Hongwei Zhou | Search PubMed

PubMed2025

Genome-wide association study to dissect the genetic architecture of bolting-related traits in carrot (Daucus carota).

As a crucial root vegetable, the phenomenon of bolting and flowering presents a significant challenge to the commercial value of carrot. However, the genetic mechanism of carrot bolting remains to be fully elucidated. In this study, we conducted a two-year cultivation experiment with a population of 240 carrots to examine traits associated with bolting. We conducted whole-genome sequencing on these carrots and subsequently performed population structure analysis, as well as genome-wide association studies (GWAS). A total of nine single nucleotide polymorphism (SNP) loci were identified across diverse environmental conditions that exhibited significant associations with bolting speed and other traits. Furthermore, within 93 candidate genes identified, the RING-domain zinc-finger protein LOC108205243 was determined to play a significant role in the regulation of bolting traits. The SNPs and candidate genes identified in this research may serve as molecular markers for bolting traits, thereby offering essential resources for genetic engineering breeding efforts aimed at managing bolting in carrots.

Daucus carota↗

PubMed2025

Mapping early PRC2 nucleation sites upon Suz12 reintroduction reveals features of de novo Polycomb recruitment.

Polycomb domains safeguard cell identity by maintaining lineage-specific chromatin states enriched in repressive histone modifications, preserving the epigenetic memory of cell lineages. While Polycomb Repressive Complex 2 (PRC2) can re-establish its occupancy after perturbation, the mechanisms that guide de novo Polycomb recruitment remain unclear. To address this, we engineered an auxin-inducible degradation system to reversibly deplete and reintroduce the endogenous PRC2 core subunit Suz12 in mouse embryonic stem cells (mESCs). Genome-wide profiling at an early recovery time point revealed ~1,100 PRC2 nucleation sites, characterized by rapid Suz12 and histone H3K27me3 re-accumulation with strong signal, with minimal impact on gene expression. These sites were significantly enriched at bivalent promoters, coinciding with unmethylated CpG islands and chromatin states associated with developmental regulation, and were largely conserved in differentiated cells. Motif analysis identified G/C-rich DNA sequences associated with E2F and zinc-finger proteins, alongside strong co-occupancy with MTF2 and JARID2, two PRC2 cofactors previously implicated in Polycomb targeting. Notably, a subset of nucleation sites overlapped with long-range chromatin interaction anchors in histone H3K27me3 HiChIP datasets. These findings reveal that PRC2 de novo nucleation sites are associated with a combination of chromatin states, DNA sequence features, cofactor co-occupancy and spatial genome organization, suggesting that epigenetic memory can be re-established through defined genomic and chromatin features.

Epigenetic memory↗