Cellular and viral determinants of retroviral nuclear entry
Open accessAbstract
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.
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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]
Cites
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Capsid Is a Dominant Determinant of Retrovirus Infectivity in Nondividing Cells
Yamashita, M., & Emerman, M. (2004) · Journal of Virology · doi:10.1128/jvi.78.11.5670-5678.2004 · Cited by 325 · see citing works
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Clinical use of lentiviral vectors
Milone, M. C., & O’Doherty, U. (2018) · Leukemia · doi:10.1038/s41375-018-0106-0 · Cited by 930 · see citing works
“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; however, recent studies of the integration process have”
BackgroundBejarano, D. A., Peng, K., Laketa, V., Börner, K., Jost, K. L., Lucic, B., Glass, B., Lusic, M., Müller, B., & Kräusslich, H.-G. (2019) · eLife · doi:10.7554/elife.41800 · Cited by 197 · see citing works
- Authors
- Hamid, F. B., Kim, J., & Shin, C.-G.
- Affiliations
- Chung-Ang University (KR)
- Venue
- Canadian Journal of Microbiology
- Publisher
- Canadian Science Publishing
- 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
- bronze
- doi.org
- 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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