A massively parallel 3′ UTR reporter assay reveals relationships between nucleotide content, sequence conservation, and mRNA destabilization

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Figure 2.
Figure 2.

Inverse relationship of 3′ UTR GC content and gene expression is reproducible across several experimental modalities and cell types. (A) GC content of 3′ UTR inserts of fast-UTR library transduced BEAS-2B cells FACS-sorted for high or low GFP fluorescence. (B) mRNA half-life of inserts of high or low protein expressing 3′ UTR inserts from A in BEAS-2B cells. (C) Steady-state mRNA abundance of inserts of high or low protein expressing 3′ UTR inserts from A in three human cell lines. For AC, P-values represent Welch's unequal variance t-test between high and low protein expressing inserts. (DG) Correlation between 3′ UTR insert GC content and steady-state mRNA abundance (D–F) or mRNA half-life (G) for fast-UTR assays in indicated cell lines. (r) Pearson correlation coefficient, P-value tests null hypothesis that correlation is equal to 0.

This Article

  1. Genome Res. 29: 896-906

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