Searching journal content for articles similar to Li et al. 23 (10): 1730.

Displaying results 1-10 of 98
For checked items
  1. ...). Reads mapped to the sense strand were highly enriched on the gene transcription side, and reads mapped to the antisense strand were enriched on the opposite side, indicating that the sequencing results were highly strand specific. The read profile of unfragmented RNA showed a preference for distal sites...
  2. ...III transcripts are not polyadenylated (Sisodia et al. 1987) and thereby were depleted in our sequenced data owing to poly(A) RNA pulldown step (Supplemental Fig. S1A). Also, antisense promoters in Alu elements have been reported to produce poly(A) RNAs (Jang et al. 2019; Shah et al. 2023). We suspect...
  3. ...of the transcript, which is essential to be able to detect new antisense transcripts. As we have recently shown in S. cerevisiae, antisense transcripts can originate rapidly during evolution, providing new functionalities (Blevins et al. 2021). No dRNA-seq of S. pombe has yet been produced, limiting our knowledge...
  4. ...used to identify antisense transcripts. However, because of the overall weak expression of antisense transcripts (Pelechano and Steinmetz 2013), stranded RNA-seq has limited power to fully characterize the landscape of antisense transcription. Moreover, the strand specificity varies depending...
  5. ...Several studies support that antisense-mediated regulation may affect a large proportion of genes. Using the Illumina next-generation sequencing platform, we developed DSSS ( d irect s trand s pecific s equencing), a strand-specific protocol for transcriptome sequencing. We tested DSSS with RNA from...
  6. ...on their expression pattern, cytosolic nature, and their higher complementarity to the overlapping developmental mRNAs, we speculate that Group 1 NATs function post-transcriptionally to silence spurious expression of developmental genes.Natural antisense transcripts (NATs) are noncoding RNAs that are transcribed...
  7. ...contributors to phenotypic diversity across eukaryotes. Although short-read RNA-sequencing has increased our understanding of isoform diversity, it is challenging to accurately detect full-length transcripts, preventing the identification of many alternate isoforms. Long-read sequencing technologies have made...
  8. ...transcripts in Arabidopsis. These lncNATs could be reproducibly detected by different technical platforms, including strand-specific tiling arrays, Agilent custom expression arrays, strand-specific RNA-seq, and qRT-PCR experiments. Moreover, we investigated the expression profiles of sense–antisense pairs...
  9. ...A,B). Furthermore, 60.4% of up-regulated Y1P lncRNAs are natural antisense transcripts that could trigger transcriptional interference of sense genes (Supplemental Fig. S3C; Modarresi et al. 2012). Nascent lncRNA transcripts associated with S2P RNA Pol II were mostly down-regulated (Supplemental Fig...
  10. ...-cycle regulators INK4A, ARF, and INK4B, respectively. Next, we asked if boundary RNAs play a direct role in transcriptional activity of genes within this TAD. Using shRNAs to sense and antisense B1 and B2 CTCF sites, we observed down-regulation of INK4, ARF, INK4b, and MTAP, whereas the transcription of DDX5...
For checked items

Preprint Server