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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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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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RNA-seq03:21

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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
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The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
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Updated: Dec 13, 2025

RNA Pull-down Procedure to Identify RNA Targets of a Long Non-coding RNA
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A Heterogeneous Information Network Model for Long Non-Coding RNA Function Prediction.

Sunil Kumar P V, Adheeba Thahsin, Manju M

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    This study introduces a computational method to predict long non-coding RNA (lncRNA) functions, overcoming challenges of experimental characterization. The novel approach accurately identifies functions for thousands of lncRNAs, aiding biological research.

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    Area of Science:

    • Genomics
    • Computational Biology
    • Molecular Biology

    Background:

    • Long non-coding RNAs (lncRNAs) are increasingly identified but poorly functionally annotated.
    • Experimental methods for lncRNA functional characterization are time-consuming and costly.
    • Predicting lncRNA functions computationally is crucial for advancing research.

    Purpose of the Study:

    • To develop an accurate computational method for predicting lncRNA functions.
    • To address the challenge of low functional annotation rates in lncRNAs.
    • To provide a valuable tool for researchers investigating lncRNA roles.

    Main Methods:

    • Constructed a Heterogeneous Information Network (HIN) integrating lncRNA-protein, lncRNA co-expression, and protein-protein interaction data.
    • Employed a meta-path based measure, AvgSim, within the HIN to predict lncRNA functions.
    • Evaluated the model's performance on a large set of lncRNAs.

    Main Results:

    • Successfully predicted functions for 2,695 out of 2,758 lncRNAs with 73.68% accuracy.
    • The proposed method outperformed existing state-of-the-art approaches on an independent test set.
    • Case studies on HOTAIR and H19 validated predicted functions against existing literature.

    Conclusions:

    • The developed computational method offers an efficient and accurate approach for lncRNA function prediction.
    • This tool can significantly accelerate the functional characterization of newly identified lncRNAs.
    • The freely available script and data facilitate broader adoption and further research.