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      Development of a formula for scoring competence of bovine embryos to sustain pregnancy

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      a , * , b
      Biochemistry and Biophysics Reports
      Elsevier

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          Abstract

          Embryo transfer in cattle and other species is a key reproductive technology to improve genetic merit. However, pregnancy loss after embryo transfer is still a major barrier to optimal utilization of the technology. Furthermore, the lack of a method to objectively quantify embryonic competence hinders investigations aimed at improving the competence of an embryo. Based on the knowledge that bovine embryos have an inherent molecular signature that determines their ability for pregnancy establishment which can result in distinct gene expression profiles, we have previously integrated transcriptomic data from independent experiments to identify eight genes capable of predicting embryo competence for survival with high accuracy. In this study, we developed a function for the R software containing a mathematical formula based on the model coefficients to yield an embryonic competence index (ECI) according to the expression of those eight critical genes. Application of the function to a gene expression dataset generates a quantitative ECI value for each embryo that can be employed in statistical analyses when performing an experiment. The folder with the R project and required datasets can be found in https://zenodo.org/records/12515587.

          Highlights

          • In cattle, pregnancy loss after embryo transfer diminishes reproductive efficiency.

          • There is no method to objectively quantify the embryo ability to sustain pregnancy.

          • Previously, we identified eight biomarker genes that predicted embryo competence.

          • Based on these genes, we developed a formula to calculate embryo competence index.

          • Here, we introduce an R function that yields the index in an expression dataset.

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          Most cited references21

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          Uterine influences on conceptus development in fertility-classified animals

          Successful pregnancy establishment requires synchronous interactions of the conceptus with the endometrium of the uterus. This study of pregnancy outcome after assisted reproduction in fertility-classified cattle determined how the uterine environment impacts and programs conceptus survival and development. The study found that ripple effects of dysregulated conceptus–endometrial interactions elicit postelongation pregnancy loss in subfertile animals during the implantation period. This research enhances our understanding of the mechanisms that lead to pregnancy loss in both natural and assisted reproduction and has wide implications for improving pregnancy success in domestic animals and humans. A major unresolved issue is how the uterus influences infertility and subfertility in cattle. Serial embryo transfer was previously used to classify heifers as high-fertile (HF), subfertile (SF), or infertile (IF). To assess pregnancy loss, two in vivo-produced embryos were transferred into HF, SF, and IF heifers on day 7, and pregnancy outcome was assessed on day 17. Pregnancy rate was substantially higher in HF (71%) and SF (90%) than IF (20%) heifers. Elongating conceptuses were about twofold longer in HF than SF heifers. Transcriptional profiling detected relatively few differences in the endometrium of nonpregnant HF, SF, and IF heifers. In contrast, there was a substantial difference in the transcriptome response of the endometrium to pregnancy between HF and SF heifers. Considerable deficiencies in pregnancy-dependent biological pathways associated with extracellular matrix structure and organization as well as cell adhesion were found in the endometrium of SF animals. Distinct gene expression differences were also observed in conceptuses from HF and SF animals, with many of the genes decreased in SF conceptuses known to be embryonic lethal in mice due to defects in embryo and/or placental development. Analyses of biological pathways, key players, and ligand–receptor interactions based on transcriptome data divulged substantial evidence for dysregulation of conceptus–endometrial interactions in SF animals. These results support the ideas that the uterus impacts conceptus survival and programs conceptus development, and ripple effects of dysregulated conceptus–endometrial interactions elicit loss of the postelongation conceptus in SF cattle during the implantation period of pregnancy.
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            Zygotic and embryonic gene expression in cow: a review of timing and mechanisms of early gene expression as compared with other species.

            Early embryonic development is largely dependent on maternal RNAs and proteins synthesised during oogenesis. Zygotic transcription is an essential event that occurs at a species-specific time after fertilization. In the absence of zygotic transcription the embryo dies since it can no longer support requirements for successful embryo development. Molecular genetics of gene expression during early embryogenesis, especially in the bovine species, remain one of the unsolved questions in modern biology. Earlier studies suggested that embryonic transcription in cattle begins at the late 4-cell or 8-cell stage. However, more recent studies suggest that bovine zygotes and 2-cell embryos are both transcriptionally and translationally active. Moreover, changes in chromatin structure due to acetylation of core histones and DNA replication play important roles in the regulation of zygotic/embryonic gene expression. This review will summarise results of recent studies about the timing and mechanisms of zygotic/embryonic gene expression in cattle. In addition, terminology in the literature regarding gene expression during early embryogenesis will be clarified. These terminologies include: 'zygotic/embryonic gene expression', 'maternal to embryonic transition in control of development (MET)' and 'zygotic/embryonic genome activation (ZEGA)'.
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              Symposium review: How to implement genomic selection

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                Author and article information

                Contributors
                Journal
                Biochem Biophys Rep
                Biochem Biophys Rep
                Biochemistry and Biophysics Reports
                Elsevier
                2405-5808
                02 July 2024
                September 2024
                02 July 2024
                : 39
                : 101772
                Affiliations
                [a ]Department of Population Health Science, Faculty of Veterinary Medicine, Utrecht University, 3584 CL, Utrecht, the Netherlands
                [b ]Dept. of Animal Sciences, University of Florida, Gainesville, FL, USA
                Author notes
                [* ]Corresponding author. m.b.rabaglino@ 123456uu.nl
                Article
                S2405-5808(24)00136-5 101772
                10.1016/j.bbrep.2024.101772
                11268127
                39050012
                de42a539-0598-4463-a7c4-02b1a2d4fcea
                © 2024 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 18 April 2024
                : 24 June 2024
                : 28 June 2024
                Categories
                Short Communication

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