Search bioRxiv⌕ Search

bioRxiv · 10.1101/287474

Whole-exome sequencing identified rare variants associated with body length and girth in cattle

Abstract

Body measurements can be used in determining body size to monitor the cattle growth and examine the response to selection. Despite efforts putting into the identification of common genetic variants, the mechanism understanding of the rare variation in complex traits about body size and growth remains limited. Here, we firstly performed GWAS study for body measurement traits in Simmental cattle, however there were no SNPs exceeding significant level associated with body measurements. To further investigate the mechanism of growth traits in beef cattle, we conducted whole exome analysis of 20 cattle with phenotypic differences on body girth and length, representing the first systematic exploration of rare variants on body measurements in cattle. By carrying out a three-phase process of the variant calling and filtering, a sum of 1158, 1151, 1267, and 1303 rare variants were identified in four phenotypic groups of two growth traits, higher/ lower body girth (BG_H and BG_L) and higher/lower body length (BL_H and BL_L) respectively. The subsequent functional enrichment analysis revealed that these rare variants distributed in 886 genes associated with collagen formation and organelle organization, indicating the importance of collagen formation and organelle organization for body size growth in cattle. The integrative network construction distinguished 62 and 66 genes with different co-expression patterns associated with higher and lower phenotypic groups of body measurements respectively, and the two sub-networks were distinct. Gene ontology and pathway annotation further showed that all shared genes in phenotypic differences participate in many biological processes related to the growth and development of the organism. Together, these findings provide a deep insight into rare genetic variants of growth traits in cattle and this will have a promising application in animal breeding.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Chen, Y., Du, M., Liu, Y., Gao, X., Zhang, W., Xu, L., Zhang, L., Lingyang, X., Gao, H., Bo, Z., Zhao, M., Li, J.. 2018-03-23. Whole-exome sequencing identified rare variants associated with body length and girth in cattle. https://doi.org/10.1101/287474

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Mapping, stacking and characterization of a novel resistance haplotype against GpaVvrn-virulent Globodera pallida derived from wild potato relative Solanum brevicaule

Potato production is threatened by pests and pathogens. Among the most harmful are the potato cyst nematodes (PCN), including Globodera pallida. The major control measures are potato cultivars harbouring resistance genes. However, virulent nematode populations are breaking through the most broadly applied resistance genes, and therefore novel resistance genes are required to keep control of G. pallida. In this study we map a resistance locus in wild potato relative Solanum brevicaule to the bottom of chromosome 11 (42.83 - 42.85 Mb) using a k-mer based bulked segregant analysis and name the resistant haplotype GpaXIbrc. The presence of the GpaXIbrc marker in the potato genome significantly increases resistance against a GpaVvrn-virulent G. pallida population (AMPOP01). Furthermore, the GpaXIbrc haplotype was stacked with three other resistance haplotypes: GpaXItar, GpaVvrn, and GpaIXvrn. Stacking of the novel GpaXIbrc haplotype to these other resistance haplotypes resulted in a significant increase in resistance. The largest effect was seen in combinations with 'major' resistance haplotypes GpaVvrn + GpaIXvrn and GpaXItar + GpaXIbrc. To determine whether we are dealing with a novel allele, the resistance mechanism underlying the GpaXIbrc haplotype was described after performing an in vitro bioassay. The resistance mechanism was different from GpaXIspl as described in literature, which is also localized at the bottom of chromosome 11. Therefore, we conclude that we found a novel resistance allele originating from S. brevicaule.

genetics↗

Cellular context shapes the transcriptomic impact of somatic variants

Somatic SNVs are commonly prioritized by recurrence or sequence annotation, leaving the molecular consequences of private variants unresolved. We developed PrismSNV and Ligo-Seq, a single-cell full-length transcriptome sequencing platform, to quantify transcriptomic displacement associated with within-cell SNV-state toggling. Across 26 samples from three cancer types, more than 60% of candidate SNVs showed significant cell-type-specific displacement with over 30% variation in magnitude. Sequence-based deleteriousness was poorly aligned with cellular displacement, and fewer than 3% of top-displacement SNVs across six tumor types were catalogued in ClinVar. Displacement was strongest in transcriptionally plastic, less differentiated states. Analysis of 655,349 CD4+ T-cell transcriptomes further showed that SNV-gene associations changed in magnitude and sometimes direction during activation. Lack of recurrence or clinical annotation does not imply transcriptomic inertness; variant impact is shaped by cellular context rather than sequence alone, establishing the variant-cell pair as a critical unit for interpreting somatic variation.

genetics↗

Genetic and Epigenetic Landscape of Self-Identified Hispanics/Latino in All Of Us

Human genetic studies still underrepresent many populations, limiting discovery and interpretation of medically relevant variation. Extensive admixture in self-identified Hispanic/Latino populations increases the need for representative reference data and ancestry-aware interpretation of medically relevant variation. We used long-read sequencing to analyze genetic variation, ancestry, and DNA methylation in 1,490 self-identified Hispanic/Latino participants from the All of Us Research Program. We identified 10 million novel variants and more than 100 candidate phenotype associations, with fine-mapping prioritizing structural variants over nearby single-nucleotide variants in more than half. We linked 3,329 tandem repeats to DNA methylation, resolved widespread allele-specific methylation, and identified ancestry-linked regulation across paralogous genes. These results reveal previously inaccessible genetic and regulatory variation and show the value of long-read sequencing for diverse populations.

genetics↗