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首页> 外文期刊>FEBS Letters >Point mutations within 663–666 bp of intron 6 of the human TDO2 gene, associated with a number of psychiatric disorders, damage the YY‐1 transcription factor binding site
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Point mutations within 663–666 bp of intron 6 of the human TDO2 gene, associated with a number of psychiatric disorders, damage the YY‐1 transcription factor binding site

机译:人类TDO2基因内含子6的663–666 bp范围内的点突变,与许多精神疾病有关,破坏了YY-1转录因子结合位点

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摘要

>Single base mutations G→A at position 663 and G→T at position 666 of intron 6 of the human tryptophan oxygenase gene (TDO2) are associated with a variety of psychiatric disorders [Comings, D.E. et al. (1996) Pharmacogenetics 6, 307–318]. Binding of rat liver nuclear extract proteins to synthetic double-strand oligonucleotides corresponding to three allelic states of the region between 651 bp and 680 bp of human TDO2 intron 6 has been studied by gel shift assay. It has been demonstrated that to each allelic state of the region there corresponds a specific set of proteins that interacts with it. With the aid of computer analysis and using specific anti-YY-1 antibodies it has been shown that both mutations damage the YY-1 transcription factor binding site.
机译:>人色氨酸加氧酶基因( TDO2 )内含子6的663位单碱基突变G→A和666的G→T突变与多种精神病有关[Comings,D.E.等。 (1996)Pharmacogenetics 6,307-318]。通过凝胶位移分析研究了大鼠肝核提取物蛋白与合成的双链寡核苷酸的结合,该寡核苷酸对应于人类 TDO2 内含子6的651 bp和680 bp之间区域的三个等位基因状态。已经证明,对于该区域的每个等位基因状态,存在与之相互作用的一组特定的蛋白质。借助于计算机分析并使用特异性的抗YY-1抗体,已显示两种突变均破坏YY-1转录因子结合位点。

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