Genetic and chromatin regulation of Pvt1 monoallelic expression

While most genes are equivalently expressed on both alleles, genes with random monoallelic expression (RME) stably maintain expression from only one allele, but the mechanisms and consequences of RME remain unclear. We performed allele-specific RNA sequencing (RNA-seq) on ∼100 F<sub>1</sub> hybrid neural progenitor cell (NPC) clonal lines to reveal the extent of autosomal RME (aRME). Of the 287 aRME genes, Pvt1, an oncogenic long non-coding RNA, is an aRME with a genetic bias. In the absence of genetic differences, Pvt1 undergoes balanced aRME. Pvt1 monoallelic expression is maintained by allele-specific active and repressive histone modifications, opposed to DNA methylation. Additionally, we provide a two-step mechanism for the initiation of aRME and demonstrate that Pvt1 monoallelic expression results in a growth phenotype due to the interplay with Myc. These findings provide insight into how genetic differences can skew a stochastic process, resulting in monoallelic expression with a phenotypic consequence in early development.

Authors

Institutions

Publication Details

Journal
Cell Reports
Published
2025-11-01
DOI
https://doi.org/10.1016/j.celrep.2025.116554
Citations
1
Primary Topic
Genetic Syndromes and Imprinting
Type
article
Field-Weighted Citation Impact
1.82
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Genetic and chromatin regulation of Pvt1 monoallelic expression

Christy Luong, Édith Heard, Mason Chen, Howard Y. Chang et al.
1 citations
Cell Reports
Genetic Syndromes and Imprinting
1.82
article

Genetic and chromatin regulation of Pvt1 monoallelic expression

Christy Luong, Édith Heard, Mason Chen, Howard Y. Chang, Julia A. Belk, Katerina Kraft, Joanna Wysocka, Anne-Valérie Gendrel
article en
1 citations

Abstract

While most genes are equivalently expressed on both alleles, genes with random monoallelic expression (RME) stably maintain expression from only one allele, but the mechanisms and consequences of RME remain unclear. We performed allele-specific RNA sequencing (RNA-seq) on ∼100 F<sub>1</sub> hybrid neural progenitor cell (NPC) clonal lines to reveal the extent of autosomal RME (aRME). Of the 287 aRME genes, Pvt1, an oncogenic long non-coding RNA, is an aRME with a genetic bias. In the absence of genetic differences, Pvt1 undergoes balanced aRME. Pvt1 monoallelic expression is maintained by allele-specific active and repressive histone modifications, opposed to DNA methylation. Additionally, we provide a two-step mechanism for the initiation of aRME and demonstrate that Pvt1 monoallelic expression results in a growth phenotype due to the interplay with Myc. These findings provide insight into how genetic differences can skew a stochastic process, resulting in monoallelic expression with a phenotypic consequence in early development.

Cell ReportsVol. 44(11)
Stanford Medicine (US), European Molecular Biology Laboratory (DE), Instituto Gulbenkian de Ciência (PT), Stanford University (US)
Openalex Percentile: Top 11%
Genetic Syndromes and Imprinting
1.82
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Genetic and chromatin regulation of Pvt1 monoallelic expression — Christy Luong, Édith Heard, et al. · Cell Reports (2025) | TGRS Research Map | TGRS