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鞣酸促进多嘧啶序列结合蛋白的表达,并减轻先天性肌无力综合征中由于hnRNP H破坏突变导致的CHRNA1外显子P3A的有害内含。

Tannic acid facilitates expression of the polypyrimidine tract binding protein and alleviates deleterious inclusion of CHRNA1 exon P3A due to an hnRNP H-disrupting mutation in congenital myasthenic syndrome.

作者信息

Bian Yang, Masuda Akio, Matsuura Tohru, Ito Mikako, Okushin Kazuya, Engel Andrew G, Ohno Kinji

机构信息

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

Hum Mol Genet. 2009 Apr 1;18(7):1229-37. doi: 10.1093/hmg/ddp023. Epub 2009 Jan 15.

Abstract

We recently reported that the intronic splice-site mutation IVS3-8G>A of CHRNA1 that encodes the muscle nicotinic acetylcholine receptor alpha subunit disrupts binding of a splicing repressor, hnRNP H. This, in turn, results in exclusive inclusion of the downstream exon P3A. The P3A(+) transcript encodes a non-functional alpha subunit that comprises 50% of the transcripts in normal human skeletal muscle, but its functional significance remains undetermined. In an effort to search for a potential therapy, we screened off-label effects of 960 bioactive chemical compounds and found that tannic acid ameliorates the aberrant splicing due to IVS3-8G>A but without altering the expression of hnRNP H. Therefore, we searched for another splicing trans-factor. We found that the polypyrimidine tract binding protein (PTB) binds close to the 3' end of CHRNA1 intron 3, that PTB induces skipping of exon P3A and that tannic acid increases the expression of PTB in a dose-dependent manner. Deletion assays of the PTB promoter region revealed that the tannic acid-responsive element is between positions -232 and -74 from the translation initiation site. These observations open the door to the discovery of novel therapies based on PTB overexpression and to detecting possible untoward effects of the overexpression.

摘要

我们最近报道,编码肌肉烟碱型乙酰胆碱受体α亚基的CHRNA1基因内含子剪接位点突变IVS3-8G>A破坏了剪接阻遏物hnRNP H的结合。这进而导致下游外显子P3A的选择性包含。P3A(+)转录本编码一种无功能的α亚基,其在正常人类骨骼肌转录本中占50%,但其功能意义仍未确定。为了寻找潜在的治疗方法,我们筛选了960种生物活性化合物的非标签效应,发现单宁酸可改善由IVS3-8G>A导致的异常剪接,但不改变hnRNP H的表达。因此,我们寻找另一种剪接反式因子。我们发现多嘧啶序列结合蛋白(PTB)结合在CHRNA1基因内含子3的3'端附近,PTB诱导外显子P3A跳跃,且单宁酸以剂量依赖的方式增加PTB的表达。PTB启动子区域的缺失分析表明,单宁酸反应元件位于翻译起始位点上游-232至-74位之间。这些观察结果为基于PTB过表达发现新疗法以及检测过表达可能产生的不良影响打开了大门。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afeb/2655771/080815107f08/ddp02301.jpg

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