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  1. ...editing site A become paired after editing, whereas only 4% of the paired A become unpaired after editing (Fig. 4C). To examine the impact of the editing on modulating sense miRNA targeting, we experimentally tested six miRNA-ATs in which the editing events altered predicted secondary structures and did...
  2. ...-type miR-200b expression. We further experimentally showed that, in contrast to wild-type miRNA, the edited miR-200b can promote cell invasion andmigration through its impaired ability to inhibit ZEB1/ZEB2 and acquired concomitant ability to repress new targets, including LIFR, a well...
  3. ...as regulators by altering the number of RBP and miRNA binding sites. Furthermore, we identified potential sQTLs affecting the 3′ UTR length of the CD47 gene in sperm cells, which have a significant impact on reproductive traits. Cross-species analysis indicated that APA lengths are generally longer in brain...
  4. ...a similarly modest reduction in miRNA levels in these libraries (Supplemental Fig. S2E; Supplemental Table S4). The comparable effect of dcr-1 RNAi on miRNAs, which are known Dicer substrates, and 23H-RNAs further supports a role for Dicer in 23H-RNA biogenesis (Grishok et al. 2001; Hutvágner et al. 2001...
  5. ...-interacting RNAs (piRNAs), which are complementary to or derived from TEs. piRNAs are expressed primarily in the gonad and are larger than miRNAs (Mani and Juliano 2013; Czech and Hannon 2016). Once bound to an RNA target, PIWI proteins cleave their target precisely 10 nt from the 5′ end of the complementary pi...
  6. ...and suggests a diverse impact of human genetic variation on miRNA biogenesis.Mature miRNAs are derived from hairpin-containing primary transcripts (pri-miRNAs). For the vast majority of miRNAs, pri-miRNAs are processed in the nucleus by the Microprocessor complex, containing DROSHA, DGCR8, and other proteins...
  7. ...transcriptase, and (RH) RNase H. Blue and red lines indicate primer binding sites (PBSs) and polypurine tracts (PPTs). The 21- to 22-nt small RNA (sRNA) data were obtained from a previous study (Creasey et al. 2014). Target positions of miRNAs are indicated as arrows (for details, see Supplemental Table S4...
  8. ...were coupled with other features, including genomic organization, transcription rates, structural heterogeneity (isomiRs), and target abundance, measured through quantitative experimental approaches. This comprehensive analysis highlighted functional mechanisms that mediate miRNA degradation, as well...
  9. ...). Then, we asked whether the deaminases that target tRNA also affect mRNA. Unlike in tRNA, there was no difference in the mRNA editing patterns between mutants and wild-type strains. Other types of RDDs were also unchanged in the deaminase mutants. The relative abundance of all 12 types is highly similar...
  10. ...of target mRNAs. For example, in mature B lymphocytes, a 3′ fragment derived from tRNAGlyGCC (referred to as 3′-tsRNAGlyGCC) has activities characteristic of a miRNA, including the capacity of binding to all four human AGOs and gene silencing via target sites in 3′ UTRs (Maute et al. 2013). In addition, ts...
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