4.5 Article

Nuclear-localized tiny RNAs are associated with transcription initiation and splice sites in metazoans

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NATURE STRUCTURAL & MOLECULAR BIOLOGY
卷 17, 期 8, 页码 1030-U146

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NATURE PUBLISHING GROUP
DOI: 10.1038/nsmb.1841

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资金

  1. Australian Research Council [FF0561986, DP0988851]
  2. Australian National Health and Medical Research Council [358300]
  3. Sydney Cancer Centre Foundation
  4. Cancer Institute NSW
  5. NSW Cancer Council
  6. Cure The Future Foundation
  7. Australian National Health and Medical Research Council
  8. Australian Research Council [DP0988851, FF0561986] Funding Source: Australian Research Council

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We have recently shown that transcription initiation RNAs (tiRNAs) are derived from sequences immediately downstream of transcription start sites. Here, using cytoplasmic and nuclear small RNA high-throughput sequencing datasets, we report the identification of a second class of nuclear-specific similar to 17- to 18-nucleotide small RNAs whose 3' ends map precisely to the splice donor site of internal exons in animals. These splice-site RNAs (spliRNAs) are associated with highly expressed genes and show evidence of developmental stage-and region-specific expression. We also show that tiRNAs are localized to the nucleus, are enriched at chromatin marks associated with transcription initiation and possess a 3'-nucleotide bias. Additionally, we find that microRNA-offset RNAs (moRNAs), the miR-15/16 cluster previously linked to oncosuppression and most small nucleolar RNA (snoRNA)-derived small RNAs (sdRNAs) are enriched in the nucleus, whereas most miRNAs and two H/ACA sdRNAs are cytoplasmically enriched. We propose that nuclear-localized tiny RNAs are involved in the epigenetic regulation of gene expression.

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