Searching journal content for articles similar to Li et al. 24 (5): 775.

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  1. ...that poly(A)-selected RNA sequencing is not an accurate reflection of true mRNA levels before ZGA. (B) FZNF expression from rRNA-depleted reads, before ZGA. (C) Maternally deposited genes are significantly older, whereas early-stage FZNFs are young and generally unique to D. rerio. Ages were quantified...
  2. ...decay pathways during zebrafish MZT. By using a massively parallel reporter assay, we identified cis-regulatory sequences in the 3′ UTR, including U-rich motifs that are associated with increased mRNA stability. In contrast, miR-430 target sequences, UAUUUAUU AU-rich elements (ARE), CCUC, and CUGC...
  3. ...the localization (Bullock et al. 2010), splicing (Buratti and Baralle 2004), and translation (Ding et al. 2014) of mRNAs. As a result, secondary structure influences nearly every processing step in the life cycle of transcripts (Vandivier et al. 2016).Secondary structures can have another effect: They act...
  4. ...and protein expression levels following the dismantling of the most abundant C. elegans miRNA family, which indicate that miR-58 family members exert both translation inhibition and mRNA degradation on their targets, with eventual mRNA degradation being the dominant consequence of miRNA repression. Results...
  5. ....] Together with a protein member of the Argonaute family, microRNAs (miRNAs) constitute the RNA-induced silencing complex (RISC), which represses specific mRNA targets by translation inhibition and mRNA decay (Iwakawa and Tomari 2015). Target recognition is typically mediated by imperfect base...
  6. ...that refining our knowledge of their roles in TP53-signaling networks and their gene targets is crucial to achieving a greater understanding of tumorigenesis. Importantly, miRNAs only become active regulators of their mRNA targets once they interact with AGO1-4 proteins, the key components of the RNA...
  7. ...changes after perturbations of these small RNAs are only partially explained by predicted miRNA/siRNA targeting. Targeting may be modulated by other mRNA sequence elements such as binding sites for the hundreds of RNA binding proteins (RNA-BPs) expressed in any cell, and this aspect has not been...
  8. ...of zebrafish by DND1 protein (Kedde et al. 2007)—involve interactions of U-rich elements, and a study of mRNA decay (Yang et al. 2003) also identified a number of AU-rich elements that positively correlated with degradation rate. Consistent with the nucleotide bias, the energy required to open the secondary...
  9. ...RNAs that are experimentally detectable in frogs, mice, and humans. By combining the small RNA sequencing with mRNA profiling at the different developmental stages, we identify a new class of small noncoding RNAs that we name siteRNAs, which align in clusters to introns of protein-coding genes. We show that site...
  10. ...al. 2000; Bernstein et al. 2001; Elbashir et al. 2001; Grishok et al. 2001; Ketting et al. 2001; Knight and Bass 2001). Argonaute proteins associate with siRNA duplexes, discarding one strand and retaining the other, which then acts as a guide to direct silencing of target messenger RNAs (mRNAs...
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