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Interploidy hybridization between diploid and tetraploid has been an important approach to develop triploid hybrids in horticultural plants including citrus for seedless breeding. However, dysregulation of imprinted genes can lead to the failure of endosperm cellularization, resulting in abortion of triploid embryos before seed maturity, thereby impeding the efficiency of triploid generation. The identification of imprinted genes is essential for comprehending the impact of imprinting on endosperm cellularization and mitigating embryo abortion in interploidy hybridization. Herein, a genome-wide search for imprinted genes in citrus was performed using RNA sequencing of the endosperm collected from two pairs of reciprocal crosses and totally 296 imprinted genes were identified. Among them, the paternally imprinted genes (PEGs) showed a higher inclination toward endosperm-specific expression compared to maternally imprinted genes (MEGs), with a few demonstrating consistent imprinting across three developmental stages of endosperm and displaying homology with counterparts found in other plant species. The analysis of transposable element (TE) enrichment and DNA methylation revealed a significant enrichment of mutator TEs with higher level of DNA methylation around maternal imprinted genes, highlighting their vital role for controlling the expression of MEGs. By overexpressing the endosperm-specific expressed PEGs in Arabidopsis, we observed that the transgenic lines of OE-CsPEG1 exhibited an increased frequency of seed abortion, which appeared to be correlated with delayed endosperm cellularization, resembling the observed phenotypes in 2x × 4x interploidy hybridizations. Our research provides evidence supporting the functional conservation of imprinted genes in plants, thereby identifying potential targets for genetic improvement in triploid breeding.
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http://dx.doi.org/10.1111/tpj.70290 | DOI Listing |
Nucleic Acids Res
September 2025
Department of Genetics, University of Cambridge, Cambridge CB2 3EH, United Kingdom.
The mammary gland, which primarily develops postnatally, undergoes significant changes during pregnancy and lactation to facilitate milk production. Through the generation and analysis of 480 transcriptomes, we provide the most detailed allelic expression map of the mammary gland, cataloguing cell-type-specific expression from ex-vivo purified cell populations over 10 developmental stages, enabling comparative analysis. The work identifies genes involved in the mammary gland cycle, parental-origin-specific and genetic background-specific expression at cellular and temporal resolution, genes associated with human lactation disorders and breast cancer.
View Article and Find Full Text PDFStem Cell Rev Rep
September 2025
Stem Cells and Metabolism Research Program (STEMM), Research Programs Unit, Faculty of Medicine, University of Helsinki, Helsinki, 00014, Finland.
Mutations in Delta Like Non-Canonical Notch Ligand 1 (DLK1), a paternally expressed imprinted gene, underlie central precocious puberty (CPP), yet the mechanism remains unclear. To test the hypothesis that DLK1 plays a role in gonadotropin releasing hormone (GnRH) neuron ontogeny, 75 base pairs were deleted in both alleles of DLK1 exon 3 with CRISPR-Cas9 in human pluripotent stem cells (hPSCs). This line, exhibiting More than 80% loss of DLK1 protein, was differentiated into GnRH neurons by dual SMAD inhibition (dSMADi), FGF8 treatment and Notch inhibition, as previously described, however, it did not exhibit accelerated GNRH1 expression.
View Article and Find Full Text PDFIdentifying drivers of metastasis is essential for developing new treatments for patients with advanced disease. Here, we identify as a robust driver of breast cancer metastasis. Previous work established as an imprinted gene expressed by trophoblasts which are critical for vascular remodeling during placental development.
View Article and Find Full Text PDFAutosomal monoallelic gene expression and asynchronous replication between alleles are well-established features of imprinted genes and genes regulated by allelic exclusion. Inactivation/Stability Centers (I/SCs) are recently described autosomal loci that exhibit epigenetic regulation of allelic expression and replication timing, with differences that can be comparable to those observed between the active and inactive X chromosomes . Here we characterize hundreds of autosomal loci with allele-specific epigenetic regulation of replication timing and gene expression, defining them as I/SCs.
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