Study / S2NV89LAP2017-11-02
Deep learning of the regulatory grammar of yeast 5′ untranslated regions from 500,000 random sequences
Josh T. Cuperus, Benjamin Groves, Anna Kuchina, Alexander B. Rosenberg, Nebojsa Jojic et al.
About this study
Our ability to predict protein expression from DNA sequence alone remains poor, reflecting our limited understanding of cis-regulatory grammar and hampering the design of engineered genes for synthetic biology applications. Here, we generate a model that predicts the protein expression of the 5′ untranslated region (UTR) of mRNAs in the yeast Saccharomyces cerevisiae. We constructed a library of half a million 50-nucleotide-long random 5′ UTRs and assayed their activity in a massively parallel growth selection experiment. The resulting data allow us to quantify the impact on protein expression of Kozak sequence composition, upstream open reading frames (uORFs), and secondary structure. We trained a convolutional neural network (CNN) on the random library and showed that it performs well at predicting the protein expression of both a held-out set of the random 5′ UTRs as well as native S. cerevisiae 5′ UTRs. The model additionally was used to computationally evolve highly active 5′ UTRs. We confirmed experimentally that the great majority of the evolved sequences led to higher protein expression rates than the starting sequences, demonstrating the predictive power of this model.
Full author list & citation
Josh T. Cuperus, Benjamin Groves, Anna Kuchina, Alexander B. Rosenberg, Nebojsa Jojic, Stanley Fields, Georg Seelig. Deep learning of the regulatory grammar of yeast 5′ untranslated regions from 500,000 random sequences. 2017-11-02. https://doi.org/10.1101/gr.224964.117
Experiments 3
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Start, midpoint, and endpoint sequences selected by the CNN from random and native 5′ UTRs were synthesized in the same HIS3 reporter system and tested under three 3-AT selection strengths. The processed table contains the complete-value rows from the supplemental forward-engineering growth table and derives within-parent changes from the starting sequence.
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A pooled low-copy p415-CYC1-HIS3 plasmid library containing 50-nt random 5′ UTR inserts was transformed into BY4741 yeast lacking a native HIS3 copy. The abundance of 489,348 detected variants was measured before and after competitive histidine selection, providing a sequence-linked protein-expression proxy.
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A pooled low-copy p415-CYC1-HIS3 plasmid library containing up to 50-nt fragments from known Saccharomyces cerevisiae native 5′ UTRs was transformed into BY4741 yeast lacking a native HIS3 copy. The abundance of 11,856 detected native fragments was measured before and after competitive histidine selection to estimate sequence-dependent protein expression.