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  1. ...alternative TISs are shared across species and also support the findings of previous studies that uORFs are conserved across plants species and are predicted to be initiated from both AUG and non-AUG codons (Hayden and Jorgensen 2007; Jorgensen and Dorantes-Acosta 2012; Takahashi et al. 2012; Vaughn et al...
  2. ...of relying on sequence conservation and 3-nt periodicity in revealing protein-coding regions for ORF annotation. Thus, complementary to comparative-genomic approaches and the CHX-based ribosome profiling analyses that have successfully characterized some alternative AUG and nonAUG TIS-initiated ORFs...
  3. ...-seq reads fell into annotated 5′ UTRs (Fig. 1C), albeit with pronounced transcript-specific variability (Supplemental Fig. S3A), suggestive of abundant uORF usage in the liver. uORFs are short and often poorly conserved (Churbanov et al. 2005) and frequently initiate at near-cognate (non-AUG) start codons...
  4. ...to uORFs affected ribosome occupancy of the main coding region using a linear regression framework. The absolute value of the effect size from the regression was plotted against the P-value of association. For 17 uORF changes shown with red circles, the association was solely with ribosome occupancy...
  5. .... 2016; Pueyo et al. 2016a; Delcourt et al. 2017; Hsu and Benfey 2017; Willems et al. 2017). Three detection methods—ribosome profiling, proteogenomics, and conservation signatures—have been used to identify likely translated and functional alternative ORFs, as further discussed later in this review...
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  6. ...function pathways, such as ribosome and RNA transport (median 5′-UTR lengths ranging from 37–63 bp) (Supplemental Fig. S2C). These results support the hypothesis that 5′-UTR length, which is primarily determined by the location of TSSs, relates to gene functions and their expression profiles (Lin and Li...
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