← Literature list

Polycomb-mediated repression of paternal chromosomes maintains haploid dosage in diploid embryos of Marchantia.

Montgomery, S. A., et al. · 2022 · eLife   research

doi:10.7554/elife.79258   PMID:35996955   PMC9402228

Linked genes (8)  4 core 4 peripheral

Gene ID Name Evidence / Role Function (this paper)
Mp5g17740 MpE(z)2 experimental subject PRC2 catalytic subunit; CRISPR/Cas9 dual knockout with MpE(z)3 in females, profiled by transcriptome and CUT&RUN. Maternal inheritance is essential for paternal H3K27me3 deposition. Loss reduces H3K27me3, reactivates paternal genes, drops embryo survival to ~20% and abolishes viable spores.
Mp5g22900 MpE(z)3 experimental subject PRC2 catalytic subunit; CRISPR/Cas9 dual knockout with MpE(z)2 in females, profiled by transcriptome and CUT&RUN. Maternal copy required for paternal chromosome H3K27me3; combined loss impairs imprinting, reactivates paternal alleles and causes embryonic lethality.
MpEz2 missing experimental subject E(z)/EZH Polycomb subunit; targeted (CRISPR) in paternal-chromosome H3K27me3 repression.
MpEz3 missing experimental subject E(z)/EZH Polycomb subunit; CRISPR target in Polycomb-mediated repression.
Mp5g18040 MpE(z)1 experimental comparator Expressed in all tissues including embryos; not functionally knocked out due to haploid lethality, so likely accounts for residual H3K27me3 in e(z)2/e(z)3 mutants, indicating redundancy among PRC2 catalytic subunits.
Mp3g06080 MpFIE experimental background Non-catalytic PRC2 subunit; expression profiling only, expressed across developmental stages, supporting a functional Polycomb complex in Marchantia.
MpMSI1 missing experimental background Non-catalytic PRC2 subunit; expression profiling only, constitutively expressed, completing the Marchantia PRC2 complex composition.
MpSu(z)12 missing experimental background Non-catalytic PRC2 subunit; expression profiling only, constitutively expressed, contributing to PRC2 subunit composition.