RNABiochemistryPeer-reviewed journal article
Extremely fast and incredibly close: co-transcriptional splicing in budding yeast
Abstract
RNA splicing, an essential part of eukaryotic pre-messenger RNA processing, can be simultaneous with transcription by RNA polymerase II. Here, we compare and review independent next-generation sequencing methods that quantify co-transcriptional splicing in budding yeast. Splicing in yeast is fast, taking place within seconds of intron transcription, while polymerase is within a few dozens of nucleotides of the 3 splice site. Ribosomal protein mRNAs are spliced particularly fast and co-transcriptionally. Intron-mediated regulation of some genes is also likely to be co-transcriptional. We suggest that intermediates of the splicing reaction, missing from current datasets, may hold key information about splicing kinetics.\n\nTrendsO_LIIndependent next-generation sequencing methods quantify co-transcriptional splicing in budding yeast\nC_LIO_LIRibosomal protein mRNAs are spliced particularly fast and co-transcriptionally\nC_LIO_LIIntron-mediated regulation of DBP2 and RPS9A is likely co-transcriptional\nC_LIO_LISplicing intermediates, missing from current datasets, may hold key information\nC_LI
- organism: yeast
- assay: DNA methylation
- research focus: chromatin & epigenetic regulation
- approach: experimental assay
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