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人类CD59的基因结构以及通过可变聚腺苷酸化产生离散mRNA的证明。

Gene structure of human CD59 and demonstration that discrete mRNAs are generated by alternative polyadenylation.

作者信息

Tone M, Walsh L A, Waldmann H

机构信息

Department of Pathology, University of Cambridge, U.K.

出版信息

J Mol Biol. 1992 Oct 5;227(3):971-6. doi: 10.1016/0022-2836(92)90239-g.

Abstract

We have isolated the CD59 gene from human genomic libraries. The gene is distributed over more than 27 x 10(3) base-pairs and consists of one 5'-untranslated exon and three coding exons. The gene structure is similar to that of mouse Ly-6 with the exception of the larger size of CD59 introns. Northern blot analysis using six different probes located in the 3'-region of the gene shows that more than four different CD59 mRNA molecules are generated by alternative polyadenylation. Three of these polyadenylation sites were predicted from previously published cDNA sequences. We have isolated a fourth from Jurkat poly(A)+ RNA by the procedure of rapid amplification of cDNA ends. Alternative polyadenylation may be due to the RNA secondary structure around the typical polyadenylation signal, AAUAAA.

摘要

我们已从人类基因组文库中分离出CD59基因。该基因分布在超过27×10³个碱基对中,由一个5'非翻译外显子和三个编码外显子组成。除了CD59内含子较大外,该基因结构与小鼠Ly-6相似。使用位于该基因3'区域的六种不同探针进行的Northern印迹分析表明,通过可变聚腺苷酸化产生了四种以上不同的CD59 mRNA分子。其中三个聚腺苷酸化位点是根据先前发表的cDNA序列预测的。我们通过cDNA末端快速扩增程序从Jurkat poly(A)+ RNA中分离出了第四个位点。可变聚腺苷酸化可能是由于典型聚腺苷酸化信号AAUAAA周围的RNA二级结构所致。

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