Cited by 48HIV Research and TreatmentNuclear Structure and FunctionHIV/AIDS drug development and treatment

Cellular and viral determinants of retroviral nuclear entry

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Hamid, Faysal Bin, Kim, Jinsun, Shin, Cha-Gyun·2016·Canadian Journal of Microbiology

Abstract

Retroviruses must integrate their cDNA into the host genome to generate proviruses. Viral DNA–protein complexes interact with cellular proteins and produce pre-integration complexes, which carry the viral genome and cross the nuclear pore channel to enter the nucleus and integrate viral DNA into host chromosomal DNA. If the reverse transcripts fail to integrate, linear or circular DNA species such as 1- and 2-long terminal repeats are generated. Such complexes encounter numerous cellular proteins in the cytoplasm, which restrict viral infection and protect the nucleus. To overcome host cell defenses, the pathogens have evolved several evasion strategies. Viral proteins often contain nuclear localization signals, allowing entry into the nucleus. Among more than 1000 proteins identified as required for HIV infection by RNA interference screening, karyopherins, cleavage and polyadenylation specific factor 6, and nucleoporins have been predominantly studied. This review discusses current opinions about the synergistic relationship between the viral and cellular factors involved in nuclear import, with focus on the unveiled mysteries of the host–pathogen interaction, and highlights novel approaches to pinpoint therapeutic targets.

Integrity signals

Registry

Crossref · 10.1139/cjm-2015-0350

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6 of 6 references verified0 citation errors · 0 not checkable

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  • The process of transporting the reverse transcription complex from the cellular envelope to the chromatin of the cell is active, requiring energy.

    “The process of transporting the RTC from the cellular envelope to the chromatin of the cell is active, requiring energy [15], and it remains under-investigated;”

    From Clinical use of lentiviral vectors (2018) · cites this paper as [15]

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Authors
Hamid, F. B., Kim, J., & Shin, C.-G.
Affiliations
Chung-Ang University (KR)
Venue
Canadian Journal of Microbiology
Published
2016-01
Volume
62
Issue
1
Pages
1-15
ISSN
  • 0008-4166 (ISSN-L)
  • 1480-3275
OpenAlex
W2144145035
Cited by
48
References
6
Citations by year
2025: 2 · 2024: 1 · 2023: 2 · 2022: 2 · 2021: 5 · 2020: 4 · 2019: 7 · 2018: 10 · 2017: 10 · 2016: 5
FWCI
1.12
Type
journal article
Language
en
Open access
Locations
  • Canadian Journal of Microbiology (publishedVersion)
  • PubMed (publishedVersion)
  • TSpace (University of Toronto) (acceptedVersion)
Funders
  • National Research Foundation
  • National Research Foundation of Korea
Topics
  • Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
  • Health Sciences › Medicine › Infectious Diseases › HIV/AIDS drug development and treatment
Keywords
HIV, preintegration complex, nuclear import, nuclear localization signal, karyopherins, nucleoporins, CAF-1, long terminal repeat, host-pathogen interaction, host restriction factors, antiviral drug targets
MeSH terms
Animals, Cell Nucleus, Humans, Retroviridae, Transcription Factors, Viral Proteins, Gene Products, gag, Active Transport, Cell Nucleus, Nuclear Pore Complex Proteins, beta Karyopherins, mRNA Cleavage and Polyadenylation Factors, Adaptor Proteins, Signal Transducing, Virus Internalization, Host-Pathogen Interactions

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