PARTIAL DELETION OF A DYSTROPHIN GENE LEADS TO EXON SKIPPING AND TO LOSS OF AN INTRA-EXON HAIRPIN STRUCTURE FROM THE PREDICTED MESSENGER-RNA PRECURSOR

被引:20
作者
MATSUO, M
NISHIO, H
KITOH, Y
FRANCKE, U
NAKAMURA, H
机构
[1] KOBE UNIV,SCH MED,DEPT PEDIAT,KOBE 650,JAPAN
[2] STANFORD UNIV,MED CTR,HOWARD HUGHES MED INST,STANFORD,CA 94305
[3] STANFORD UNIV,MED CTR,DEPT GENET & PEDIAT,STANFORD,CA 94305
关键词
D O I
10.1016/0006-291X(92)91759-J
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In dystrophin Kobe exon 19 of the dystrophin gene is skipped during the process of mRNA precursor splicing even though the splice sites are unchanged (Matsuo et al. J. Clin. Invest. 87:2127-2131, 1991). In the predicted secondary structure of the mRNA precursor, exon 19 of dystrophin Kobe is paired with intron sequences, whereas a large part of exon sequence from wild type is paired with itself and folded into a large hairpin structure. As all of 22 additional dystrophin exons analyzed also form intra-exon hairpin structures, these structures may be considered essential components of exons. We suggest that the abolishment of a hairpin structure in the truncated exon of dystrophin Kobe might prevent the splicing machinery from recognizing the splice sites and induce exon skipping. © 1992.
引用
收藏
页码:495 / 500
页数:6
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