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囊性纤维化跨膜传导调节因子mRNA中可变外显子9跳跃的遗传基础。

Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA.

作者信息

Chu C S, Trapnell B C, Curristin S, Cutting G R, Crystal R G

机构信息

Pulmonary Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Nat Genet. 1993 Feb;3(2):151-6. doi: 10.1038/ng0293-151.

Abstract

Variable in-frame skipping of exon 9 in cystic fibrosis transmembrane conductance regulator (CFTR) mRNA transcripts (exon 9-) occurs in the respiratory epithelium. To explore the genetic basis of this event, we evaluated respiratory epithelial cells and blood leukocytes from 124 individuals (38 with cystic fibrosis (CF), 86 without CF). We found an inverse relationship between the length of the polythymidine tract at the exon 9 splice branch/acceptor site and the proportion of exon 9- CFTR mRNA transcripts. These results strongly indicate a genetic basis in vivo modulating post-transcriptional processing of CFTR mRNA transcripts.

摘要

囊性纤维化跨膜传导调节因子(CFTR)mRNA转录本中外显子9的可变框内跳跃(外显子9-)发生于呼吸道上皮细胞。为探究这一现象的遗传基础,我们评估了124名个体(38名患有囊性纤维化(CF),86名未患CF)的呼吸道上皮细胞和血液白细胞。我们发现外显子9剪接分支/受体位点处多聚胸腺嘧啶序列的长度与外显子9-CFTR mRNA转录本的比例呈负相关。这些结果有力地表明了体内存在调节CFTR mRNA转录本转录后加工的遗传基础。

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