A novel approach to sexing bovine blastocysts using male-specific gene expression

• Published in: Theriogenology Vol. 77; no. 8; pp. 1587 - 1596
• Main Authors: Hamilton, C.K, Combe, A, Caudle, J, Ashkar, F.A, Macaulay, A.D, Blondin, P, King, W.A
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.05.2012
• Subjects: Animals; Blastocyst - metabolism; Bovine embryo; cattle; Cattle - genetics; Development; Female; Fertilization in Vitro - veterinary; gene expression; genes; Genes, Y-Linked; Male; reverse transcriptase polymerase chain reaction; Reverse Transcription; RNA, Messenger - metabolism; RNA-directed DNA polymerase; Sex determination; Sex Determination Analysis - methods; Sex Determination Analysis - veterinary; Sex Factors; sexing; Sexual dimorphism; Y chromosome; Development; Bovine embryo; Sexual dimorphism; Sex determination; Y chromosome
• ISSN: 0093-691X; 1879-3231
• DOI: 10.1016/j.theriogenology.2011.11.027

When examining gene expression profiles for the purposes of assessing embryo quality, it is imperative that sex be considered, because many embryonic transcripts have sex-related expression patterns. The objective of this study was to systematically examine eight Y chromosome linked genes (DDX3Y, EIF1AY, HSFY, SRY, TSPY, USP9Y, ZFY, and ZRSR2Y) to characterize their expression in bovine blastocysts and to examine the usefulness of this expression for the purpose of RNA-based embryo sexing. In order to examine the expression of these genes, pools of blastocysts (groups of 10 and 20) as well as single embryos (N = 50) were analyzed with reverse transcriptase polymerase chain reaction (RT-PCR) and reverse transcriptase quantitative PCR (RT-qPCR). Of the 50 single embryos, 32 were concurrently sexed with DNA-based methods. Transcripts of DDX3Y, EIF1AY, TSPY, USP9Y, ZFY and ZRSR2Y were detected in the pooled and single blastocysts, but no transcripts were detected for HSFY or SRY. After performing DNA-based sexing experiments, we concluded that this expression was restricted to the male embryos. The consistency of the expression varied according to the gene as well as the specific primer set. Three genes were expressed in the full set of male embryos, DDX3Y, USP9Y, and ZRSR2Y and therefore represent good candidates for RNA-based sexing methods.