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Molecular and Cellular Biology, September 2000, p. 6414-6425, Vol. 20, No. 17
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Multiple Splicing Defects in an Intronic
False Exon
Hanzhen
Sun and
Lawrence A.
Chasin*
Department of Biological Sciences, Columbia
University, New York, New York 10027
Received 25 February 2000/Returned for modification 17 April
2000/Accepted 15 June 2000
Splice site consensus sequences alone are insufficient to dictate
the recognition of real constitutive splice sites within the typically
large transcripts of higher eukaryotes, and large numbers of
pseudoexons flanked by pseudosplice sites with good matches to the
consensus sequences can be easily designated. In an attempt to identify
elements that prevent pseudoexon splicing, we have systematically
altered known splicing signals, as well as immediately adjacent
flanking sequences, of an arbitrarily chosen pseudoexon from intron 1 of the human hprt gene. The substitution of a 5' splice
site that perfectly matches the 5' consensus combined with mutation to
match the CAG/G sequence of the 3' consensus failed to get this model
pseudoexon included as the central exon in a dhfr minigene
context. Provision of a real 3' splice site and a consensus 5' splice
site and removal of an upstream inhibitory sequence were necessary and
sufficient to confer splicing on the pseudoexon. This activated context
also supported the splicing of a second pseudoexon sequence containing
no apparent enhancer. Thus, both the 5' splice site sequence and the
polypyrimidine tract of the pseudoexon are defective despite their good
agreement with the consensus. On the other hand, the pseudoexon body
did not exert a negative influence on splicing. The introduction into the pseudoexon of a sequence selected for binding to ASF/SF2 or its
replacement with
-globin exon 2 only partially reversed the effect
of the upstream negative element and the defective polypyrimidine tract. These results support the idea that exon-bridging enhancers are
not a prerequisite for constitutive exon definition and suggest that
intrinsically defective splice sites and negative elements play
important roles in distinguishing the real splicing signal from the
vast number of false splicing signals.
*
Corresponding author. Mailing address: 912 Fairchild,
Department of Biological Sciences, Columbia University, New York, NY 10027. Phone: (212) 854-4645. Fax: (212) 531-0425. E-mail:
lac2{at}columbia.edu.
Molecular and Cellular Biology, September 2000, p. 6414-6425, Vol. 20, No. 17
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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