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      Implications of the polymorphism of HLA-G on its function, regulation, evolution and disease association

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          Abstract

          The HLA- G gene displays several peculiarities that are distinct from those of classical HLA class I genes. The unique structure of the HLA-G molecule permits a restricted peptide presentation and allows the modulation of the cells of the immune system. Although polymorphic sites may potentially influence all biological functions of HLA-G, those present at the promoter and 3′ untranslated regions have been particularly studied in experimental and pathological conditions. The relatively low polymorphism observed in the MHC-G coding region both in humans and apes may represent a strong selective pressure for invariance, whereas, in regulatory regions several lines of evidence support the role of balancing selection. Since HLA-G has immunomodulatory properties, the understanding of gene regulation and the role of polymorphic sites on gene function may permit an individualized approach for the future use of HLA-G for therapeutic purposes.

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          Most cited references193

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          Coordinated histone modifications mediated by a CtBP co-repressor complex.

          The transcriptional co-repressor CtBP (C-terminal binding protein) is implicated in tumorigenesis because it is targeted by the adenovirus E1A protein during oncogenic transformation. Genetic studies have also identified a crucial function for CtBP in animal development. CtBP is recruited to DNA by transcription factors that contain a PXDLS motif, but the detailed molecular events after the recruitment of CtBP to DNA and the mechanism of CtBP function in tumorigenesis are largely unknown. Here we report the identification of a CtBP complex that contains the essential components for both gene targeting and coordinated histone modifications, allowing for the effective repression of genes targeted by CtBP. Inhibiting the expression of CtBP and its associated histone-modifying activities by RNA-mediated interference resulted in alterations of histone modifications at the promoter of the tumour invasion suppressor gene E-cadherin and increased promoter activity in a reporter assay. These findings identify a molecular mechanism by which CtBP mediates transcriptional repression and provide insight into CtBP participation in oncogenesis.
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            The molecular biology of the CCAAT-binding factor NF-Y.

            Protein coding genes are transcribed by Polymerase II, under the control of short discrete DNA elements in promoters and enhancers, recognized with high efficiency and specificity by trans-acting factors and by general transcription proteins (Tjian and Maniatis, 1994). The former regulate specific genes or set of genes, usually in a tissue-, developmental-, cell-cycle or stimuli-dependent way; the latter are involved in the activation of all promoters, as a whole multi-subunit holoenzyme (Parvis and Young, 1998). A limited set of elements, such as the GC and CCAAT-boxes, are present in a very high number of promoters. The whole process is further complicated by the need to operate in the context of higher order chromatin structures (Workman and Kingston, 1998). This review focuses on the CCAAT sequence and on the NF-Y protein, also known as CBF, which binds to it.
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              MHC class I antigen presentation: learning from viral evasion strategies.

              The cell surface display of peptides by MHC class I molecules to lymphocytes provides the host with an important surveillance mechanism to protect against invading pathogens. However, in turn, viruses have evolved elegant strategies to inhibit various stages of the MHC class I antigen presentation pathway and prevent the display of viral peptides. This Review highlights how the elucidation of mechanisms of viral immune evasion is important for advancing our understanding of virus-host interactions and can further our knowledge of the MHC class I presentation pathway as well as other cellular pathways.
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                Author and article information

                Contributors
                +55-16-36022566 , +55-16-36336695 , eadonadi@fmrp.usp.br
                Journal
                Cell Mol Life Sci
                Cellular and Molecular Life Sciences
                SP Birkhäuser Verlag Basel (Basel )
                1420-682X
                1420-9071
                24 November 2010
                24 November 2010
                February 2011
                : 68
                : 3
                : 369-395
                Affiliations
                [1 ]Division of Clinical Immunology, Department of Medicine, School of Medicine of Ribeirão Preto, University of São Paulo, Av. Bandeirantes, 3900, 14049-900 Ribeirão Preto, SP Brazil
                [2 ]Department of Immunology, University Complutense, The Madrid Regional Blood Center, Madrid, Spain
                [3 ]Laboratoire d’Immunogénétique, Centre de Recherche du Centre Hospitalier de l’Université de Montréal, Montreal, Canada
                [4 ]Commissariat à l’Energie Atomique/DSV/I2BM/Service de Recherches en Hémato-Immunologie, IUH, Hôpital Saint-Louis, 75010 Paris, France
                Article
                580
                10.1007/s00018-010-0580-7
                3021195
                21107637
                34dccbeb-4838-429d-a36f-24a569a78cc1
                © The Author(s) 2010
                History
                : 21 October 2010
                : 22 October 2010
                Categories
                Multi-Author Review
                Custom metadata
                © Springer Basel AG 2011

                Molecular biology
                primate evolution,chronic viral infections,mhc-g,regulation,evolution,hla-g,tumor,transplantation,autoimmunity,polymorphism

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