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lncRNA - Long Non-coding RNAs02:39

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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
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As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
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Three main types of RNA are involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). These RNAs perform diverse functions and can be broadly classified as protein-coding or non-coding RNA. Non-coding RNAs play important roles in regulating gene expression in response to developmental and environmental changes. Non-coding RNAs in prokaryotes can be manipulated to develop more effective antibacterial drugs for human or animal use.
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Identification of long non-coding RNA in the horse transcriptome.

E Y Scott1, T Mansour2,3, R R Bellone2,4

  • 1Department of Animal Science, University of California, Davis, USA.

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|July 6, 2017
PubMed
Summary

Researchers developed the most extensive equine long non-coding RNA (lncRNA) database, identifying 20,800 candidate lncRNA transcripts. This database characterizes intergenic RNA sequences in the horse genome, providing a foundational resource for future equine research.

Keywords:
Equine transcriptomeIntergenicLong non-coding RNA

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Area of Science:

  • Genomics
  • Transcriptomics
  • Molecular Biology

Background:

  • Equine genome research has primarily focused on protein-coding RNA.
  • Intergenic regions in the horse genome, detected by RNA-seq, remain largely uncharacterized.
  • Previous equine transcriptome studies provide a basis for lncRNA discovery.

Purpose of the Study:

  • To create the deepest and most expansive equine long non-coding RNA (lncRNA) database.
  • To characterize transcribed sequences within equine intergenic regions.
  • To annotate novel lncRNA candidates using established human annotation approaches.

Main Methods:

  • RNA sequencing (RNA-seq) data from eight equine tissues were analyzed.
  • Intergenic reads and novel gene categories were utilized for lncRNA identification.
  • A filtering approach based on size, expression, protein-coding potential, and proximity to protein-coding genes was applied.

Main Results:

  • A comprehensive equine lncRNA database containing 20,800 candidate transcripts was established.
  • Identified lncRNA candidates exhibit characteristic features such as low expression, low exon diversity, and low sequence conservation.
  • This represents the most extensive catalog of equine lncRNAs to date.

Conclusions:

  • The developed equine lncRNA database serves as a foundational resource for understanding non-coding RNA in horses.
  • This study begins to characterize the vast RNA-seq reads originating from equine intergenic regions.
  • The findings pave the way for deeper investigations into the functional roles of lncRNAs in the equine genome.