» Articles » PMID: 25653314

Combined QTL and Selective Sweep Mappings with Coding SNP Annotation and Cis-eQTL Analysis Revealed PARK2 and JAG2 As New Candidate Genes for Adiposity Regulation

Abstract

Very few causal genes have been identified by quantitative trait loci (QTL) mapping because of the large size of QTL, and most of them were identified thanks to functional links already known with the targeted phenotype. Here, we propose to combine selection signature detection, coding SNP annotation, and cis-expression QTL analyses to identify potential causal genes underlying QTL identified in divergent line designs. As a model, we chose experimental chicken lines divergently selected for only one trait, the abdominal fat weight, in which several QTL were previously mapped. Using new haplotype-based statistics exploiting the very high SNP density generated through whole-genome resequencing, we found 129 significant selective sweeps. Most of the QTL colocalized with at least one sweep, which markedly narrowed candidate region size. Some of those sweeps contained only one gene, therefore making them strong positional causal candidates with no presupposed function. We then focused on two of these QTL/sweeps. The absence of nonsynonymous SNPs in their coding regions strongly suggests the existence of causal mutations acting in cis on their expression, confirmed by cis-eQTL identification using either allele-specific expression or genetic mapping analyses. Additional expression analyses of those two genes in the chicken and mice contrasted for adiposity reinforces their link with this phenotype. This study shows for the first time the interest of combining selective sweeps mapping, coding SNP annotation and cis-eQTL analyses for identifying causative genes for a complex trait, in the context of divergent lines selected for this specific trait. Moreover, it highlights two genes, JAG2 and PARK2, as new potential negative and positive key regulators of adiposity in chicken and mice.

Citing Articles

Insights into trait-association of selection signatures and adaptive eQTL in indigenous African cattle.

Friedrich J, Liu S, Fang L, Prendergast J, Wiener P BMC Genomics. 2024; 25(1):981.

PMID: 39425030 PMC: 11490109. DOI: 10.1186/s12864-024-10852-8.


Sporadic occurrence of recent selective sweeps from standing variation in humans as revealed by an approximate Bayesian computation approach.

Laval G, Patin E, Boutillier P, Quintana-Murci L Genetics. 2021; 219(4).

PMID: 34849862 PMC: 8664576. DOI: 10.1093/genetics/iyab161.


RNA-Seq Data for Reliable SNP Detection and Genotype Calling: Interest for Coding Variant Characterization and -Regulation Analysis by Allele-Specific Expression in Livestock Species.

Jehl F, Degalez F, Bernard M, Lecerf F, Lagoutte L, Desert C Front Genet. 2021; 12:655707.

PMID: 34262593 PMC: 8273700. DOI: 10.3389/fgene.2021.655707.


Genome-wide detection of signatures of selection in indicine and Brazilian locally adapted taurine cattle breeds using whole-genome re-sequencing data.

Peripolli E, Reimer C, Ha N, Geibel J, Machado M, do Carmo Panetto J BMC Genomics. 2020; 21(1):624.

PMID: 32917133 PMC: 7488563. DOI: 10.1186/s12864-020-07035-6.


Discovery and Functional Annotation of Quantitative Trait Loci Affecting Resistance to Sea Lice in Atlantic Salmon.

Robledo D, Gutierrez A, Barria A, Lhorente J, Houston R, Yanez J Front Genet. 2019; 10:56.

PMID: 30800143 PMC: 6375901. DOI: 10.3389/fgene.2019.00056.


References
1.
Beaumont M, Balding D . Identifying adaptive genetic divergence among populations from genome scans. Mol Ecol. 2004; 13(4):969-80. DOI: 10.1111/j.1365-294x.2004.02125.x. View

2.
Li S, Qian J, Yang Y, Zhao W, Dai J, Bei J . GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers. PLoS Genet. 2012; 8(7):e1002791. PMC: 3395595. DOI: 10.1371/journal.pgen.1002791. View

3.
Lewontin R, KRAKAUER J . Distribution of gene frequency as a test of the theory of the selective neutrality of polymorphisms. Genetics. 1973; 74(1):175-95. PMC: 1212935. DOI: 10.1093/genetics/74.1.175. View

4.
Chirgwin J, Przybyla A, MacDonald R, Rutter W . Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry. 1979; 18(24):5294-9. DOI: 10.1021/bi00591a005. View

5.
Uhrig R, She Y, Leach C, Plaxton W . Regulatory monoubiquitination of phosphoenolpyruvate carboxylase in germinating castor oil seeds. J Biol Chem. 2008; 283(44):29650-7. PMC: 2662052. DOI: 10.1074/jbc.M806102200. View