CALCITONIN EXON SEQUENCES INFLUENCE ALTERNATIVE RNA PROCESSING

被引:19
作者
COTE, GJ
NGUYEN, IN
BERGET, SM
GAGEL, RF
机构
[1] VET ADM MED CTR,DEPT MED,MOLEC & CELLULAR ENDOCRINOL LAB,111E,2002 HOLCOMBE BLVD,HOUSTON,TX 77030
[2] VET ADM MED CTR,DEPT BIOCHEM,HOUSTON,TX 77030
[3] BAYLOR UNIV,HOUSTON,TX 77030
关键词
D O I
10.1210/mend-4-11-1744
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The pre-mRNA encoding calcitonin (CT) and CT gene-related peptide (CGRP) is differentially processed in a tissue-specific fashion to include exon 4 (which encodes CT) or exclude this exon and splice to exon 5 (which encodes CGRP). We have used a CT-specific in vitro RNA-processing system to identify cis-acting sequences required to prevent splicing to exon 5. Deletion mapping demonstrated the presence of an element within the first 45 nucleotides of the CT-specific exon 4 that was required to suppress splicing to the CGRP-specific exon 5. This element was able to function in a completely heterologous system to suppress splicing when the CGRP exon was replaced with a constitutive viral exon. The element was unable to suppress splicing in the absence of a proximal CT-specific 3' splice site. Our results suggest that CT-specific splicing requires assisted recognition of its 3' splice site. © 1990 by The Endocrine Society.
引用
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页码:1744 / 1749
页数:6
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