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Related Concept Videos

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Regulated mRNA Transport

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In eukaryotes, transcription and translation are compartmentalized; an mRNA is first synthesized in the nucleus and then selectively transported to the cytoplasm for protein synthesis. Before transport, a pre-mRNA undergoes several steps of post-transcriptional modifications including splicing, 5' capping, and the addition of a poly-adenine tail. Various proteins bind to the pre-mRNA during these modifications. The mRNA transport takes place with the help of multiple proteins playing...
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Nuclear protein sorting is the selective trafficking of histones, polymerases, gene regulatory proteins into the nucleus and exporting RNAs and ribosomes to the cytosol. It is a tightly controlled process that regulates gene expression within a cell.
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The organelle-specific signaling sequences direct proteins synthesized in the cytosol to their final destination like ER, mitochondria, peroxisomes, etc. Some of the proteins directed to ER are then trafficked via vesicles to other organelles within the cell or the extracellular environment through the Golgi complex. For example, the rough ER synthesizes soluble proteins for transportation to the lysosomes or secretion out of the cell. It can also synthesize transmembrane proteins that can...
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During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
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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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Proteins targeted to the nucleus carry short stretches of amino acid sequences called the nuclear localization signal or NLS. Classical nuclear localization signals are of two types: monopartite and bipartite NLS. Monopartite classical NLS (cNLS) consists of a single cluster of 4-8 amino acids. Bipartite cNLS consists of two clusters of  2-3 amino acids and a 9-12 residue long proline-rich linker bridging the two clusters. Signal clusters are rich in positively charged amino acids such as...
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Updated: Sep 3, 2025

Identification of Circular RNAs using RNA Sequencing
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Circ-LocNet: A Computational Framework for Circular RNA Sub-Cellular Localization Prediction.

Muhammad Nabeel Asim1,2, Muhammad Ali Ibrahim1,2, Muhammad Imran Malik3

  • 1German Research Center for Artificial Intelligence (DFKI), 67663 Kaiserslautern, Germany.

International Journal of Molecular Sciences
|July 28, 2022
PubMed
Summary
This summary is machine-generated.

This study introduces Circ-LocNet, a computational tool to predict circular RNA (circRNA) sub-cellular localization. Machine learning, particularly tree-based classifiers with sequence descriptors, accurately determines circRNA location, aiding disease and drug development research.

Keywords:
circular RNAclassificationmachine learningnon-coding RNAnucleotide frequencynucleotide physico-chemical propertiessub-cellular localization datasetsubcellular localizationweb server

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Area of Science:

  • Molecular Biology
  • Bioinformatics
  • Genomics

Background:

  • Circular RNAs (circRNAs) are novel non-coding RNAs with largely unknown functions.
  • Understanding circRNA sub-cellular localization is crucial for elucidating their roles in physiological processes, disease, and drug development.
  • Current methods for detecting circRNA location rely on time-consuming wet experimental approaches.

Purpose of the Study:

  • To develop a computational framework, Circ-LocNet, for precise prediction of circRNA sub-cellular localization.
  • To evaluate the effectiveness of various sequence descriptors and machine learning classifiers for circRNA localization prediction.
  • To explore the impact of sequence descriptor fusion on prediction accuracy.

Main Methods:

  • Development of Circ-LocNet, a machine learning framework for circRNA sub-cellular localization.
  • Extrinsic evaluation of 7 residue frequency-based, residue order and frequency-based, and physio-chemical property-based sequence descriptors.
  • Utilized five widely used machine learning classifiers and assessed K-order sequence descriptor fusion (2nd to 7th order).

Main Results:

  • Standalone residue frequency-based sequence descriptors with tree-based classifiers showed suitability for predicting circRNA sub-cellular localization.
  • K-order heterogeneous sequence descriptors fusion combined with tree-based classifiers achieved the most accurate predictions.
  • Circ-LocNet provides a robust computational baseline for novel circRNA localization determination.

Conclusions:

  • Computational prediction of circRNA sub-cellular localization is feasible and accurate using machine learning.
  • Tree-based classifiers and sequence descriptor fusion are key to enhancing prediction accuracy.
  • Circ-LocNet facilitates future research into circRNA functions, disease associations, and therapeutic strategies.