2008
DOI: 10.1007/978-3-540-76776-3_3
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Splice Site Requirements and Switches in Plants

Abstract: Intron sequences in nuclear pre-mRNAs are excised with either the major U2 snRNA-dependent spliceosomal pathway or the minor U12 snRNAdependent spliceosomal pathway that exist in most eukaryotic organisms. While the predominant dinucleotides bordering each of these types of introns and the catalytic mechanism used in their excision are conserved in plants and animals, several features aiding in the recognition of plant introns are distinct from those in animals and yeast. Along with their short length, high AU… Show more

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Cited by 29 publications
(30 citation statements)
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“…A normal ESP transcript, and hence the 238 bp amplicon, is generated by splicing the unique ESP intron at a canonical 5 0 splice site AG-GT (exon-intron) for Mt-0 and a non-canonical AG-AT 5 0 splice site for Col-0 (Barbazuk et al 2008;Reddy 2007). Although the GT to AT mutation of the 5 0 splice site we observed for ESP in Col-0 seems to be a rather rare event, it has been reported for other plant genes leading to diverse effects including intron retention and consequently premature translation termination (Schuler 2008). The 350 bp amplicon in Col-0 is generated by the use of a distal 5 0 splice site with a CG-GT sequence and situated 110 bp downstream into the intron ( Fig.…”
Section: Characterisation Of An Alternative Splicing Event For Espmentioning
confidence: 41%
“…A normal ESP transcript, and hence the 238 bp amplicon, is generated by splicing the unique ESP intron at a canonical 5 0 splice site AG-GT (exon-intron) for Mt-0 and a non-canonical AG-AT 5 0 splice site for Col-0 (Barbazuk et al 2008;Reddy 2007). Although the GT to AT mutation of the 5 0 splice site we observed for ESP in Col-0 seems to be a rather rare event, it has been reported for other plant genes leading to diverse effects including intron retention and consequently premature translation termination (Schuler 2008). The 350 bp amplicon in Col-0 is generated by the use of a distal 5 0 splice site with a CG-GT sequence and situated 110 bp downstream into the intron ( Fig.…”
Section: Characterisation Of An Alternative Splicing Event For Espmentioning
confidence: 41%
“…2A), with the only discernible difference being localized to the cleavage site. This difference probably reflects the marked tendency of plant introns to be U-rich (20,21) and thus to have a lower C content than would be seen near a "normal" poly(A) site. Other than this, the base composition profiles of 3′-UTR (as in Fig.…”
Section: Resultsmentioning
confidence: 94%
“…Similar to other eukaryotes, plant pre-mRNA splicing is a nuclear process that involves the recognition of exon–intron junctions by the spliceosome (Brown and Simpson, 1998; Maquat, 2004; Reddy, 2007; Schuler, 2008). The spliceosome is assembled from small nuclear RNAs (snRNAs) and associated proteins that make up the small nuclear ribonucleoprotein particles (snRNPs) that recognize and splice introns.…”
Section: Resultsmentioning
confidence: 99%