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      Pleomorphic adenoma gene1 in reproduction and implication for embryonic survival in cattle: a review

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          Abstract

          The pleomorphic adenoma gene1 ( PLAG1) encodes a DNA-binding, C 2H 2 zinc-finger protein which acts as a transcription factor that regulates the expression of diverse genes across different organs and tissues; hence, the name pleomorphic. Rearrangements of the PLAG1 gene, and/or overexpression, are associated with benign tumors and cancers in a variety of tissues. This is best described for pleomorphic adenoma of the salivary glands in humans. The most notable expression of PLAG1 occurs during embryonic and fetal development, with lesser expression after birth. Evidence has accumulated of a role for PLAG1 protein in normal early embryonic development and placentation in mammals. PLAG1 protein influences the expression of the ike growth factor 2 (IGF2) gene and production of IGF2 protein. IGF2 is an important mitogen in ovarian follicles/oocytes, embryos, and fetuses. The PLAG1-IGF2 axis, therefore, provides one pathway whereby PLAG1 protein can influence embryonic survival and pregnancy. PLAG1 also influences over 1,000 other genes in embryos including those associated with ribosomal assembly and proteins. Brahman ( Bos indicus) heifers homozygous for the PLAG1 variant, rs109815800 (G > T), show greater fertility than contemporary heifers with either one, or no copy, of the variant. Greater fertility in heifers homozygous for rs109815800 could be the result of early puberty and/or greater embryonic survival. The present review first looks at the broader roles of the PLAG1 gene and PLAG1 protein and then focuses on the emerging role of PLAG1/PLAG1 in embryonic development and pregnancy. A deeper understanding of factors which influence embryonic development is required for the next transformational increase in embryonic survival and successful pregnancy for both in vivo and in vitro derived embryos in cattle.

          Abstract

          This review explores how the pleomorphic adenoma gene1 ( PLAG1) which is associated with cancers may also be fundamentally important in embryonic development and the establishment of pregnancy in mammals.

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          Most cited references156

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          The many faces and functions of β-catenin.

          β-Catenin (Armadillo in Drosophila) is a multitasking and evolutionary conserved molecule that in metazoans exerts a crucial role in a multitude of developmental and homeostatic processes. More specifically, β-catenin is an integral structural component of cadherin-based adherens junctions, and the key nuclear effector of canonical Wnt signalling in the nucleus. Imbalance in the structural and signalling properties of β-catenin often results in disease and deregulated growth connected to cancer and metastasis. Intense research into the life of β-catenin has revealed a complex picture. Here, we try to capture the state of the art: we try to summarize and make some sense of the processes that regulate β-catenin, as well as the plethora of β-catenin binding partners. One focus will be the interaction of β-catenin with different transcription factors and the potential implications of these interactions for direct cross-talk between β-catenin and non-Wnt signalling pathways.
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            Genomic imprinting in mammals.

            Genomic imprinting affects a subset of genes in mammals and results in a monoallelic, parental-specific expression pattern. Most of these genes are located in clusters that are regulated through the use of insulators or long noncoding RNAs (lncRNAs). To distinguish the parental alleles, imprinted genes are epigenetically marked in gametes at imprinting control elements through the use of DNA methylation at the very least. Imprinted gene expression is subsequently conferred through lncRNAs, histone modifications, insulators, and higher-order chromatin structure. Such imprints are maintained after fertilization through these mechanisms despite extensive reprogramming of the mammalian genome. Genomic imprinting is an excellent model for understanding mammalian epigenetic regulation.
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              Parental imprinting of the mouse insulin-like growth factor II gene.

              We are studying mice that carry a targeted disruption of the gene encoding insulin-like growth factor II (IGF-II). Transmission of this mutation through the male germline results in heterozygous progeny that are growth deficient. In contrast, when the disrupted gene is transmitted maternally, the heterozygous offspring are phenotypically normal. Therefore, the difference in growth phenotypes depends on the type of gamete contributing the mutated allele. Homozygous mutants are indistinguishable in appearance from growth-deficient heterozygous siblings. Nuclease protection and in situ hybridization analyses of the transcripts from the wild-type and mutated alleles indicate that only the paternal allele is expressed in embryos, while the maternal allele is silent. An exception is the choroid plexus and leptomeninges, where both alleles are transcriptionally active. These results demonstrate that IGF-II is indispensable for normal embryonic growth and that the IGF-II gene is subject to tissue-specific parental imprinting.
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                Author and article information

                Contributors
                Journal
                J Anim Sci
                J Anim Sci
                jansci
                Journal of Animal Science
                Oxford University Press (US )
                0021-8812
                1525-3163
                2024
                08 April 2024
                08 April 2024
                : 102
                : skae103
                Affiliations
                School of Life and Environmental Sciences, Faculty of Science, The University of Sydney , Sydney, NSW, Australia
                Department of Veterinary Medicine and Animal Production, University of Naples Federico II , Naples, Italy
                Faculty of Veterinary Medicine and Animal Science, Department of Animal Reproduction, University of Sao Paulo , Sao Paulo, Brazil
                CSIRO, Agriculture and Food , Brisbane, QLD, Australia
                Queensland Alliance for Agriculture and Food Innovation, The University of Queensland , Brisbane, QLD, Australia
                CBV Brahman, Marlborough, Central Queensland , QLD, Australia
                School of Chemistry and Molecular Biosciences, The University of Queensland , Brisbane, QLD, Australia
                Author notes
                Author information
                https://orcid.org/0000-0002-7254-1960
                Article
                skae103
                10.1093/jas/skae103
                11056886
                38586898
                cde04380-9067-43af-89fd-1da71a40b32f
                © The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 07 December 2023
                : 05 April 2024
                : 29 April 2024
                Page count
                Pages: 12
                Categories
                Reproduction
                AcademicSubjects/SCI00960

                cattle,embryo,pleomorphic adenoma gene,plag1
                cattle, embryo, pleomorphic adenoma gene, plag1

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