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PMID: 3108860 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Deletion analysis of a unique 3' splice site indicates that alternating guanine and thymine residues represent an efficient splicing signal.

Nucleic acids research ·Vol. 15 ·No. 9 ·1987-05-11 ·Pages 3787-99

Shelley CS, Baralle FE

Abstract

The 3' splice site of the second intron (I2) of the human apolipoprotein-AII gene, (GT)16GGGCAG, is unique in that, although fully functional, a stretch of alternating guanine and thymine residues replaces the polypyrimidine tract usually associated with 3' splice junctions. The transient expression of successive 5' deletion mutants has defined the minimum number of nucleotides at the 3' end of apo-AII I2 that are required to direct efficient splicing. Processing in two cell-types, representing apo-AII producing and non-producing tissue was identical; in both, only by removing all the GT repeats did the 3' splice site of apo-AII I2 become completely non-functional. Similar deletion analyses of "classic" 3' splice sites, which conform to the consensus sequence (Y)nNYAG, have indicated that a minimum of 14 nucleotides of the polypyrimidine tract are required for detectable levels of processing to take place. Here we report that the six nucleotides (GT)2GG, which directly replace this tract in a deletion mutant of the 3' splice site of apo-AII I2 are sufficient to direct the splicing process efficiently and correctly.

MeSH Terms
Apolipoprotein A-II Apolipoproteins A/genetics Base Sequence Chromosome Deletion Guanine/analysis Humans Introns RNA Splicing Thymidine/analysis
Chemicals
Apolipoprotein A-II Apolipoproteins A Guanine Thymidine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Shelley C S
Baralle F E
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37 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1987-05-11
Pages
3787-99
Language
English
Region
England
NLM ID
0411011
PMCID
PMC340782
Subset
IM
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