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Biology subjects

Berton, M.

Publications and source records attributed to Berton, M..

2 recordsLinked to original sources

Identification of heterotic group-specific haplotypes and impact of residual inbreeding on grain yield of maize elite hybrids

Modern hybrid maize (Zea mays L.) breeding programs are based on the management of distinct complementary heterotic groups to maximize heterosis in high-performing hybrids. This practice lowers shared genetic segments and increases divergence between groups to limit inbreeding in hybrids. However, most breeding programs have not always enforced strict separation between heterotic groups in the past. Competitor commercial hybrids were notably a common elite germplasm source for inbred development, which would diminish divergence between groups. This study proposes a new haplotype-based approach to assess hybrids residual inbreeding based on parental similarity. The new haplotype method has a stronger significant negative effect on hybrids grain yield than raw SNP data. Evaluation of modern experimental hybrids uncovered related inbreds contributing to superior rates of residual inbreeding. Analysis of these inbreds revealed haplotype transfers between heterotic groups, originating notably from the use of a Stiff Stalk-Iodent commercial hybrid as breeding starts material in both Stiff Stalk and Non-Stiff Stalk breeding populations. The introduction of this intergroup parent generated heterotic-group-specific haplotype migration between crossing pools. These fragments caused significant genome-wide residual inbreeding in experimental hybrids across selection cycles. This study highlights the necessity for accurate evaluation of external sources of diversity to minimize haplotype transfers and admixture between crossing pools. We demonstrate the consequences of using commercial hybrids in inbred development, particularly regarding residual inbreeding, and their effects on hybrid performance. Insights from these results can assist breeders in optimizing the choice of parents for introducing genetic diversity in a reciprocal recurrent selection scheme. KEY MESSAGEHaplotype-based hybrids parental similarity better predicts grain yield than marker-based identity-by-state. Utilization of commercial hybrids as breeding start material resulted in higher hybrid residual inbreeding even after several selection cycles

genetics↗

A Developmental Lectin-Glycan Program Enables Early Breast Cancer Dissemination and Metastatic Onset

Early dissemination of breast cancer cells can precede clinically detectable tumor progression, yet the programs enabling this process, remain poorly understood. Here, we identify a developmental glycocheckpoint governed by the galectin-1 (GAL1)-glycan axis that is hijacked during early breast cancer dissemination. In the mammary gland, regulated GAL1 expression and glycan accessibility directed epithelial lineage specification and progesterone-induced branching morphogenesis. This program was aberrantly reactivated in early breast cancer lesions to promote epithelial plasticity, stem-like traits and metastatic competence. Mechanistically, GAL1 was enriched in mammary stem cell compartments and sustained progesterone receptor expression and activity. Genetic ablation or therapeutic inhibition of GAL1 across breast cancer models restrained early lesion progression, reduced circulating tumor cell frequency, and limited lung metastasis. Consistent with these findings, high GAL1 expression combined with low expression of the GAL1-restricting sialyltransferase ST6GAL1 was associated with poor clinical outcomes in patients. Thus, breast cancer co-opts a developmental GAL1-glycan program to disseminate early, revealing an unexpected link between mammary morphogenesis and metastatic progression and identifying GAL1 as a therapeutic vulnerability in early-stage disease.

cancer biology↗