Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Nuclear Localization Signals and Import01:46

Nuclear Localization Signals and Import

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...
Nuclear Protein Sorting01:34

Nuclear Protein Sorting

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.
Proteins targeted to the nucleus carry nuclear localization signals or NLS recognized by import receptors in the cytosol. Similarly, proteins with nuclear export signals are recognized by export receptors. Import and export receptors are...
Leaky Scanning02:28

Leaky Scanning

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 stands for...
Regulation of Nuclear Protein Sorting01:45

Regulation of Nuclear Protein Sorting

Nuclear protein sorting regulates nucleus composition and gene expression, crucial for determining the fate of a eukaryotic cell. Hence, the entry and exit of molecules across the nuclear envelope is a tightly controlled process. Nuclear protein sorting can be inhibited by one of the following ways: 1) masking cargo signal sequences, 2) modifying the nuclear receptor's affinity for cargo, 3) controlling the nuclear pore size, 4) retaining the cargo during its transit to the cytosol or the...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Mitochondrial activity promotes neutrophil degranulation and endothelial dysfunction in systemic infections.

EMBO molecular medicine·2026
Same author

Visualization of Bluetongue Virus RNA Segment Networks in Infected Cells: Multipartite Genomic RNA Assortment Is Independent of Viral Proteins NS2 and VP6.

Viruses·2026
Same author

Antibody-drug-conjugates prepared with Peptide Asparaginyl Ligases achieve strong in vitro and in vivo anti-tumor activity.

Molecular cancer therapeutics·2026
Same author

In Silico-Enabled Discovery and Development of Potent and Selective CDK11 Inhibitors.

ChemMedChem·2026
Same author

Evaluation of metformin's effect on 5-fluorouracil-induced cardiotoxicity through cellular protection.

Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences·2026
Same author

Correction to "Discovery of an Orally Bioavailable Reversible Covalent SARS-CoV-2 M<sup>pro</sup> Inhibitor with Pan-Coronavirus Activity".

Journal of medicinal chemistry·2025

Related Experiment Video

Updated: May 10, 2026

Portable Paper-Based Immunoassay Combined with Smartphone Application for Colorimetric and Quantitative Detection of Dengue NS1 Antigen
06:00

Portable Paper-Based Immunoassay Combined with Smartphone Application for Colorimetric and Quantitative Detection of Dengue NS1 Antigen

Published on: January 26, 2024

Serotype-specific differences in dengue virus non-structural protein 5 nuclear localization.

Holger Hannemann1, Po-Yu Sung, Han-Chen Chiu

  • 1School of Cellular and Molecular Medicine, Faculty of Medical and Veterinary Sciences, University of Bristol, University Walk, Bristol BS8 1TD, United Kingdom.

The Journal of Biological Chemistry
|June 18, 2013
PubMed
Summary
This summary is machine-generated.

Dengue virus non-structural protein 5 (NS5) shows distinct nuclear localization patterns across its four serotypes. This difference, not linked to nuclear export or IL-8 expression, suggests NS5 nuclear entry has an auxiliary role in specific dengue virus serotype lifecycles.

Keywords:
DengueFlavivirusesNuclear TransportPositive Strand RNA VirusesViral PolymeraseVirology

More Related Videos

Identification of Plasmodesmal Localization Sequences in Proteins In Planta
08:07

Identification of Plasmodesmal Localization Sequences in Proteins In Planta

Published on: August 15, 2017

Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses
12:20

Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses

Published on: December 29, 2015

Related Experiment Videos

Last Updated: May 10, 2026

Portable Paper-Based Immunoassay Combined with Smartphone Application for Colorimetric and Quantitative Detection of Dengue NS1 Antigen
06:00

Portable Paper-Based Immunoassay Combined with Smartphone Application for Colorimetric and Quantitative Detection of Dengue NS1 Antigen

Published on: January 26, 2024

Identification of Plasmodesmal Localization Sequences in Proteins In Planta
08:07

Identification of Plasmodesmal Localization Sequences in Proteins In Planta

Published on: August 15, 2017

Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses
12:20

Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses

Published on: December 29, 2015

Area of Science:

  • Virology
  • Molecular Biology
  • Immunology

Background:

  • Dengue virus (DENV) is a major arthropod-borne viral disease.
  • DENV non-structural protein 5 (NS5) has crucial enzymatic roles in viral RNA capping and replication within the host cytoplasm.
  • Previous research indicated DENV-2 NS5 accumulates in the nucleus during infection.

Purpose of the Study:

  • To investigate the nuclear localization patterns of NS5 across all four DENV serotypes.
  • To identify the mechanisms underlying differential NS5 nuclear localization.
  • To determine the functional significance of NS5 nuclear localization in the DENV lifecycle.

Main Methods:

  • Comparative analysis of NS5 localization for DENV-1, -2, -3, and -4.
  • Investigation of nuclear export mechanisms using DENV-2 and DENV-4 NS5.
  • Identification of nuclear localization sequences (NLS) and interactions with importin-α isoforms.
  • siRNA-mediated knockdown of importin-α and importin-β.
  • Assessment of IL-8 gene expression levels.

Main Results:

  • Significant serotypic differences in NS5 nuclear localization were observed: DENV-2 and -3 NS5 accumulated in the nucleus, while DENV-1 and -4 NS5 were primarily cytoplasmic.
  • The cytoplasmic localization of DENV-4 NS5 was attributed to the absence of a functional NLS, not rapid nuclear export.
  • Importin-β, but not importin-α isoforms, played a role in DENV-2 NS5 nuclear import.
  • Serotypic differences in NS5 nuclear localization did not correlate with altered IL-8 gene expression.

Conclusions:

  • NS5 nuclear localization exhibits serotype-specific variations in dengue virus.
  • The absence of a functional NLS explains the cytoplasmic retention of DENV-4 NS5.
  • Nuclear localization of NS5 is not essential for viral replication but likely serves an auxiliary function in specific DENV serotypes.