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Biology subjects

Tasaki, M.

Publications and source records attributed to Tasaki, M..

2 recordsLinked to original sources

Efficient genomic prediction at reduced training size and moderate marker density in an expanded aus-NAM population of rice

Genomic selection (GS) can accelerate genetic gain in crops, but its effectiveness depends on training population design and marker density. Nested association mapping (NAM) populations provide a structured framework that captures broad allelic diversity within a controlled genetic background. Here, we evaluated genomic prediction (GP) and genome-wide association study (GWAS) performance in an expanded aus-NAM population of rice comprising 1,818 recombinant inbred lines across 14 families and 11 agronomic traits, using genotyping-by-sequencing (GBS) markers and projected whole-genome sequence variants. Prediction accuracy plateaued at moderate marker densities ([~]20k SNPs) and with training populations of [~]500 lines ([~]40-60% of the available pool), with trait heritability emerging as the strongest determinant of predictive performance rather than model choice or marker density. In contrast, GWAS resolution continued to improve with increasing marker density, enabling detection of additional loci, including a chromosome 12 locus associated with heading date, while consistently recovering well-characterized genes such as EARLY HEADING DATE 1 (Ehd1) and SEMIDWARF 1 (SD1). These contrasting patterns indicate that GP reaches near-optimal performance once genome-wide variation is adequately represented, whereas GWAS benefits from higher marker density through improved locus resolution. The present study establishes a benchmark for implementing breeding programs involving japonica/indica crosses using GP in a single environment.

plant biology↗

Cryo-EM structure of cardiac amyloid fibrils from an immunoglobulin light chain (AL) amyloidosis patient

Systemic light chain (AL) amyloidosis is a life-threatening disease caused by aggregation and deposition of monoclonal immunoglobulin light chains (LC) in target organs. Severity of heart involvement is the most important factor determining prognosis. Here, we report the 4.0 [A] resolution cryo-electron microscopy (cryo-EM) map and structural model of amyloid fibrils extracted from the heart of an AL patient affected by severe amyloid cardiomyopathy. The fibrils are composed of one asymmetric protofilament, showing typical 4.9 [A] stacking and parallel cross-{beta} architecture. Two distinct polypeptide stretches belonging to the LC variable domain (Vl) could be modelled in the density (total of 77 residues), stressing the role of the Vl domain in fibril assembly and LC aggregation. Despite high levels of Vl sequence variability, residues stabilising the observed fibril core are conserved through several Vl domains, highlighting structural motifs that may be common to misfolded LCs. Our data shed first light on the architecture of life-threatening LC amyloid deposits, and provide a rationale for correlating LC amino acid sequences and fibril structures.

biochemistry↗