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一个双向剪接调节元件通过协调异质性核糖核蛋白A1的协同结合来调节HIV-1反式激活因子(tat)和调节/病毒蛋白表达因子(rev)的mRNA产生。

A Janus splicing regulatory element modulates HIV-1 tat and rev mRNA production by coordination of hnRNP A1 cooperative binding.

作者信息

Marchand Virginie, Méreau Agnès, Jacquenet Sandrine, Thomas Denise, Mougin Annie, Gattoni Renata, Stévenin James, Branlant Christiane

机构信息

Laboratoire de Maturation des ARN et Enzymologie Moléculaire, UMR 7567 UHP-CNRS, Université Henri Poincaré Nancy 1, Boulevard des Aiguillettes, BP239, 54506 Cedex, Vandoeuvre-lès-Nancy, France.

出版信息

J Mol Biol. 2002 Nov 1;323(4):629-52. doi: 10.1016/s0022-2836(02)00967-1.

Abstract

Retroviral protein production depends upon alternative splicing of the viral transcript. The HIV-1 acceptor site A7 is required for tat and rev mRNA production. Production of the Tat transcriptional activator is highly controlled because of its apoptotic properties. Two silencer elements (ESS3 and ISS) and two enhancer elements (ESE2 and ESE3/(GAA)3) were previously identified at site A7. hnRNP A1 binds ISS and ESS3 and is involved in the inhibitory process, ASF/SF2 activates site A7 utilisation. Here, by using chemical and enzymatic probes we established the 2D structure of the HIV-1(BRU) RNA region containing site A7 and identified the RNA segments protected in nuclear extract and by purified hnRNP A1. ISS, ESE3/(GAA)3 and ESS3 are located in three distinct stem-loop structures (SLS1, 2 and 3). As expected, hnRNP A1 binds sites 1, 2 and 3 of ISS and ESS3b, and oligomerises on the polypurine sequence upstream of ESS3b. In addition, we discovered an unidentified hnRNP A1 binding site (AUAGAA), that overlaps ESE3/(GAA)3. On the basis of competition experiments, hnRNP A1 has a stronger affinity for this site than for ESS3b. By insertion of (GAA)3 alone or preceded by the AUA trinucleotide in a foreign context, the AUAGAA sequence was found to modulate strongly the (GAA)3 splicing enhancer activity. Cross-linking experiments on these heterologous RNAs and the SLS2-SLS3 HIV-1 RNA region, in nuclear extract and with recombinant proteins, showed that binding of hnRNP A1 to AUA(GAA)3 strongly competes the association of ASF/SF2 with (GAA)3. In addition, disruption of AUA(GAA)3 demonstrated a key role of this sequence in hnRNP A1 cooperative binding to the ISS and ESS3b inhibitors and hnRNP A1 oligomerisation on the polypurine sequence. Thus, depending on the cellular context ([ASF/SF2]/[hnRNP A1] ratio), AUA(GAA)3 will activate or repress site A7 utilisation and can thus be considered as a Janus splicing regulator.

摘要

逆转录病毒蛋白的产生依赖于病毒转录本的可变剪接。HIV-1的A7受体位点是tat和rev mRNA产生所必需的。由于Tat转录激活因子具有凋亡特性,其产生受到高度调控。先前在A7位点鉴定出两个沉默元件(ESS3和ISS)和两个增强子元件(ESE2和ESE3/(GAA)3)。hnRNP A1结合ISS和ESS3并参与抑制过程,ASF/SF2激活A7位点的利用。在此,通过使用化学和酶促探针,我们确定了包含A7位点的HIV-1(BRU) RNA区域的二维结构,并鉴定了在核提取物和纯化的hnRNP A1中受到保护的RNA片段。ISS、ESE3/(GAA)3和ESS3位于三个不同的茎环结构(SLS1、2和3)中。正如预期的那样,hnRNP A1结合ISS和ESS3b的位点1、2和3,并在ESS3b上游的多聚嘌呤序列上寡聚化。此外,我们发现了一个未鉴定的hnRNP A1结合位点(AUAGAA),它与ESE3/(GAA)3重叠。基于竞争实验,hnRNP A1对该位点的亲和力比对ESS3b的亲和力更强。通过在异源背景下单独插入(GAA)3或在其前面插入AUA三核苷酸,发现AUAGAA序列强烈调节(GAA)3剪接增强子活性。在核提取物中以及与重组蛋白一起对这些异源RNA和SLS2-SLS3 HIV-1 RNA区域进行交联实验表明,hnRNP A1与AUA(GAA)3的结合强烈竞争ASF/SF2与(GAA)3的结合。此外,破坏AUA(GAA)3证明了该序列在hnRNP A1与ISS和ESS3b抑制剂的协同结合以及hnRNP A1在多聚嘌呤序列上的寡聚化中的关键作用。因此,根据细胞环境([ASF/SF2]/[hnRNP A1]比值),AUA(GAA)3将激活或抑制A7位点的利用,因此可被视为一种双面剪接调节因子。

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