Acute LINE-1 overexpression rewires the transcriptome, proteome and secretome of primary human fibroblasts
- 1University of Southern California
Abstract
A large portion of eukaryotic genomes is composed of transposable elements, which are usually kept repressed in young, healthy cells but can be derepressed in response to cell senescence and organismal aging. LINE-1 (L1) is the most abundant TE in the human genome by percent coverage, and its derepression has been implicated in inflammaging responses. However, whether L1 transcription itself is sufficient to drive aging-associated molecular phenotypes in healthy cells has not been extensively explored. Here, we leverage a multi-omic approach combining transcriptomics, proteomics, and secretomics of primary human IMR-90 fibroblasts transiently overexpressing a human L1Hs element in order to define the systems-level consequences of L1 transcription. Intriguingly, transient L1Hs overexpression induced widespread remodeling of the transcriptome, proteome and secretome, impacting pathways related to cell cycle regulation and interferon signaling. Interrogation of multiple independent L1 elements revealed both shared and distinct cellular responses to acute expression. Thus, our findings demonstrate that acute L1 expression induces coordinated molecular remodeling extending beyond canonical retrotransposition-associated pathways, rather than simply mimicking senescence or triggering antiviral signaling. This study establishes a comprehensive multi-omics resource for investigating the impact of L1 transcription in human cells and highlights the need to consider individual transposable element families as distinct regulators of cellular state during aging and disease.
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BibTeX
@misc{bravo2026acute,
title = {{Acute LINE-1 overexpression rewires the transcriptome, proteome and secretome of primary human fibroblasts}},
author = {J. I. Bravo and E. Tewelde and C. D. King and N. S. Tellakula and B. Schilling and B. A. Benayoun},
howpublished = {bioRxiv},
year = {2026},
month = sep,
doi = {10.64898/2026.09.03.749265},
url = {https://www.biorxiv.org/content/10.64898/2026.09.03.749265v1},
note = {CC BY-NC-ND},
}
RIS
TY - UNPB
TI - Acute LINE-1 overexpression rewires the transcriptome, proteome and secretome of primary human fibroblasts
AU - J. I. Bravo
AU - E. Tewelde
AU - C. D. King
AU - N. S. Tellakula
AU - B. Schilling
AU - B. A. Benayoun
PY - 2026
DA - 2026/09/03
PB - bioRxiv
DO - 10.64898/2026.09.03.749265
UR - https://www.biorxiv.org/content/10.64898/2026.09.03.749265v1
AB - A large portion of eukaryotic genomes is composed of transposable elements, which are usually kept repressed in young, healthy cells but can be derepressed in response to cell senescence and organismal aging. LINE-1 (L1) is the most abundant TE in the human genome by percent coverage, and its derepression has been implicated in inflammaging responses. However, whether L1 transcription itself is sufficient to drive aging-associated molecular phenotypes in healthy cells has not been extensively explored. Here, we leverage a multi-omic approach combining transcriptomics, proteomics, and secretomics of primary human IMR-90 fibroblasts transiently overexpressing a human L1Hs element in order to define the systems-level consequences of L1 transcription. Intriguingly, transient L1Hs overexpression induced widespread remodeling of the transcriptome, proteome and secretome, impacting pathways related to cell cycle regulation and interferon signaling. Interrogation of multiple independent L1 elements revealed both shared and distinct cellular responses to acute expression. Thus, our findings demonstrate that acute L1 expression induces coordinated molecular remodeling extending beyond canonical retrotransposition-associated pathways, rather than simply mimicking senescence or triggering antiviral signaling. This study establishes a comprehensive multi-omics resource for investigating the impact of L1 transcription in human cells and highlights the need to consider individual transposable element families as distinct regulators of cellular state during aging and disease.
ER -