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Related Concept Videos

lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

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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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Types of RNA01:20

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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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Types of RNA01:23

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Overview
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 the regulation of 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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Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
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An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
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RNA Pull-down Procedure to Identify RNA Targets of a Long Non-coding RNA
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Computational methods to predict long noncoding RNA functions based on co-expression network.

Yi Zhao1, Haitao Luo, Xiaowei Chen

  • 1Key Laboratory of Intelligent Information Processing, Institute of Computing Technology, Chinese Academy of Sciences, No. 6 Kexueyuan South Road, Haidian District, Beijing, 100190, People's Republic of China.

Methods in Molecular Biology (Clifton, N.J.)
|July 25, 2014
PubMed
Summary
This summary is machine-generated.

This study introduces a computational pipeline for large-scale functional annotation of long noncoding RNAs (lncRNAs). It leverages coding-noncoding gene co-expression networks to predict lncRNA functions, addressing a gap in current research.

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Area of Science:

  • Genomics
  • Bioinformatics

Background:

  • Long noncoding RNAs (lncRNAs) are abundant in the mammalian transcriptome, but their functions are challenging to determine at scale.
  • Current methods for lncRNA functional characterization through lab experiments or structure prediction are limited.

Purpose of the Study:

  • To develop and present a computational pipeline for the large-scale functional annotation of lncRNAs.
  • To address the deficit in understanding lncRNA functions by utilizing gene co-expression networks.

Main Methods:

  • Constructed a coding-noncoding gene co-expression network using gene expression profiles, specifically in prostate cancer.
  • Nodes represent protein-coding genes or lncRNAs; edges signify co-expression based on correlation coefficients.
  • Employed model-based and hub-based sub-networks for predicting lncRNA functions.

Main Results:

  • Successfully developed a computational pipeline for lncRNA functional annotation.
  • Demonstrated the pipeline's application in constructing a co-expression network for prostate cancer data.
  • Showcased the prediction of lncRNA functions through network analysis.

Conclusions:

  • The developed computational pipeline enables large-scale functional annotation of lncRNAs.
  • Co-expression network analysis provides a viable approach for predicting lncRNA functions, particularly in disease contexts like prostate cancer.