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非洲爪蟾核糖体RNA转录起始和终止位点的核苷酸序列。

The nucleotide sequence of the initiation and termination sites for ribosomal RNA transcription in X. laevis.

作者信息

Sollner-Webb B, Reeder R H

出版信息

Cell. 1979 Oct;18(2):485-99. doi: 10.1016/0092-8674(79)90066-7.

Abstract

In this study, we have located the sites of transcription initiation and termination on a cloned fragment of ribosomal DNA from X. laevis, and have sequenced the surrounding nucleotides. As reported previously (Reeder, Sollner-Webb and Wahn, 1977), about 25% of the 40S rRNA precursor molecules isolated from oocytes have polyphosphate 5' termini and are therefore presumed to represent primary transcripts. These ends hybridize specifically to the 221 bp DNA fragment and removed the overhanging DNA region with S1 nuclease. In the other, we hybridized 40S RNA to a 221 bp fragment of ribosomal DNA. The nucleotides encoding the 5' end of the 40S RNA were located more precisely by two methods. In one, we hybridized 40S RNA to the 221 bp DNA fragment and removed the overhanging DNA region with S1 nuclease. In the other, we hybridized 40S RNA to a smaller DNA fragment and extended the recessed 3' terminus of the DNA using reverse transcriptase. The resultant DNA fragments were sized on sequencing gels. Both determinations map the 5' end of 40S RNA at the same site in the rDNA, about 2250 bp upstream from the Eco RI site in the 18S rRNA coding sequence. At this site we find a DNA sequence beginning AGGGGAAGAC.... which agrees with partial sequence data from the 5' end of polyphosphorylated and bulk 40S rRNA. Features of this region of the ribosomal DNA will be discussed in this paper. A 227 nucleotide region surrounding the initiation site was also sequenced from an independently derived clone and found to differ in only one nucleotide. In addition, a sequence is found about 1100 nucleotides upstream from the 5' end of the gene that has 90% homology to the sequence from nucleotides minus 125 to +4 in the initiation region. At the termination region, X. laevis ribosomal DNA has a single recognition site for the restriction enzyme Hind III in each repeating unit. Using the S1 nuclease technique, the 3' termini of both the 40S precursor and mature 28S rRNA are seen to map within this recognition sequence. The sequence surrounding the Hind III site has striking homology to termination sites recognized by other RNA polymerase classes. Sequences with similar features are also found upstream from the initiation site.

摘要

在本研究中,我们已确定了非洲爪蟾核糖体DNA克隆片段上转录起始和终止的位点,并对周围的核苷酸进行了测序。如先前报道(里德、索尔纳 - 韦伯和瓦恩,1977年),从卵母细胞中分离出的40S rRNA前体分子中约25%具有多磷酸5'末端,因此被认为代表初级转录本。这些末端与221 bp的DNA片段特异性杂交,并用S1核酸酶去除突出的DNA区域。在另一种方法中,我们将40S RNA与核糖体DNA的221 bp片段杂交。通过两种方法更精确地定位了编码40S RNA 5'末端的核苷酸。一种方法是,我们将40S RNA与221 bp的DNA片段杂交,并用S1核酸酶去除突出的DNA区域。另一种方法是,我们将40S RNA与一个较小的DNA片段杂交,并用逆转录酶延伸DNA凹陷的3'末端。所得的DNA片段在测序凝胶上进行大小测定。两种测定方法都将40S RNA的5'末端定位在rDNA中的同一位点,位于18S rRNA编码序列中Eco RI位点上游约2250 bp处。在这个位点,我们发现一个以AGGGGAAGAC……开头的DNA序列,这与多磷酸化和大量40S rRNA 5'末端的部分序列数据一致。本文将讨论核糖体DNA这一区域的特征。围绕起始位点的一个227核苷酸区域也从一个独立衍生的克隆中进行了测序,发现仅在一个核苷酸上有所不同。此外,在基因5'末端上游约1100个核苷酸处发现了一个序列,它与起始区域中从核苷酸 - 125到 +4的序列具有90%的同源性。在终止区域,非洲爪蟾核糖体DNA在每个重复单元中对限制性内切酶Hind III有一个单一的识别位点。使用S1核酸酶技术,可以看到40S前体和成熟28S rRNA的3'末端都定位在这个识别序列内。Hind III位点周围的序列与其他RNA聚合酶类识别的终止位点具有显著的同源性。在起始位点上游也发现了具有类似特征的序列。

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