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Published on: June 30, 2013
Growth properties of HSIVnef: HIV-1 containing the nef gene from pathogenic molecular clone SIVmac239
1Institute for Molecular Biology and Genetics, Seoul National University, South Korea.
Abstract:
To elucidate the function of nef, we constructed infectious chimeric clones between human immunodeficiency virus type 1 (HIV-1) and simian immunodeficiency virus (SIV) of macaques, by deleting a part of the nef sequence from the HIV-1 genome and inserting the entire nef gene from the pathogenic molecular clone, SIVmac239. We have named this construct HSIVnef. While there was no difference in the replication kinetics of HSIVnef+ and HSIVnef- in transformed cell lines, there was a profound difference in the replication of these virus in primary cells. These data indicated that the SIV nef gene could complement the functions of the HIV-1 nef gene in the context of the HIV-1 genome, providing further evidence that results observed in the macaque model are relevant to HIV infections in man. HSIVnef is a useful model for the study of the nef gene.
Insights
The simian immunodeficiency virus (SIV) nef gene complements human immunodeficiency virus type 1 (HIV-1) nef function. This chimeric virus model, HSIVnef, aids in understanding HIV-1 nef gene roles in primary cells.
Area of Science:
- Virology
- Molecular Biology
- Immunology
Background:
- The nef gene is crucial for human immunodeficiency virus type 1 (HIV-1) replication and pathogenesis.
- Understanding the function of nef is essential for developing effective HIV-1 therapies.
- Simian immunodeficiency virus (SIV) provides a relevant model for studying HIV-1, as macaques infected with SIV exhibit AIDS-like disease.
Purpose of the Study:
- To elucidate the function of the nef gene by creating a chimeric virus between HIV-1 and SIV.
- To investigate whether the SIV nef gene can complement the function of the HIV-1 nef gene.
- To establish a useful model for studying the nef gene in the context of HIV-1 infection.
Main Methods:
- Construction of infectious chimeric clones between HIV-1 and SIVmac239, named HSIVnef.
- Deletion of a portion of the HIV-1 nef sequence and insertion of the entire SIVmac239 nef gene.
- Comparative analysis of virus replication kinetics in transformed cell lines and primary cells.
Main Results:
- No significant difference in replication kinetics was observed between HSIVnef+ and HSIVnef- in transformed cell lines.
- A profound difference in replication kinetics was observed in primary cells, indicating functional complementation by the SIV nef gene.
- The SIV nef gene demonstrated the ability to complement HIV-1 nef functions within the HIV-1 genome.
Conclusions:
- The SIV nef gene can functionally replace or complement the HIV-1 nef gene.
- Results from the macaque model using HSIVnef are relevant to human HIV-1 infections.
- The HSIVnef chimeric virus serves as a valuable model for in-depth study of nef gene function.
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