2014
DOI: 10.1016/j.anireprosci.2014.01.012
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Genome-wide association study for poor sperm motility in Holstein-Friesian bulls

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Cited by 87 publications
(67 citation statements)
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“…Genes underlying the volume of semen and total number of sperm in ejaculate of fertile bulls were not studied. In our earlier work (Hering et al, 2014) we found SNP markers associated with extremely poor sperm motility and suggest some candidate genes involved in this undesirable trait. The aim of this work is to identify markers and candidate genes associated with the variation in semen volume and total number of sperm -traits of high importance for AI stations.…”
Section: Introductionmentioning
confidence: 75%
“…Genes underlying the volume of semen and total number of sperm in ejaculate of fertile bulls were not studied. In our earlier work (Hering et al, 2014) we found SNP markers associated with extremely poor sperm motility and suggest some candidate genes involved in this undesirable trait. The aim of this work is to identify markers and candidate genes associated with the variation in semen volume and total number of sperm -traits of high importance for AI stations.…”
Section: Introductionmentioning
confidence: 75%
“…Based on the Genome-Wise Association Study in bulls we found that the genetic marker rs29011704 located at a distance of 807 214 bp from the SOX5 gene is significantly associated with sperm motility in bulls (Hering et al 2014). As previously noted (Kiselak et al 2010) S-SOX5 (48-kDa SOX5 protein) plays a key role in the formation and function of motile cilia.…”
Section: Introductionmentioning
confidence: 75%
“…ksk Within these 25 STRs, we indeed found seven genes which may involve in selection signature: FAM171B, INHBB, TFCP2L1, RPRD2, KLHL1, SP2, and WRN. Three of these loci are of particular interest: INHBB has an important role of inhibin in reproduction (Chu et al 2011;Lee et al 2013); KLHL1 is involved in poor sperm motility in Holstein-Friesian bulls (Shin et al 2014;Hering et al 2014); and WRN gene is related to Werner syndrome (WS), also known as "adult progeria", a rare and autosomal recessive progeroid syndrome (PS), which was characterized by the appearance of premature aging (Doan et al 2012).…”
Section: Selection and Population Genetic Analyses Of Microsatellitesmentioning
confidence: 99%