Search bioRxiv⌕ Search

Biology subjects

fan, j.

Publications and source records attributed to fan, j..

3 recordsLinked to original sources

Genomic Foundation Models Reveal Chromatin-Domain-Scale Transposable Element Impacts on Rice Genome Architecture

Alignment-based detection of transposable element (TE) insertion polymorphisms suffers from reference bias and multi-mapping errors in repetitive genomic regions, creating a fundamental validation bottleneck for population-scale structural variant catalogs. Here, we demonstrate that the OneGenome-Rice (OGR) genomic foundation model (GFM)--a 1.25 billion parameter Mixtral architecture trained on 422 rice genomes without TE annotations--provides an entirely orthogonal, alignment-free approach that resolves TE-mediated structural divergence at chromatin-domain resolution. At the CTB4a cold-tolerance locus on chromosome 4, OGR embeddings revealed that the aus subpopulation (NONA_BOKRA) carries 2.2-fold higher structural divergence from indica than japonica, consistent with its 728 subpopulation-exclusive cold-protective TE insertions. Sliding-window analysis across 4.4 megabases identified a 25.6-fold divergence enhancement at TE clusters relative to the conserved CTB4a gene body. Critically, the minimal effective resolution was established at approximately 20 kilobases--corresponding to the median size of topologically associating domains (TADs) in the rice genome--while individual TE sites at 500 base pairs were undetectable (P = 0.94). Non-neural baselines confirmed the signal derives from learned representations of genomic context rather than simple nucleotide statistics. These findings establish GFMs as orthogonal validation tools for population-scale TE genotyping and provide computational evidence that TE functional effects are organized at the chromatin-domain level, with direct implications for prioritizing functional TE variants in crop breeding.

plant biology↗

T2T Pangenome Reveals a 3.3kb Structural Variation Driving the De Novo Evolution of a Subspecies-Specific NLR Gene in Rice

BackgroundThe genomic region spanning 1.1-1.3 Mb on rice chromosome 6 is a recognized structural variation (SV) hotspot linked to Rice Black-Streaked Dwarf Virus (RBSDV) resistance. However, the precise molecular mechanism has remained elusive due to the inherent "reference bias" of the japonica-based genome, which lacks the critical causative sequences. MethodsLeveraging a neuro-symbolic-driven analysis of gap-free Telomere-to-Telomere (T2T) pangenome datasets and the LGEMP engine, we conducted a high-resolution comparative study between indica (9311) and japonica (Nippon bare). This approach allowed us to treat genomic variations as 3D structural building blocks rather than linear strings. ResultsWe identified a 3.3 kb large-scale insertion uniquely present at the 1.21 Mb locus in 9311. This SV, likely mediated by transposable elements, exhibits extreme sequence divergence (24% identity). We demonstrate that this insertion acts as a topological modifier, driving a dramatic functional shift: while the japonica allele encodes a basic DUF590 transporter, the indica allele has undergone de novo evolution into a complete CC-NBS-LRR (NLR) immune receptor. Transcriptomic profiling confirmed the generation of six novel isoforms (T01-T06) enabled by the SVs structural re-organization. Validation across 16 representative T2T assemblies confirms this 3.3 kb SV as an indica-specific "evolutionary patch," effectively filling the "missing heritability" gap in rice viral immunity. ConclusionOur findings uncover a novel mechanism of gene birth through structural re-organization at high-diversity hotspots. By integrating T2T pangenomics with AI-driven inference, this study provides a definitive molecular marker for the precision breeding of virus-resistant crops and redefines our understanding of subspecies-specific adaptation..

genetics↗

IDOL deficiency inhibits cholesterol-rich diet-induced atherosclerosis in rabbits

BACKGROUNDThe E3 ubiquitin ligase IDOL (Inducible Degrader of the LDL-Receptor) contributes to regulation of cholesterol metabolism through degradation of LDLR, VLDLR and ApoER2. Human genetic studies support the hypothesis that IDOL could serve as a target for the treatment of dyslipidemia. However, species-specific differences in overall lipid metabolism and IDOL regulation require new preclinical models to realize its therapeutic potential. We leveraged the advantages afforded by the rabbit model to address those limitations and generated a novel rabbit IDOL knockout, which we characterized in the context of atherosclerosis. METHODSIDOL-/- rabbits were generated by CRISPR/Cas9 technology. IDOL-/- and wildtype littermates, on standard (SD) and atherogenic high-cholesterol diets (HCDs) were compared through assessment of lipid and lipoprotein profiles, triglyceride clearance, lipoprotein lipase (LPL) activity, liver pathology, atherosclerosis development, and fecal cholesterol, with bile acid contents assessed by mass spectrometry. ResultsHepatic IDOL expression was increased in response to hypercholesterolemia and hypertriglyceridemia induced by HCD. On SD, loss of IDOL increased LDLR stability with reduced total cholesterol in plasma. On HCD, IDOL-/- rabbits showed simultaneous and remarkable reduction in hypercholesterolemia and hypertriglyceridemia associated with enhanced lipid clearance and LPL activity as well as increased bile acid excretion in feces. IDOL-/- rabbits presented markedly reduced HCD-induced atherosclerosis in the aorta and left coronary artery, without enhanced liver steatosis. CONCLUSIONSLoss of IDOL in rabbits recapitulates human genetic findings, thus setting the stage to accelerate preclinical studies towards development of strategies targeting IDOL for the treatment of atherosclerotic cardiovascular disease.

physiology↗