Genome‐wide association study of body weight and conformation traits in neonatal sheep

2020 ◽  
Vol 51 (2) ◽  
pp. 336-340
Author(s):  
L. Tao ◽  
X. Y. He ◽  
L. X. Pan ◽  
J. W. Wang ◽  
S. Q. Gan ◽  
...  
PLoS ONE ◽  
2011 ◽  
Vol 6 (7) ◽  
pp. e21872 ◽  
Author(s):  
Xiaorong Gu ◽  
Chungang Feng ◽  
Li Ma ◽  
Chi Song ◽  
Yanqiang Wang ◽  
...  

Genomics ◽  
2019 ◽  
Vol 111 (6) ◽  
pp. 1583-1589 ◽  
Author(s):  
Qiang Yang ◽  
Pingxian Wu ◽  
Kai Wang ◽  
Dejuan Chen ◽  
Jie Zhou ◽  
...  

Genes ◽  
2021 ◽  
Vol 12 (8) ◽  
pp. 1170
Author(s):  
Jihye Cha ◽  
Hyojun Choo ◽  
Krishnamoorthy Srikanth ◽  
Seung-Hwan Lee ◽  
Ju-Whan Son ◽  
...  

Meat from Korean native chickens (KNCs) has high consumer demand; however, slow growth performance and high variation in body weight (BW) of KNCs remain an issue. Genome-wide association study (GWAS) is a powerful method to identify quantitative trait-associated genomic loci. A GWAS, based on a large-scale KNC population, is needed to identify underlying genetic mechanisms related to its growth traits. To identify BW-associated genomic regions, we performed a GWAS using the chicken 60K single nucleotide polymorphism (SNP) panel for 1328 KNCs. BW was measured at 8 weeks of age, from 2018 to 2020. Twelve SNPs were associated with BW at the suggestive significance level (p < 2.95 × 10−5) and located near or within 11 candidate genes, including WDR37, KCNIP4, SLIT2, PPARGC1A, MYOCD and ADGRA3. Gene set enrichment analysis based on the GWAS results at p < 0.05 (1680 SNPs) showed that 32 Gene Ontology terms and two Kyoto Encyclopedia of Genes and Genomes pathways, including regulation of transcription, motor activity, the mitogen-activated protein kinase signaling pathway, and tight junction, were significantly enriched (p < 0.05) for BW-associated genes. These pathways are involved in cell growth and development, related to BW gain. The identified SNPs are potential biomarkers in KNC breeding.


2018 ◽  
Vol 59 (3) ◽  
pp. 305-312 ◽  
Author(s):  
Fuwei Li ◽  
Haixia Han ◽  
Qiuxia Lei ◽  
Jinbo Gao ◽  
Jie Liu ◽  
...  

2019 ◽  
Vol 50 (3) ◽  
pp. 250-253 ◽  
Author(s):  
A. V. Igoshin ◽  
N. S. Yudin ◽  
N. M. Belonogova ◽  
D. M. Larkin

2017 ◽  
Author(s):  
Sandra Sanchez-Roige ◽  
Pierre Fontanillas ◽  
Sarah L. Elson ◽  
Anita Pandit ◽  
Ellen M. Schmidt ◽  
...  

ABSTRACTDelay discounting (DD), which is the tendency to discount the value of delayed versus current rewards, is elevated in a constellation of diseases and behavioral conditions. We performed a genome-wide association study of DD using 23,127 research participants of European ancestry. The most significantly associated SNP was rs6528024 (P = 2.40 × 10−8), which is located in an intron of the gene GPM6B. We also showed that 12% of the variance in DD was accounted for by genotype, and that the genetic signature of DD overlapped with attention-deficit/hyperactivity disorder, schizophrenia, major depression, smoking, personality, cognition, and body weight.


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