Genome-wide association study for age at puberty in young Nelore bulls.
Nedenia Bonvino StafuzzaEliane Vianna da Costa E SilvaRafael Medeiros de Oliveira SilvaLuiz Carlos Cesar da Costa FilhoFernanda Battistotti BarbosaGustavo Guerino MacedoRaysildo B LoboFernando BaldiPublished in: Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie (2019)
Selection for bulls that would reach puberty early reduces the generation interval and increases fertility and herd productivity. Despite its economic importance, there are few QTL associated with age at puberty described in the literature. In this study, a weighted single-step genome-wide association study was performed to detect genomic regions and putative candidate genes related to age at puberty in young Nelore bulls. Several protein-coding genes related to spermatogenesis functions were identified within the genomic regions that explain more than 0.5% of the additive genetic variance for age at puberty in Nelore bulls, such as ADAM11, BRCA1, CSNK2A, CREBBP, MEIOC, NDRG2, NECTIN3, PARP2, PARP9, PRSS21, RAD51C, RNASE4, SLX4, SPA17, TEX14, TIMP2 and TRIP13 gene. Enrichment analysis by DAVID also revealed several GO terms related to spermatogenesis such as DNA replication (GO:0006260), male meiosis I (GO:0007141), double-strand break repair (GO:0006302), base excision repair (GO:0006284), apoptotic process (GO:0006915), cell-cell adhesion (GO: 0098609) and focal adhesion (GO:0005925). The heritability for age at puberty shows that this trait can be improved based on traditional EBV selection. Adding genomic information to the system helps to elucidate genes and molecular mechanisms controlling the sexual precocity and could help to predict sexual precocity in Nelore bulls with greater accuracy at younger age, which would speed up the breeding programme for this breed.
Keyphrases
- genome wide association study
- genome wide
- copy number
- dna damage
- dna repair
- single cell
- cell adhesion
- systematic review
- gene expression
- clinical trial
- stem cells
- computed tomography
- magnetic resonance imaging
- escherichia coli
- mental health
- climate change
- oxidative stress
- randomized controlled trial
- young adults
- small molecule
- study protocol
- cell therapy
- health information
- protein protein
- pseudomonas aeruginosa
- breast cancer risk