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在编码干扰素诱导的色氨酰tRNA合成酶的mRNA合成中使用可变聚腺苷酸化位点。

Use of alternative polyadenylation sites in the synthesis of mRNAs encoding the interferon-induced tryptophanyl tRNA synthetase.

作者信息

Shen T, Anderson S L, Rubin B Y

机构信息

Department of Biological Sciences, Fordham University, Bronx, NY 10458, USA.

出版信息

Gene. 1996 Nov 14;179(2):225-9. doi: 10.1016/s0378-1119(96)00361-7.

Abstract

The interferon-mediated induction of the gene encoding the human tryptophanyl tRNA synthetase (WRS) results in the production of two mRNA species differing in size by approximately 800 base pairs (bp). Two distinctly sized cDNAs differing by approximately 800 bp were isolated from a cDNA library generated from mRNA prepared from IFN-gamma-treated cells. Northern blot analysis using cDNA probes recognizing different regions of the WRS mRNA reveals distinctly sized mRNAs differing in the length of their 3' untranslated regions. Differential display analysis using oligo dT primers demonstrates that the different sized WRS mRNAs result from alternative polyadenylation of this transcript.

摘要

干扰素介导的人类色氨酰-tRNA合成酶(WRS)编码基因的诱导导致产生两种大小相差约800个碱基对(bp)的mRNA种类。从由经干扰素-γ处理的细胞制备的mRNA构建的cDNA文库中分离出两种大小明显不同、相差约800 bp的cDNA。使用识别WRS mRNA不同区域的cDNA探针进行的Northern印迹分析显示,不同大小的mRNA在其3'非翻译区长度上存在差异。使用寡聚dT引物的差异显示分析表明,不同大小的WRS mRNA是该转录本可变聚腺苷酸化的结果。

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