Whole-genome resequencing of Ujumqin sheep to investigate the determinants of the multi-vertebral trait

Genome ◽  
2018 ◽  
Vol 61 (9) ◽  
pp. 653-661 ◽  
Author(s):  
Shuo Li ◽  
Rongsong Luo ◽  
Defang Lai ◽  
Min Ma ◽  
Fei Hao ◽  
...  
Keyword(s):  
Nucleotide Polymorphisms ◽  
Genome Resequencing ◽  
Single Nucleotide ◽  
Frameshift Mutations ◽  
Synonymous Mutations ◽  
Coding Regions ◽  
Homozygous Mutations ◽  
Vertebral Development ◽  
Whole Genome Resequencing ◽  
Genomic Regions

The Ujumqin sheep is one of the most profitable breeds in China, with unique multi-vertebral characteristics. We performed high-throughput genome resequencing of five multi-vertebral and three non-multi-vertebral sheep in an Ujumqin population. We identified the genomic regions that correlated with the germplasm characteristics to establish the cause of the “multi-vertebral” phenotype in this breed. Sequencing generated a total of 314 952 000 000 bp of raw data. The alignment rate of all the samples was between 98.53% and 99.11%, and the mean depth of coverage relative to the reference genome was between 11.58× and 14.92×. After comparing the differences between the two groups, we identified 21 homozygous single nucleotide polymorphisms (SNPs) in the mutant exons of 14 genes. Nineteen loci of 10 genes contained nonsynonymous mutations, while two loci contained synonymous mutations. Resequencing revealed homozygous mutations comprised of 44 indels located within exons of 19 genes. These indels included 37 frameshift mutations, 6 non-frameshift mutations, and 1 stopgain single nucleotide variation (SNV). Finally, comparisons of genotypic variations revealed 17 genes with homozygous mutations in their coding regions, 5 of which have previously been associated with vertebral development and the remaining 12 genes were newly identified in this study.

scholarly journals The evolutionary history and genomics of European blackcap migration

eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Kira Delmore ◽  
Juan Carlos Illera ◽  
Javier Pérez-Tris ◽  
Gernot Segelbacher ◽  
Juan S Lugo Ramos ◽  
...  
Keyword(s):  
Seasonal Migration ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide ◽  
Rapid Changes ◽  
Migratory Syndrome ◽  
Enormous Variation ◽  
Whole Genome Resequencing ◽  
Genomic Regions ◽  
Admixture Event ◽  
Shared Variation

Seasonal migration is a taxonomically widespread behaviour that integrates across many traits. The European blackcap exhibits enormous variation in migration and is renowned for research on its evolution and genetic basis. We assembled a reference genome for blackcaps and obtained whole genome resequencing data from individuals across its breeding range. Analyses of population structure and demography suggested divergence began ~30,000 ya, with evidence for one admixture event between migrant and resident continent birds ~5000 ya. The propensity to migrate, orientation and distance of migration all map to a small number of genomic regions that do not overlap with results from other species, suggesting that there are multiple ways to generate variation in migration. Strongly associated single nucleotide polymorphisms (SNPs) were located in regulatory regions of candidate genes that may serve as major regulators of the migratory syndrome. Evidence for selection on shared variation was documented, providing a mechanism by which rapid changes may evolve.

scholarly journals Development a Set of 46 SNP Markers for the Yellow Catfish (Tachysurus Fulvidraco)

2021 ◽  
Author(s):  
Huaxing Zhou ◽  
Tingshuang Pan ◽  
Huan Wang ◽  
He Jiang ◽  
Jun Ling ◽  
...  
Keyword(s):  
Snp Markers ◽  
Whole Genome ◽  
Nucleotide Polymorphisms ◽  
Yellow Catfish ◽  
Genome Resequencing ◽  
Single Nucleotide ◽  
Expected Heterozygosity ◽  
Hardy Weinberg Equilibrium ◽  
Whole Genome Resequencing ◽  
Tachysurus Fulvidraco

Abstract The whole genome resequencing was used to develop single nucleotide polymorphisms (SNP) markers for the yellow catfish (Tachysurus fulvidraco). A total of 46 SNP markers were selected from 5550676 genotyping markers which distributed on 26 chromosomes. Of the 46 SNPs analyzed, 35 SNPs conformed to Hardy-Weinberg equilibrium. The observed and expected heterozygosity of these markers ranged from 0.2519 to 0.771 and from 0.265 to 0.5018, respectively. This set of markers will be of great useful for population genetics of the yellow catfish.

scholarly journals Whole Genome Resequencing of Arkansas Progressor and Regressor Line Chickens to Identify SNPs Associated with Tumor Regression

Genes ◽  
2018 ◽  
Vol 9 (10) ◽  
pp. 512
Author(s):  
Bhuwan Khatri ◽  
Ashley M. Hayden ◽  
Nicholas B. Anthony ◽  
Byungwhi C. Kong
Keyword(s):  
Network Analysis ◽  
Genetic Factors ◽  
Tumor Regression ◽  
Read Depth ◽  
Whole Genome ◽  
Nucleotide Polymorphisms ◽  
Genome Resequencing ◽  
Synonymous Mutations ◽  
Regression Property ◽  
Whole Genome Resequencing

