부산대학교 도서관

To purchase or authenticate to the full-text of this article, please visit this link: http://dx.doi.org/10.1111/j.1439-0531.2006.00708.x Byline: S Mamo (1), CA Sargent (2), NA Affara (2), D Tesfaye (1), N El-Halawany (1), K Wimmers (1), M Gilles (1), K Schellander (1), S Ponsuksili (1) Abstract: Contents To study the mRNA transcript profiles of some potential candidate developmental genes during bovine oocyte and blastocyst stages, RNA amplification procedures, cDNA microarray of 82 target genes spotted onto glass slide and real-time polymerase chain reaction (PCR) were used. Messenger RNAs were isolated from in vitro-produced bovine matured oocytes and blastocysts. Using equal amounts of input mRNAs but different cycles of amplifications, cDNAs were produced and served as template for RNA amplification by the in vitro transcriptions. After amplification, the RNA yields transcribed from cDNAs of different cycles were evaluated both by hybridization on the cDNA microarrays and by using real-time PCR techniques. The analyses indicated best results from lower amplification cycle templates with consistent signals at hybridization. Generally, the RNA yield was directly proportional to the amplification cycle but inversely related with signal consistency at repeated hybridizations. Using the protocols established, equal amounts of amplified RNA from matured oocytes and blastocysts were hybridized to the array. Analyses of replicated hybridizations indicated that 35 transcripts were differentially expressed. Most of these were not described in previous bovine embryo studies. Independent analyses of 23 transcripts with real-time PCR and unamplified RNA confirmed the results of 22 genes. Moreover, the functional analyses showed various roles related to development. Hence, it is possible to conclude that the genes identified here are potential candidates for characterizing developmental competence, and that the methods established can be used for large-scale gene expression analysis with more comprehensive arrays. Author Affiliation: (1)Institute of Animal Breeding Sciences, University of Bonn, Bonn, Germany (2)Department of Pathology, Tennis Court Road, Cambridge, UK Article History: Submitted: 09.01.2006 Article note: Author's address (for correspondence): S Ponsuksili, Research Institute for the Biology of Farm Animals, Dummerstorf, Germany. E-mail: toyotas7@excite.com, Current address: S Mamo, Department of Animal Biology, Agricultural Biotechnology centre, Godollő, Hungary, Current address: K Wimmers, Research Institute for the Biology of Farm Animals, Dummerstorf, Germany