Long terminal repeats influence deletion propensity and genome instability in proviruses across major retroviruses
- 1University of Zurich and University Hospital Zurich
Abstract
A hallmark of retroviral infection is integration of viral genomes into host chromosomes to form proviruses. Most proviruses are defective, particularly in people with HIV receiving antiretroviral therapy, with large internal deletions as a dominant outcome. The contribution of retroviral long terminal repeats (LTRs) in the formation of large internal deletions remains unclear. We used dual-fluorophore reporters based on HIV-1, HIV-2, and HTLV-1 LTRs, integrated at AAVS1 by CRISPR/Cas9, to test whether LTRs influence proviral integrity in the absence of reverse transcriptase or integrase. Cerulean expression was driven by the LTR and mCherry by an independent human promoter. Double-positive (Cerulean/mCherry) cells were a proxy for intact vectors, whereas single mCherry cells indicated latent and/or defective proviruses. Double-positive cells harboured intact vectors for all constructs. Non-inducible single mCherry populations were enriched for extensively deleted proviruses with HIV-1, HIV-2, or HTLV-1 LTRs, whereas the LTR-deficient reporter yielded few single mCherry cells, all with intact proviruses. The presence of LTRs was significantly associated with deleted genomes. HIV-1 and HTLV-1 showed higher observed deletion rates than HIV-2, but this was not statistically significant owing to limited sequence numbers. Single Cerulean populations across all constructs showed recurrent deletions affecting the mCherry cassette and upstream promoter, with short direct repeats at deletion junctions. These likely reflect microhomology-mediated end joining as a contributing repair mechanism during CRISPR/Cas9-mediated integration, in which LTRs may not directly contribute. Together, these data identify retroviral LTRs as contributors to the formation of large internal deletions in proviruses.
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BibTeX
@misc{bhattacharjee2026long,
title = {{Long terminal repeats influence deletion propensity and genome instability in proviruses across major retroviruses}},
author = {S. Bhattacharjee and K. Michalek and K. J. Metzner},
howpublished = {bioRxiv},
year = {2026},
month = oct,
doi = {10.64898/2026.10.12.758617},
url = {https://www.biorxiv.org/content/10.64898/2026.10.12.758617v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - Long terminal repeats influence deletion propensity and genome instability in proviruses across major retroviruses
AU - S. Bhattacharjee
AU - K. Michalek
AU - K. J. Metzner
PY - 2026
DA - 2026/10/12
PB - bioRxiv
DO - 10.64898/2026.10.12.758617
UR - https://www.biorxiv.org/content/10.64898/2026.10.12.758617v1
AB - A hallmark of retroviral infection is integration of viral genomes into host chromosomes to form proviruses. Most proviruses are defective, particularly in people with HIV receiving antiretroviral therapy, with large internal deletions as a dominant outcome. The contribution of retroviral long terminal repeats (LTRs) in the formation of large internal deletions remains unclear. We used dual-fluorophore reporters based on HIV-1, HIV-2, and HTLV-1 LTRs, integrated at AAVS1 by CRISPR/Cas9, to test whether LTRs influence proviral integrity in the absence of reverse transcriptase or integrase. Cerulean expression was driven by the LTR and mCherry by an independent human promoter. Double-positive (Cerulean/mCherry) cells were a proxy for intact vectors, whereas single mCherry cells indicated latent and/or defective proviruses. Double-positive cells harboured intact vectors for all constructs. Non-inducible single mCherry populations were enriched for extensively deleted proviruses with HIV-1, HIV-2, or HTLV-1 LTRs, whereas the LTR-deficient reporter yielded few single mCherry cells, all with intact proviruses. The presence of LTRs was significantly associated with deleted genomes. HIV-1 and HTLV-1 showed higher observed deletion rates than HIV-2, but this was not statistically significant owing to limited sequence numbers. Single Cerulean populations across all constructs showed recurrent deletions affecting the mCherry cassette and upstream promoter, with short direct repeats at deletion junctions. These likely reflect microhomology-mediated end joining as a contributing repair mechanism during CRISPR/Cas9-mediated integration, in which LTRs may not directly contribute. Together, these data identify retroviral LTRs as contributors to the formation of large internal deletions in proviruses.
ER -