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During early vertebrate embryogenesis, maternal Wnt/β-catenin signaling is thought to locally initiate expression of dorsal-specific genes. Here, and were identified as important maternal and zygotic modulators of Wnt signaling to initiate and specify ventral genes. Expression of ventral , , and was all obviously enhanced in either maternal or zygotic morphants, and in both heterozygous and homozygous mutants, but their expression was suppressed in embryos with over-expression of . Additionally, were revealed to suppress ventral fates in embryos Wnt/β-catenin1/Tcf signaling, complimentary to their roles in suppressing dorsal fates Wnt/β-catenin2 signaling. Moreover, were also revealed to obviously suppress the expression of induced by β-catenin2 rather than by β-catenin1, and the dorsal expression of in embryos was obviously suppressed by ectopic expression of . This study uncovers a novel dorsal-ventral patterning pathway, with and inhibiting ventral cells suppressing Wnt/β-catenin1/Tcf signaling and inducing dorsal cells indirectly suppressing β-catenin2-induced on the dorsal side of embryos.
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http://dx.doi.org/10.7150/ijbs.18997 | DOI Listing |
Zool Res
September 2025
MOE Key Laboratory of Marine Genetics and Breeding, College of Marine Life Sciences, Ocean University of China, Qingdao, Shandong 266003, China.
Bivalve mollusks represent a taxonomically and economically significant clade within Mollusca. However, the regulatory mechanisms governing their embryonic development remain poorly characterized. The dwarf surf clam ( ), characterized by a short generation time and high fecundity, has recently gained recognition as an ideal model system for bivalve embryological research.
View Article and Find Full Text PDFMedComm (2020)
September 2025
Department of Laboratory Medicine Zhongnan Hospital of Wuhan University Wuhan China.
RNA modifications, including N6-methyladenosine (m6A), 5-methylcytosine, and pseudouridine, serve as pivotal regulators of gene expression with significant implications for human health and disease. These dynamic modifications influence RNA stability, splicing, translation, and interactions, thereby orchestrating critical biological processes such as embryonic development, immune response, and cellular homeostasis. Dysregulation of RNA modifications is closely associated with a variety of pathologies.
View Article and Find Full Text PDFEMBO Rep
September 2025
School of Biological and Behavioural Sciences, Queen Mary University of London, Mile End Road, E1 4NS, London, UK.
Early animal development can be remarkably variable, influenced by lineage-specific reproductive strategies and adaptations. Yet, early embryogenesis is also strikingly conserved in certain groups, such as Spiralia. In this clade, a shared cleavage program (i.
View Article and Find Full Text PDFDev Cell
August 2025
Friedrich Miescher Institute for Biomedical Research, 4056 Basel, Switzerland; Faculty of Sciences, University of Basel, 4056 Basel, Switzerland. Electronic address:
Except for regulatory CpG-island sequences, genomes of most mammalian cells are widely DNA-methylated. In oocytes, though, DNA methylation (DNAme) is largely confined to transcribed regions. The mechanisms restricting de novo DNAme in oocytes and their relevance thereof for zygotic genome activation and embryonic development are largely unknown.
View Article and Find Full Text PDFNucleic Acids Res
August 2025
Institute of Molecular Biology, Academia Sinica, Taipei 11529, Taiwan.
Rad51 and meiosis-specific Dmc1 catalyze homologous recombination (HR) between maternal and paternal chromosomes during meiosis in many sexual eukaryotes, generating three interhomolog (IH) recombination products: non-crossovers (NCOs), class I interference-sensitive crossovers (COs), and class II non-interfering COs. CO interference suppresses relatively close CO formation. Some COs form chiasmata, which physically connect homologous chromosomes and ensure proper chromosome segregation during meiosis I.
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