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Biology subjects

William, M.

Publications and source records attributed to William, M..

2 recordsLinked to original sources

Genetic Diversity and Population Structure of Maize Doubled Haploid Lines from Drought and Low Nitrogen Tolerant Populations

Understanding the genetic diversity and population structure of breeding materials is essential for developing stress-resilient cultivars. In tropical maize, where drought and low soil nitrogen (low N) severely limit productivity, continuous development of tolerant varieties remains a priority. This study assessed the genetic diversity and population structure of 250 doubled haploid lines (DHLs) derived from five drought- and low N-tolerant tropical populations. Genotyping was performed using mid-density DArTseq markers, yielding 3,305 high-quality SNPs for analysis. Results revealed a moderate level of diversity among the DHLs, with an average genetic distance of 0.39, a polymorphism information content (PIC) of 0.33, and a minor allele frequency (MAF) of 0.29. These values reflect substantial allelic variation, important for identifying complementary parental combinations in hybrid development. Discriminant analysis of principal components (DAPC) grouped the DHLs into five distinct clusters, largely corresponding to their source populations, although some admixture was observed. This indicates that while the genetic backgrounds of the source populations were mostly retained, recombination introduced useful variation. Overall, the clear population structure and high diversity observed among these DHLs provide a strong genetic foundation for future maize improvement. These lines represent valuable resources for heterotic group formation, hybrid development, and recurrent selection schemes aimed at enhancing drought and low nitrogen tolerance in tropical maize.

genetics↗

Modulating Mesenchymal Stromal Cell Microenvironment Alters Exosome RNA Content and Ligament Healing Capacity

Although mesenchymal stromal cell (MSC) based therapies hold promise in regenerative medicine, their applications in clinical settings remain challenging due to issues such as immunocompatibility and cell stability. MSC-derived exosomes, small vesicles carrying various bioactive molecules, are a promising cell-free therapy to promote tissue regeneration. However, it remains unknown mainly regarding the ability to customize the content of MSC-derived exosomes, how alterations in the MSC microenvironment influence exosome content, and the effects of such modifications on healing efficiency and mechanical properties in tissue regeneration. In this study, we used an in vitro system of human MSC-derived exosomes and an in vivo rat ligament injury model to address these questions. We found a context-dependent correlation between exosomal and parent cell RNA content. Under native conditions, the correlation was moderate but heightened with microenvironmental changes. In vivo rat ligament injury model showed that MSC-derived exosomes increased ligament max load and stiffness. We also found that changes in the MSCs microenvironment significantly influence the mechanical properties driven by exosome treatment. Additionally, a link was identified between altered exosomal microRNA levels and expression changes in microRNA targets in ligaments. These findings elucidate the nuanced interplay between MSCs, their exosomes, and tissue regeneration. Graphic Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=94 SRC="FIGDIR/small/563485v2_ufig1.gif" ALT="Figure 1"> View larger version (27K): org.highwire.dtl.DTLVardef@2b45bborg.highwire.dtl.DTLVardef@ef2222org.highwire.dtl.DTLVardef@1a9f1f1org.highwire.dtl.DTLVardef@4b1ca2_HPS_FORMAT_FIGEXP M_FIG C_FIG

cell biology↗