Show simple item record

dc.contributor.authorPai, Athma A
dc.contributor.authorPaggi, Joseph
dc.contributor.authorAdelman, Karen
dc.contributor.authorBurge, Christopher B.
dc.date2022-08-11T08:08:23.000
dc.date.accessioned2022-08-23T15:53:08Z
dc.date.available2022-08-23T15:53:08Z
dc.date.issued2018-03-27
dc.date.submitted2018-06-07
dc.identifier.citation<p>bioRxiv 290007; doi: https://doi.org/10.1101/290007. <a href="https://doi.org/10.1101/290007" target="_blank">Link to preprint on bioRxiv service. </a></p>
dc.identifier.doi10.1101/290007
dc.identifier.urihttp://hdl.handle.net/20.500.14038/29290
dc.description.abstractRecursive splicing, a process by which a single intron is removed from pre-mRNA transcripts in multiple distinct segments, has been observed in a small subset of Drosophila melanogaster introns. However, detection of recursive splicing requires observation of splicing intermediates which are inherently unstable, making it difficult to study. Here we developed new computational approaches to identify recursively spliced introns and applied them, in combination with existing methods, to nascent RNA sequencing data from Drosophila S2 cells. These approaches identified hundreds of novel sites of recursive splicing, expanding the catalog of recursively spliced fly introns by 4-fold. Recursive sites occur in most very long (> 40 kb) fly introns, including many genes involved in morphogenesis and development, and tend to occur near the midpoints of introns. Suggesting a possible function for recursive splicing, we observe that fly introns with recursive sites are spliced more accurately than comparably sized non-recursive introns.
dc.language.isoen_US
dc.relationNow published in PLOS Genetics doi: 10.1371/journal.pgen.1007588
dc.rightsThe copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC 4.0 International license.
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectintrons
dc.subjectrecursive splicing
dc.subjectDrosophila melanogaster
dc.subjectmRNA
dc.subjectgenomics
dc.subjectComputational Biology
dc.subjectGenetic Phenomena
dc.subjectGenomics
dc.subjectNucleic Acids, Nucleotides, and Nucleosides
dc.titleNumerous recursive sites contribute to accuracy of splicing of long introns in flies [preprint]
dc.typePreprint
dc.source.journaltitlebioRxiv
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2524&amp;context=faculty_pubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/1518
dc.identifier.contextkey12274115
refterms.dateFOA2022-08-23T15:53:08Z
html.description.abstract<p>Recursive splicing, a process by which a single intron is removed from pre-mRNA transcripts in multiple distinct segments, has been observed in a small subset of Drosophila melanogaster introns. However, detection of recursive splicing requires observation of splicing intermediates which are inherently unstable, making it difficult to study. Here we developed new computational approaches to identify recursively spliced introns and applied them, in combination with existing methods, to nascent RNA sequencing data from Drosophila S2 cells. These approaches identified hundreds of novel sites of recursive splicing, expanding the catalog of recursively spliced fly introns by 4-fold. Recursive sites occur in most very long (> 40 kb) fly introns, including many genes involved in morphogenesis and development, and tend to occur near the midpoints of introns. Suggesting a possible function for recursive splicing, we observe that fly introns with recursive sites are spliced more accurately than comparably sized non-recursive introns.</p>
dc.identifier.submissionpathfaculty_pubs/1518
dc.contributor.departmentRNA Therapeutics Institute


Files in this item

Thumbnail
Name:
290007.full.pdf
Size:
3.940Mb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record

The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC 4.0 International license.
Except where otherwise noted, this item's license is described as The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC 4.0 International license.