Hering D M, Oleński K, Ruść A, Kaminski S
University of Warmia and Mazury in Olsztyn, Department of Animal Genetics, 10-719 Olsztyn, Poland.
University of Warmia and Mazury in Olsztyn, Department of Animal Genetics, 10-719 Olsztyn, Poland.
Anim Reprod Sci. 2014 Dec 30;151(3-4):126-30. doi: 10.1016/j.anireprosci.2014.10.022. Epub 2014 Nov 1.
In artificial insemination industry bulls producing high volume of semen with relatively high concentration of sperm are very desirable since they ensure stable production of commercial straws especially in case of top bulls. The aim of the study was to screen the entire bull genome to identify markers and candidate genes underlying semen volume (SV) and total number of sperm (TNS) in ejaculate produced by Holstein-Friesian bulls. Data on semen production were retrieved from records of AI center and included a population of 877 Holstein-Friesian bulls. Each bull was genotyped using the Illumina BovineSNP50 BeadChip. Genome-wide association analysis was performed with the use of GoldenHelix SVS7 software. An additive model for Linear Regression Analysis was used to estimate the effect of SNP marker for SV and TNS. After Bonferroni correction, 3 markers located on chromosome 22 reached the highest significance (rs41625599, rs41584616, rs42012507) for both traits. In the vicinity of these significant markers 3 genes are located (DCP1A, SFMBT1, TMEM110). Moreover, marker rs110109069 located on chromosome 25 was significantly associated with TNS and marker rs42438348 located on chromosome 10 has been found to be associated with SV. Some additional candidate genes were suggested to be potentially involved in analyzed traits (GALC, PRKCD, PHF7, TLR9, SPATA7). Identifying SNPs associated with the lower total number of sperm may be very useful for early recognition of a young sire as less suitable for effective semen production in artificial insemination centers.
在人工授精行业,能产生大量精液且精子浓度相对较高的种公牛非常受欢迎,因为它们能确保稳定生产商业细管精液,尤其是对于顶级种公牛而言。本研究的目的是筛选整个公牛基因组,以确定荷斯坦 - 弗里生公牛射精量(SV)和精子总数(TNS)背后的标记和候选基因。精液生产数据从人工授精中心的记录中获取,包括877头荷斯坦 - 弗里生公牛。每头公牛使用Illumina BovineSNP50 BeadChip进行基因分型。使用GoldenHelix SVS7软件进行全基因组关联分析。线性回归分析的加性模型用于估计SNP标记对SV和TNS的影响。经过Bonferroni校正后,位于22号染色体上的3个标记(rs41625599、rs41584616、rs42012507)对这两个性状均达到最高显著性。在这些显著标记附近定位到3个基因(DCP1A、SFMBT1、TMEM110)。此外,位于25号染色体上的标记rs110109069与TNS显著相关,位于10号染色体上的标记rs42438348与SV相关。还提出了一些额外的候选基因可能潜在参与所分析的性状(GALC、PRKCD、PHF7、TLR9、SPATA7)。识别与精子总数较低相关的单核苷酸多态性(SNP)对于早期识别不太适合在人工授精中心进行有效精液生产的年轻种公牛可能非常有用。