Ectopic expression of the germline transcription factor LSL-1 contributes to developmental delay following failed maternal epigenetic reprogramming
- 1Kennesaw State University
Abstract
Proper transmission of cell identity between generations requires maternal epigenetic reprogramming mechanisms that prevent inappropriate inheritance of lineage-specific transcriptional programs. In Caenorhabditis elegans, loss of the H3K4me1/2 demethylase SPR-5 and the H3K9 methyltransferase MET-2 results in ectopic expression of germline genes in somatic tissues and severe developmental delay. Previous studies demonstrated that the chromatin regulator MES-4 contributes to these defects, but whether germline-specific transcription factors also participate in the ectopic transcriptional program remained unclear. Here, we investigated the role of the germline transcription factor LSL-1 in animals lacking SPR-5 and MET-2. We found that genes normally regulated by LSL-1 in the germline are significantly overrepresented among genes ectopically expressed in the soma of spr-5; met-2 progeny. Consistent with this observation, an endogenously tagged LSL-1 protein became ectopically expressed throughout somatic tissues when maternal SPR-5 and MET-2 activity was disrupted. Furthermore, depletion of LSL-1 partially suppressed the developmental delay observed in spr-5; met-2 mutants. Transcriptomic analyses revealed extensive overlap between MES-4- and LSL-1-dependent transcriptional programs, with most LSL-1-dependent genes also requiring MES-4. Notably, ectopic expression of lsl-1 itself depended on MES-4, suggesting that LSL-1 functions downstream of MES-4. Genes dependent on LSL-1 were strongly enriched for germline-associated expression programs and included previously identified direct LSL-1 targets. Together, our findings support a model in which MES-4 promotes ectopic expression of LSL-1, which in turn contributes to a shared germline-associated transcriptional program and developmental delay following failed maternal epigenetic reprogramming. These results demonstrate how lineage-restricted transcription factors cooperate with inherited chromatin states to reinforce aberrant transcriptional programs and disrupt cell fate boundaries.
Related
- Epigenetic reprogramming by promoter hypomethylation is linked to aberrant gene expression and transcriptomic plasticity in colorectal cancer
- Genome-wide comparative analysis of homeobox transcription factors in rice and expression profiles of selected genes reveal potential tissue and developmental stage specificity as well as abiotic stress responsiveness
- Generative design of functional disordered regions in a developmental transcription factor
- SIRPγ promotes CD8⁺ T cell exhaustion via metabolic-epigenetic reprogramming in tuberculous pleural effusion
- BORIS in Hormone-Driven Cancers: Epigenetic Reprogramming, Transcriptional Plasticity, and Therapeutic Implications
BibTeX
@misc{massenburg2026ectopic,
title = {{Ectopic expression of the germline transcription factor LSL-1 contributes to developmental delay following failed maternal epigenetic reprogramming}},
author = {Z. Massenburg and B. M. T. Nguyen and J. Labus and S. H. Johnson and S. D. Blancher and M. Jones and B. S. Carpenter},
howpublished = {bioRxiv},
year = {2026},
month = aug,
doi = {10.64898/2026.08.28.747910},
url = {https://www.biorxiv.org/content/10.64898/2026.08.28.747910v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - Ectopic expression of the germline transcription factor LSL-1 contributes to developmental delay following failed maternal epigenetic reprogramming
AU - Z. Massenburg
AU - B. M. T. Nguyen
AU - J. Labus
AU - S. H. Johnson
AU - S. D. Blancher
AU - M. Jones
AU - B. S. Carpenter
PY - 2026
DA - 2026/08/28
PB - bioRxiv
DO - 10.64898/2026.08.28.747910
UR - https://www.biorxiv.org/content/10.64898/2026.08.28.747910v1
AB - Proper transmission of cell identity between generations requires maternal epigenetic reprogramming mechanisms that prevent inappropriate inheritance of lineage-specific transcriptional programs. In Caenorhabditis elegans, loss of the H3K4me1/2 demethylase SPR-5 and the H3K9 methyltransferase MET-2 results in ectopic expression of germline genes in somatic tissues and severe developmental delay. Previous studies demonstrated that the chromatin regulator MES-4 contributes to these defects, but whether germline-specific transcription factors also participate in the ectopic transcriptional program remained unclear. Here, we investigated the role of the germline transcription factor LSL-1 in animals lacking SPR-5 and MET-2. We found that genes normally regulated by LSL-1 in the germline are significantly overrepresented among genes ectopically expressed in the soma of spr-5; met-2 progeny. Consistent with this observation, an endogenously tagged LSL-1 protein became ectopically expressed throughout somatic tissues when maternal SPR-5 and MET-2 activity was disrupted. Furthermore, depletion of LSL-1 partially suppressed the developmental delay observed in spr-5; met-2 mutants. Transcriptomic analyses revealed extensive overlap between MES-4- and LSL-1-dependent transcriptional programs, with most LSL-1-dependent genes also requiring MES-4. Notably, ectopic expression of lsl-1 itself depended on MES-4, suggesting that LSL-1 functions downstream of MES-4. Genes dependent on LSL-1 were strongly enriched for germline-associated expression programs and included previously identified direct LSL-1 targets. Together, our findings support a model in which MES-4 promotes ectopic expression of LSL-1, which in turn contributes to a shared germline-associated transcriptional program and developmental delay following failed maternal epigenetic reprogramming. These results demonstrate how lineage-restricted transcription factors cooperate with inherited chromatin states to reinforce aberrant transcriptional programs and disrupt cell fate boundaries.
ER -