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ARS Home » Plains Area » Clay Center, Nebraska » U.S. Meat Animal Research Center » Livestock Bio-Systems » Research » Publications at this Location » Publication #229015

Title: MicroRNA expression profile in bovine cumulus-oocyte complexes during late oogenesis

item Miles, Jeremy
item McDaneld, Tara
item Wiedmann, Ralph
item Cushman, Robert - Bob
item Echternkamp, Sherrill
item Vallet, Jeff
item Smith, Timothy - Tim

Submitted to: Reproduction, Fertility and Development
Publication Type: Abstract Only
Publication Acceptance Date: 9/23/2008
Publication Date: 1/1/2009
Citation: Miles, J.R., McDaneld, T.G., Wiedmann, R.T., Cushman, R.A., Echternkamp, S.E., Vallet, J.L., Smith, T.P.L. 2009. MicroRNA expression profile in bovine cumulus-oocyte complexes during late oogenesis [abstract]. Reproduction, Fertility and Development. 21(1):186 (Abstract #174).

Interpretive Summary:

Technical Abstract: During late oogenesis, the mammalian oocyte synthesizes and stores mRNA necessary to guide the early stages of embryo development prior to the activation of embryonic transcription. The oocyte also contains many post-transcriptional regulatory mechanisms that coordinate mRNA stability and translation prior to specific activation. MicroRNAs (miRNAs) are short non-coding RNAs (17-25 nucleotides) that repress translation of target genes through sequence complementation and have recently been identified in murine oocytes. The objective of the current study was to identify and characterize the expression of miRNAs in bovine cumulus-oocyte complexes (COCs) during late oogenesis as a potential mechanism for post-transcriptional regulation of mRNA in developing bovine oocytes. Ovaries from beef cattle (mixed populations) were obtained at a local abattoir. COCs were aspirated from 2- to 10-mm follicles and COCs were pooled from each of five replicate collections for RNA extraction (n = 2241 total COCs). Small RNA in the 16 to 27 bp range was isolated and used to construct cDNA libraries for sequencing, producing 2529 successful sequences that were clustered based on matching 14 consecutive bases to the most common member of the cluster. The consensus sequences of the clusters were screened for mitochondrial RNA, rRNA, tRNA, and snoRNA contaminants, leading to removal of 774 (31%) sequences from consideration. The remaining 1755 putative miRNA sequences were compared to known miRNA in miRBase, revealing 62 bovine COC miRNA clusters matching previously known sequences and 4 with no match. The cluster with the largest number of sequences identified in bovine COCs matched the sequence of the let-7 miRNA family (657 sequences or 37% of putative miRNA). Within the let-7 family, let-7b (459 sequences or 26%) was the most abundant followed by let-7i (135 sequences or 8%). The four clusters that did not match sequences in miRBase represent putative novel miRNA. One of these four clusters had relatively high expression in bovine COCs (308 sequences or 18%) while the other three clusters had relatively low expression (total of 55 combined sequences or 3%). Expression of several putative miRNA (let-7b, let-7i, and miR-106a) in bovine COCs were confirmed using TaqMan miRNA assays. These results demonstrate the presence of miRNAs within bovine COCs during late oogenesis, which suggests that these post-transcriptional regulatory elements may play a role in coordinating mRNA stability and translation in bovine oocytes.