scholarly journals COSSMO: Predicting Competitive Alternative Splice Site Selection using Deep Learning

2018 ◽  
Author(s):  
Hannes Bretschneider ◽  
Shreshth Gandhi ◽  
Amit G Deshwar ◽  
Khalid Zuberi ◽  
Brendan J Frey

AbstractMotivationAlternative splice site selection is inherently competitive and the probability of a given splice site to be used also depends strongly on the strength of neighboring sites. Here we present a new model named Competitive Splice Site Model (COSSMO), which explicitly models these competitive effects and predict the PSI distribution over any number of putative splice sites. We model an alternative splicing event as the choice of a 3’ acceptor site conditional on a fixed upstream 5’ donor site, or the choice of a 5’ donor site conditional on a fixed 3’ acceptor site. We build four different architectures that use convolutional layers, communication layers, LSTMS, and residual networks, respectively, to learn relevant motifs from sequence alone. We also construct a new dataset from genome annotations and RNA-Seq read data that we use to train our model.ResultsCOSSMO is able to predict the most frequently used splice site with an accuracy of 70% on unseen test data, and achieve an R2 of 60% in modeling the PSI distribution. We visualize the motifs that COSSMO learns from sequence and show that COSSMO recognizes the consensus splice site sequences as well as many known splicing factors with high specificity.AvailabilityOur dataset is available from http://cossmo.deepgenomics.com.Contactfrey@deepgenomics.comSupplementary informationSupplementary data are available at Bioinformatics online.

1987 ◽  
pp. 97-112 ◽  
Author(s):  
JAMES L. MANLEY ◽  
JONATHAN C.S. NOBLE ◽  
XIN-YUAN FU ◽  
HUI GE

2003 ◽  
Vol 278 (20) ◽  
pp. 18241-18248 ◽  
Author(s):  
Ute Raffetseder ◽  
Björn Frye ◽  
Thomas Rauen ◽  
Karsten Jürchott ◽  
Hans-Dieter Royer ◽  
...  

2018 ◽  
Vol 34 (13) ◽  
pp. i429-i437 ◽  
Author(s):  
Hannes Bretschneider ◽  
Shreshth Gandhi ◽  
Amit G Deshwar ◽  
Khalid Zuberi ◽  
Brendan J Frey

1988 ◽  
Vol 8 (6) ◽  
pp. 2610-2619 ◽  
Author(s):  
D E Lowery ◽  
B G Van Ness

The processing of a number of kappa-immunoglobulin primary mRNA (pre-mRNA) constructs has been examined both in vitro and in vivo. When a kappa-immunoglobulin pre-mRNA containing multiple J segment splice sites is processed in vitro, the splice sites are used with equal frequency. The presence of signal exon, S-V intron, or variable (V) region has no effect on splice site selection in vitro. Nuclear extracts prepared from a lymphoid cell line do not restore correct splice site selection. Splice site selection in vitro can be altered by changing the position or sequence of J splice donor sites. These results differ from the processing of similar pre-mRNAs expressed in vivo by transient transfection. The 5'-most J splice donor site was exclusively selected in vivo, even in nonlymphoid cells, and even in transcripts where in vitro splicing favored a 3' J splice site. The in vitro results are consistent with a model proposing that splice site selection is influenced by splice site strength and proximity; however, our in vivo results demonstrate a number of discrepancies with such a model and suggest that splice site selection may be coupled to transcription or a higher-order nuclear structure.


1988 ◽  
Vol 8 (6) ◽  
pp. 2610-2619
Author(s):  
D E Lowery ◽  
B G Van Ness

The processing of a number of kappa-immunoglobulin primary mRNA (pre-mRNA) constructs has been examined both in vitro and in vivo. When a kappa-immunoglobulin pre-mRNA containing multiple J segment splice sites is processed in vitro, the splice sites are used with equal frequency. The presence of signal exon, S-V intron, or variable (V) region has no effect on splice site selection in vitro. Nuclear extracts prepared from a lymphoid cell line do not restore correct splice site selection. Splice site selection in vitro can be altered by changing the position or sequence of J splice donor sites. These results differ from the processing of similar pre-mRNAs expressed in vivo by transient transfection. The 5'-most J splice donor site was exclusively selected in vivo, even in nonlymphoid cells, and even in transcripts where in vitro splicing favored a 3' J splice site. The in vitro results are consistent with a model proposing that splice site selection is influenced by splice site strength and proximity; however, our in vivo results demonstrate a number of discrepancies with such a model and suggest that splice site selection may be coupled to transcription or a higher-order nuclear structure.


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