Analysis of coordinated skipped exon pairs using single molecule sequencing technology

Alternative splicing of mRNA transcripts is a significant step in the production of functioning protein. This process is a major source of molecular diversity, as numerous mRNA and protein products can arise from a single gene locus, and incorrect regulation has been implicated in numerous diseases. While many robust methods exist to study genome-wide single exon splicing patterns, no methodology has been established to accurately examine multiple events over a single isoform. Read sequencing technology has been the limiting factor; however, the recent development of real time, single molecule read sequencing provides an opportunity to characterize alternative splicing on the whole transcript level. We propose a computational approach to detect the splicing patterns of pairs of alternative exons in the same gene. Using a sequenced full-length cDNA library of human MCF-7 transcripts, we are able to evaluate 761 genes and identify three with evidence of non-random splicing of distinct nonadjacent alternative exons, all of which are frame-preserving and biased toward mutual inclusion. Characterizing their protein products reveals that the domain, secondary, and tertiary structures of the isoforms are not significantly affected. Low read coverage proves to be the greatest hindrance to a larger result set, but overall we provide a computational proof of concept for studying coordinated alternative splicing events on a transcriptomic scale.

Department dc:contributor.department

Massachusetts Institute of Technology. Computational and Systems Biology Program.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2014

Author dc:creator

• Adadey, Asa (Asa Owuraku)

Advisor dc:contributor.advisor

• Christopher Burge.

• Computational and Systems Biology Program.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/93043

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/93043