽状位点之一的缺失突变体形成小斑块,而进一步撞击在主要帽状位点区域上的稍大的缺失是不可行的。我们假设是转录起始点的主要帽位点包含在多瘤病毒染色质的DNaseI超敏区中(4)。

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