Arkansas Regressor (AR) chickens, unlike Arkansas Progressor (AP) chickens, regress tumors induced by the v-src oncogene. To better understand the genetic factors responsible for this tumor regression property, whole genome resequencing was conducted using Illumina Hi-Seq 2 × 100 bp paired-end read method (San Diego, CA, USA) with AR (confirmed tumor regression property) and AP chickens. Sequence reads were aligned to the chicken reference genome (galgal5) and produced coverage of 11× and 14× in AR and AP, respectively. A total of 7.1 and 7.3 million single nucleotide polymorphisms (SNPs) were present in AR and AP genomes, respectively. Through a series of filtration processes, a total of 12,242 SNPs were identified in AR chickens that were associated with non-synonymous, frameshift, nonsense, no-start and no-stop mutations. Further filtering of SNPs based on read depth ≥ 10, SNP% ≥ 0.75, and non-synonymous mutations identified 63 reliable marker SNPs which were chosen for gene network analysis. The network analysis revealed that the candidate genes identified in AR chickens play roles in networks centered to ubiquitin C (UBC), phosphoinositide 3-kinases (PI3K), and nuclear factor kappa B (NF-kB) complexes suggesting that the tumor regression property in AR chickens might be associated with ubiquitylation, PI3K, and NF-kB signaling pathways. This study provides an insight into genetic factors that could be responsible for the tumor regression property.

scholarly journals Genetic Mutation Analysis of High and Low IgY Chickens by Capture Sequencing

Animals ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 272 ◽  
Author(s):  
Qiao Wang ◽  
Fei Wang ◽  
Lu Liu ◽  
Qinghe Li ◽  
Ranran Liu ◽  
...  
Keyword(s):  
Genome Wide Association Study ◽  
Genetic Mutation ◽  
Genetic Mutations ◽  
Nucleotide Polymorphisms ◽  
White Leghorn ◽  
Single Nucleotide ◽  
Synonymous Mutations ◽  
Genome Wide ◽  
Genomic Regions ◽  
Capture Sequencing

Based on the results of our previous genome-wide association study (GWAS), a comprehensive analysis on single nucleotide polymorphisms (SNPs) was performed on White Leghorn and Beijing-You chickens with high and low IgY levels in defined genomic regions using the capture-sequencing approach. High and low IgY chickens showed substantial genetic variations. In total, more than 30,000 SNPs were found in all four chicken groups, among which 1045 were non-synonymous mutations resulting in amino acids alterations. In total, 23,309 Indels were identified. Among the 1169 Indels that were found only in Beijing-You chickens, 702 were shared between high and low IgY chickens compared with the reference genome. There were 1016 Indels specific to the White Leghorn chickens, among which 188 were high IgY-specific, 134 were low IgY-specific and 694 were shared between the high and low IgY chicken lines. Many genetic mutations were located in the regulatory regions of important immunomodulatory genes, including TAP1, TAP2 and BF1. Our findings provide an in-depth understanding of genetic mutations in chicken microchromosomes.

scholarly journals Genome-wide variations analysis of special waxy sorghum cultivar Hongyingzi for brewing Moutai liquor

2019 ◽  
Author(s):  
Can Wang ◽  
Lingbo Zhou ◽  
Xu Gao ◽  
Yanqing Ding ◽  
Bin Cheng ◽  
...  
Keyword(s):  
Chalcone Synthase ◽  
Reference Genome ◽  
Copy Number Variations ◽  
Whole Genome ◽  
Nucleotide Polymorphisms ◽  
Structural Variations ◽  
Genome Resequencing ◽  
Single Nucleotide ◽  
Genome Wide ◽  
Whole Genome Resequencing

AbstractsHongyingzi is a special waxy sorghum (Sorghum bicolor L. Moench) cultivar for brewing Moutai liquor. For an overall understanding of the whole genome of Hongyingzi, we performed whole-genome resequencing technology with 56.10 X depth to reveal its comprehensive variations. Compared with the BTx623 reference genome, 2.48% of genome sequences were altered in the Hongyingzi genome. Among these alterations, there were 1885774 single nucleotide polymorphisms (SNPs), 309381 small fragments insertions and deletions (Indels), 31966 structural variations (SVs), and 217273 copy number variations (CNVs). These alterations conferred 29614 genes variations. It was also predicted that 35 genes variations were related to the multidrug and toxic efflux (MATE) transporter, chalcone synthase (CHS), ATPase isoform 10 (AHA10) transporter, dihydroflavonol-4-reductase (DFR), the laccase 15 (LAC15), flavonol 3′-hydroxylase (F3′H), flavanone 3-hydroxylase (F3H), O-methyltransferase (OMT), flavonoid 3′5′ hydroxylase (F3′5′H), UDP-glucose:sterol-glucosyltransferase (SGT), flavonol synthase (FLS), and chalcone isomerase (CHI) involved in the tannin synthesis. These results would provide theoretical supports for the molecular markers developments and gene function studies related to the liquor-making traits, and the genetic improvement of waxy sorghum based on the genome editing technology.

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