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尽管近端序列元件(PSEs)之间相似度极低,但常见因子可通过胚胎海胆U1、U2和U6基因的近端序列元件指导转录。

Common factors direct transcription through the proximal sequence elements (PSEs) of the embryonic sea urchin U1, U2, and U6 genes despite minimal similarity among the PSEs.

作者信息

Li J M, Haberman R P, Marzluff W F

机构信息

Program in Molecular Biology and Biotechnology, University of North Carolina, Chapel Hill 27599, USA.

出版信息

Mol Cell Biol. 1996 Mar;16(3):1275-81. doi: 10.1128/MCB.16.3.1275.

Abstract

The proximal sequence element (PSE) for the sea urchin U6 small nuclear RNA gene has been defined. The most critical nucleotides for expression, located 61 to 64 nucleotides (nt) from the transcription start site, are 4 nt, AACT, at the 5' end of the PSE. Two nucleotide mutations in this region abolish transcription of the sea urchin U6 gene in vitro. The same two nucleotide mutations greatly reduce the binding of specific factors detected by an electrophoretic mobility shift assay. There is also a conserved AC dinucleotide 57 nt from the start site of the sea urchin U1 and U2 PSEs. The sea urchin U1 and U2 PSEs were substituted for the sea urchin U6 PSE, with the conserved AC sequences aligned with those of the U6 PSE. Both of these genes were expressed at levels higher than those observed with the wild-type U6 gene. Similar complexes are formed on the U1 and U2 PSEs, and formation of the complexes is inhibited efficiently by the U6 PSE. In addition, the E-box sequence present upstream of the PSE enhances U6 transcription from both the U1 and U2 PSEs. Finally, depletion of a nuclear extract with a DNA affinity column containing the U6 PSE sequence reduces expression of the U6 genes driven by the U6, U1, or U2 PSE but does not affect expression of the 5S rRNA gene. These data support the possibility that the same factor(s) interacts with the PSE sequences of the U1, U2, and U6 small nuclear RNA genes expressed in early sea urchin embryogenesis.

摘要

海胆U6小核RNA基因的近端序列元件(PSE)已被确定。对于表达最为关键的核苷酸,位于转录起始位点61至64个核苷酸(nt)处,是PSE 5'端的4个核苷酸AACT。该区域的两个核苷酸突变在体外消除了海胆U6基因的转录。同样的这两个核苷酸突变极大地降低了通过电泳迁移率变动分析检测到的特异性因子的结合。在海胆U1和U2 PSE起始位点57 nt处也有一个保守的AC二核苷酸。海胆U1和U2 PSE被替换为海胆U6 PSE,保守的AC序列与U6 PSE的那些序列对齐。这两个基因的表达水平均高于野生型U6基因所观察到的水平。在U1和U2 PSE上形成了类似的复合物,并且这些复合物的形成被U6 PSE有效抑制。此外,PSE上游存在的E盒序列增强了来自U1和U2 PSE的U6转录。最后,用含有U6 PSE序列的DNA亲和柱耗尽核提取物会降低由U6、U1或U2 PSE驱动的U6基因的表达,但不影响5S rRNA基因的表达。这些数据支持了在海胆早期胚胎发生中表达的U1、U2和U6小核RNA基因的PSE序列与相同因子相互作用的可能性。

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