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Deciphering the molecular mechanisms of HIV DNA nuclear import and the impact of 3D genome organization on integration site selection

Project description

Deciphering cellular mechanisms of HIV infection

HIV is a retrovirus that induces a wide range of pathologies in different animal species. It can incorporate its DNA into that of both dividing and non-dividing host cells. The mechanisms are not fully understood, yet are critical to the development of safer and more effective targeted antiviral therapies. RetroChrom is using high-tech methods to follow the viral DNA of HIV-1, the strain responsible for AIDS worldwide, as it moves through the cell. Scientists hope to elucidate the mechanisms underlying its integration into the host DNA, as well as factors modulating those processes, filling an important knowledge gap in the aetiology of AIDS.

Objective

Chromosomes of eukaryotes adopt highly dynamic and complex hierarchical structures in the nucleus. The three-dimensional (3D) organization of chromosomes profoundly affects DNA functions, primarily transcription. During retroviral infection, histone-free viral DNA copy is synthesized from viral genomic RNA. vDNA will ultimately integrate into the host genome to ensure its maintenance and expression. Understanding retrovirus-host interactions at the genomic level, and the peculiar mechanisms by which lentiviruses, including HIV-1, and their related gene transfer vectors, are imported into the nucleus, loaded with nucleosomes, integrate in, and interact with, the human genome will provide valuable information about lentiviral replication and establish the basis for the development of safer and more efficacious lentiviral vectors for human gene therapy. Our objectives are: 1-To identify and characterize cellular proteins associated with the HIV-1 PIC, and determine their roles in nuclear import and/or integration. 2-To explore the role of the epigenome of unintegrated vDNA in HIV-1 gene expression from unintegrated and integrated vDNA. 3- To determine the impact of nuclear organization on integration site selection and on viral and host transcription. State of the art technologies will be applied to achieve these challenging objectives. If successful, this project will make an outstanding contributions not only to the field of HIV biology but also for the development of safe lentiviral vectors for gene therapy.

Host institution

CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
Net EU contribution
€ 2 500 000,00
Address
RUE MICHEL ANGE 3
75794 Paris
France

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Region
Ile-de-France Ile-de-France Paris
Activity type
Research Organisations
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Total cost
€ 2 500 000,00

Beneficiaries (1)