Searching journal content for articles similar to Espinar et al. 28 (4): 509.

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  1. ....ricci@ens-lyon.org, melissa.moore@umassmed.eduAbstractmRNA translation and decay are tightly interconnected processes both in the context of mRNA quality-control pathways and for the degradation of functional mRNAs. Cotranslational mRNA degradation through codon usage, ribosome collisions, and the recruitment of specific...
  2. ...) upstream of the uORF stop codon (orange dashed line) suggests that multiple ribosomes stack in this region. Accumulation of the PARE-seq reads (highlighted by pink dashed lines) occurs at 13 nt upstream of the corresponding Ribo-seq peaks, supporting cotranslational mRNA decay in this region. The shift...
  3. ...) ribosomes. For this purpose, we set up a run-off experiment and determined the ratio between polysome-associated and monosome-associated mRNAs following harringtonine treatment. Control (shGFP) and shTRAP1 HeLa cells were treated for 2 min with harringtonine and fractionated, and the number of transcripts...
  4. ...levels: RNA transcript, open reading frames (ORFs), and finally protein sequences (Reixachs-Solé and Eyras 2022). The complex interplay between the changes occurring to AS variants and their ORF and protein products is hard to characterize and quantify. Changes in mRNA sequence may lead to nonlinear...
  5. ...data (Fig. 3A). This new normalization method allows rate estimation from labeled and total quantities alone (Methods). Our published median half-life for Sc mRNAs (Miller et al. 2011) enabled determination of the median Sp half-life relative to Sc (Supplemental Fig. S2). We measured growth curves...
  6. ...proteins). The ABC neighborhood (Fig. 4A) of the PriOmics-CIG model comprises in total 19 peptides from 12 different proteins, in which the tryptic peptide at the protein N terminus of PDLIM1 ([1Ac]-TTQQIDLQPGPWGFR) was acetylated after cotranslational cleavage of the N-terminal methionine by methionine...
  7. ...secondary structures in lncRNA.G4s form in certain guanine-rich regions through the self-assembly of guanines into planar quartets, which are stacked into a three-dimensional structure. G4 formation can alter gene expression by inhibiting initiation complex binding at mRNA transcripts, recruiting splicing...
  8. ...and, hence, to reduction of the time spent by ribosomes on each mRNA, thereby increasing the pool of free ribosomes available in the cell, which ultimately allows a higher cellular growth rate (Bulmer 1991). Second, the usage of synonymous codons decoded by the most abundant tRNAs increases...
  9. ...(Wang et al. 2008), inducing premature ribosome drop-off (e.g., Petersen et al. 2006), or co-translational or peri-translational proteolysis (Nottrott et al. 2006). Considerable evidence has also accumulated to indicate that target mRNA deadenylation and subsequent degradation can be an important...
  10. ...primarily membrane and secreted proteins Specific mRNA features might allow coregulation of functionally related proteins. To determine whether themRNAs translationally regulated by Dhh1 are functionally linked, we performed Gene Ontology (GO) analysis (Fig. 5E,F). Genes translationally activated byDhh1...
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