LINE-1 retrotransposons mediate cis-acting transcriptional control in human pluripotent stem cells and regulate early brain development

Long interspersed nuclear element 1 (L1) retrotransposons represent a vast source of genetic variability. However, mechanistic analysis of whether and how L1s contribute to human developmental programs is lacking, in part due to the challenges associated with specific profiling and manipulation of human L1 expression. Here, we show that thousands of hominoid-specific L1 integrants are expressed in human induced pluripotent stem cells and cerebral organoids. The activity levels of individual L1 promoters vary widely and correlate with an active epigenetic state. Efficient on-target CRISPR interference (CRISPRi) silencing of L1s revealed nearly a hundred co-opted L1-derived chimeric transcripts, and L1 silencing resulted in changes in neural differentiation programs and reduced cerebral organoid size. Together, these data implicate L1s and L1-derived transcripts in hominoid-specific CNS developmental processes.

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Publication Details

Journal
Cell Genomics
Published
2025-08-22
DOI
https://doi.org/10.1016/j.xgen.2025.100979
Citations
5
Primary Topic
Chromosomal and Genetic Variations
Type
article
Field-Weighted Citation Impact
8.75
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article

LINE-1 retrotransposons mediate cis-acting transcriptional control in human pluripotent stem cells and regulate early brain development

Fereshteh Dorazehi, Johan Jakobsson, Molly Hammell, Diahann A. M. Atacho et al.
5 citations
Cell Genomics
Chromosomal and Genetic Variations
8.75
article

LINE-1 retrotransposons mediate cis-acting transcriptional control in human pluripotent stem cells and regulate early brain development

Fereshteh Dorazehi, Johan Jakobsson, Molly Hammell, Diahann A. M. Atacho, Patricia Gerdes, Symela Koutounidou, Pia A. Johansson, Raquel Garza, Yogita Sharma, Laura Castilla‐Vallmanya, Oliver H. Tam, Christopher H. Douse, Anita Adami, Agnete Kirkeby, Roger A. Barker, Jonas Johansson
article en
5 citations

Abstract

Long interspersed nuclear element 1 (L1) retrotransposons represent a vast source of genetic variability. However, mechanistic analysis of whether and how L1s contribute to human developmental programs is lacking, in part due to the challenges associated with specific profiling and manipulation of human L1 expression. Here, we show that thousands of hominoid-specific L1 integrants are expressed in human induced pluripotent stem cells and cerebral organoids. The activity levels of individual L1 promoters vary widely and correlate with an active epigenetic state. Efficient on-target CRISPR interference (CRISPRi) silencing of L1s revealed nearly a hundred co-opted L1-derived chimeric transcripts, and L1 silencing resulted in changes in neural differentiation programs and reduced cerebral organoid size. Together, these data implicate L1s and L1-derived transcripts in hominoid-specific CNS developmental processes.

Cell GenomicsVol. 5(10)
Lund University (SE), Wellcome/MRC Cambridge Stem Cell Institute (GB), Novo Nordisk Foundation (DK), Research Network (United States) (US)
Zero hunger
Openalex Percentile: Top 3%
Chromosomal and Genetic Variations
8.75
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