MicroRNA (miRNA) are small non-coding RNA, approximately 22 nucleotides in length, that regulate gene expression through their ability to bind to mRNA. The role of miRNA in cellular and tissue development is well documented and their importance in male reproductive tissue development is actively being evaluated. They are present in spermatogonia, Sertoli and Leydig cells within the testis and are present in mature spermatozoa, indicating roles in normal testicular development, function and spermatogenesis. Their presence in spermatozoa has led to postulations about the roles of male miRNA during early embryonic development after fertilisation, including chromatin restructuring and possible epigenetic effects on embryo development. MiRNAs are also present in body fluids, such as blood serum, milk, ovarian follicular fluid and seminal fluid. Circulating miRNAs are stable, and aberrant expression of cellular or extracellular miRNA has been associated with multiple pathophysiological conditions, the most studied being numerous forms of cancer. Considering that miRNAs are present in spermatozoa and in seminal fluid, their stability and the relatively non-invasive procedures required to obtain these samples make miRNAs excellent candidates for use as biomarkers of male reproduction and fertility. Biomarkers, such as miRNAs, identifying fertile males would be of financial interest to the animal production industry.
From 1981 through 1986, BW, hip height, and scrotal circumference (SC) measurements were obtained on 329 bulls at the start of a 140-d gain test (SOT) and every 28 d to the end of test (EOT). Age, overall ADG, weight per day of age, ADG by period, and SC growth (cm/d) were calculated. Data were analyzed in two data sets because age of dam (AOD) and birth weights were unavailable between 1981 and 1983. Correlations of SC to other traits measured and probabilities for bulls attaining 30 or 32 cm SC by 365 d of age were calculated. Two adjusted 365-d SC (365-d SC) were calculated for each individual from regression analysis and from the following formula: 365-d SC = [(SCEOT_ SCSOT)/140 d] × [365-ageSOT] + SCSOT. Except for ADG in Data Set 2, breed group differences (P < .05) were observed for correlations of SC to all growth traits, age, and AOD. To attain 30 cm SC by 365 d of age with nearly 100% probability, Angus, Simmental and Zebu-derived bulls needed a 23-cm SCSOT, whereas continental (other than Simmental) and Polled Hereford bulls required a 26-cm SCSOT. Overall, 365-d SC means calculated by regression analysis or formula method did not differ (P > .10) for either data set.