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Abbas, Z.

Publications and source records attributed to Abbas, Z..

2 recordsLinked to original sources

Dissecting the genetic basis of DUS characters in Pakistani wheat varieties

Distinctness, Uniformity and Stability (DUS) testing is fundamental to varietal characterization and the protection of Plant Breeders Rights (PBRs), but conventional DUS assessment relies predominantly on morphological characteristics whose expression may be influenced by environmental conditions, developmental stage and observer-related variation. Integrating character-specific molecular markers with conventional DUS assessment may therefore improve the reproducibility and genetic resolution of varietal identification. This study investigated the genetic architecture of DUS characteristics in a panel of 102 historical and modern Pakistani wheat varieties using genome-wide association studies (GWAS). Phenotypic variation was evaluated using distribution, correlation and hierarchical clustering analyses, while the germplasm was genotyped using a wheat genotyping-by-targeted sequencing platform. After quality filtering, 21,670 high-quality single-nucleotide polymorphisms (SNPs) were retained for analyses of genetic diversity, population structure, linkage disequilibrium (LD) and marker-trait associations. Population structure analysis indicated extensive admixture, with cross-entropy supporting K = 9 ancestral components, whereas hierarchical genetic clustering separated the germplasm into five broad groups. The first three principal components explained 8.09%, 7.20% and 5.39% of the total genetic variation, respectively. GWAS using BLINK and FarmCPU identified significant associations for several diagnostically important DUS characteristics. Growth habit was strongly associated with SNP 1B_129176704, with an additional signal on chromosome 5B. Shattering showed its strongest association at 1D_445256324, accompanied by several closely linked SNPs in the same region and a secondary significant locus at 7B_703502819. Flag leaf length was associated with a cluster of SNPs on chromosome 6A, while tiller density showed a major association with 5D_205488820. These findings demonstrate substantial phenotypic and genetic diversity within Pakistani wheat germplasm and identify genomic regions that merit validation as character-specific molecular tools to complement conventional DUS testing and PBR implementation.

plant biology↗

Age-dependent tumor-immune interactions underlie immunotherapy response in pediatric cancer

Pediatric cancers originate in rapidly growing tissues within the context of a developing host. However, the interactions between cancer cells and the developing immune system are incompletely understood. Here, we established a suite of pediatric syngeneic mouse cancer models across diverse anatomical sites and compared their tumor immune microenvironment with that in adult mice. Tumors in pediatric mice exhibited significantly accelerated growth and diminished leukocyte infiltration, dominated by naive-like PD-1low/CD8+ T cells, and proliferative MHCIIlow/PD-L1hi/CD86low macrophages. Tumor-infiltrating leukocytes in pediatric mice were enriched for MYC targets, which was also observed in pediatric patient samples. Furthermore, pediatric mice displayed poor responses to anti-PD-1/PD-L1 or bispecific T cell engager antibodies, which could be reversed by inducing a proinflammatory microenvironment via MYC inhibition or inducing macrophage polarization to an MHCIIhi phenotype. These findings underscore the significant influence of young age on cancer immune responses and reveal potential new therapeutic opportunities for pediatric cancers. HIGHLIGHTSO_LIAllograft tumors exhibit markedly accelerated growth in pediatric hosts compared to adults. C_LIO_LITumors growing in pediatric mice have reduced leukocyte infiltration, dominated by naive-like PD-1low/CD8+ T cells, and MHCIIlow/M2-like macrophages. C_LIO_LIEnrichment of MYC target genes is observed in pediatric mouse tumors and confirmed in primary patient tumor samples. C_LIO_LIPediatric mice display reduced response to anti-PD-1/PD-L1 and BiTE immunotherapy, which can be reversed by remodeling the TIME, using either MYC inhibition or macrophage polarization. C_LI

cancer biology↗