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1.
PLoS One ; 7(8): e42106, 2012.
Article in English | MEDLINE | ID: mdl-22879910

ABSTRACT

The Epstein-Barr Virus (EBV) -encoded EBNA2 protein, which is essential for the in vitro transformation of B-lymphocytes, interferes with cellular processes by binding to proteins via conserved sequence motifs. Its Arginine-Glycine (RG) repeat element contains either symmetrically or asymmetrically di-methylated arginine residues (SDMA and ADMA, respectively). EBNA2 binds via its SDMA-modified RG-repeat to the survival motor neurons protein (SMN) and via the ADMA-RG-repeat to the NP9 protein of the human endogenous retrovirus K (HERV-K (HML-2) Type 1). The hypothesis of this work was that the methylated RG-repeat mimics an epitope shared with cellular proteins that is used for interaction with target structures. With monoclonal antibodies against the modified RG-repeat, we indeed identified cellular homologues that apparently have the same surface structure as methylated EBNA2. With the SDMA-specific antibodies, we precipitated the Sm protein D3 (SmD3) which, like EBNA2, binds via its SDMA-modified RG-repeat to SMN. With the ADMA-specific antibodies, we precipitated the heterogeneous ribonucleoprotein K (hnRNP K). Specific binding of the ADMA- antibody to hnRNP K was demonstrated using E. coli expressed/ADMA-methylated hnRNP K. In addition, we show that EBNA2 and hnRNP K form a complex in EBV- infected B-cells. Finally, hnRNP K, when co-expressed with EBNA2, strongly enhances viral latent membrane protein 2A (LMP2A) expression by an unknown mechanism as we did not detect a direct association of hnRNP K with DNA-bound EBNA2 in gel shift experiments. Our data support the notion that the methylated surface of EBNA2 mimics the surface structure of cellular proteins to interfere with or co-opt their functional properties.


Subject(s)
Epstein-Barr Virus Nuclear Antigens/metabolism , Heterogeneous-Nuclear Ribonucleoprotein K/metabolism , Viral Matrix Proteins/metabolism , Viral Proteins/metabolism , Antibodies, Monoclonal/immunology , Antibody Specificity/immunology , Arginine/analogs & derivatives , Arginine/metabolism , Cell Line , DNA/metabolism , Epstein-Barr Virus Infections/metabolism , Epstein-Barr Virus Nuclear Antigens/chemistry , Epstein-Barr Virus Nuclear Antigens/immunology , Gene Expression Regulation, Viral , Herpesvirus 4, Human/genetics , Herpesvirus 4, Human/physiology , Humans , Immunoprecipitation , Methylation , Molecular Sequence Data , Multiprotein Complexes/metabolism , Mutant Proteins/metabolism , Promoter Regions, Genetic/genetics , Protein Binding , Protein Transport , Repetitive Sequences, Amino Acid , Transfection , Viral Matrix Proteins/genetics , Viral Proteins/chemistry , Viral Proteins/immunology , snRNP Core Proteins/metabolism
2.
Virology ; 397(2): 299-310, 2010 Feb 20.
Article in English | MEDLINE | ID: mdl-19969318

ABSTRACT

The Epstein-Barr virus (EBV) growth-transforms B-lymphocytes. The virus-encoded nuclear antigen 2 (EBNA2) is essential for transformation and activates gene expression by association with DNA-bound transcription factors such as RBPJkappa (CSL/CBF1). We have previously shown that EBNA2 contains symmetrically dimethylated Arginine (sDMA) residues. Deletion of the RG-repeat results in a reduced ability of the virus to immortalise B-cells. We now show that the RG repeat also contains asymmetrically dimethylated Arginines (aDMA) but neither non-methylated (NMA) Arginines nor citrulline residues. We demonstrate that only aDMA-containing EBNA2 is found in a complex with DNA-bound RBPJkappa in vitro and preferentially associates with the EBNA2-responsive EBV C, LMP1 and LMP2A promoters in vivo. Inhibition of methylation in EBV-infected cells results in reduced expression of the EBNA2-regulated viral gene LMP1, providing additional evidence that methylation is a prerequisite for DNA-binding by EBNA2 via association with the transcription factor RBPJkappa.


Subject(s)
Arginine/metabolism , DNA/metabolism , Epstein-Barr Virus Nuclear Antigens/metabolism , Herpesvirus 4, Human/physiology , Immunoglobulin J Recombination Signal Sequence-Binding Protein/metabolism , Promoter Regions, Genetic , Viral Proteins/metabolism , Animals , Cell Line , Gene Expression , Humans , Methylation , Mice , Mice, Inbred BALB C , Protein Binding , Rats , Viral Matrix Proteins/biosynthesis
3.
Blood ; 110(8): 2931-9, 2007 Oct 15.
Article in English | MEDLINE | ID: mdl-17626842

ABSTRACT

Cell-based immunotherapy in settings of allogeneic stem cell transplantation or donor leukocyte infusion has curative potential, especially in hematologic malignancies. However, this approach is severely restricted due to graft-versus-host disease (GvHD). This limitation may be overcome if target antigens are molecularly defined and effector cells are specifically selected. We chose formin-related protein in leukocytes 1 (FMNL1) as a target antigen after intensive investigation of its expression profile at the mRNA and protein levels. Here, we confirm restricted expression in peripheral blood mononuclear cells (PBMCs) from healthy donors but also observe overexpression in different leukemias and aberrant expression in transformed cell lines derived from solid tumors. We isolated allorestricted T-cell clones expressing a single defined TCR recognizing a particular HLA-A2-presented peptide derived from FMNL1. This T-cell clone showed potent antitumor activity against lymphoma and renal cell carcinoma cell lines, Epstein-Barr virus (EBV)-transformed B cells, and primary tumor samples derived from patients with chronic lymphocytic leukemia (CLL), whereas nontransformed cells with the exception of activated B cells were only marginally recognized. Allorestricted TCRs with specificity for naturally presented FMNL1-derived epitopes may represent promising reagents for the development of adoptive therapies in lymphoma and other malignant diseases.


Subject(s)
Cytoskeletal Proteins/immunology , Cytotoxicity, Immunologic , Hematologic Neoplasms/immunology , T-Lymphocytes, Cytotoxic/immunology , Antigens, Neoplasm/immunology , Blotting, Western , Bone Marrow/metabolism , Cell Line, Tumor , Clone Cells , Cytoskeletal Proteins/metabolism , Enzyme-Linked Immunosorbent Assay , Epitopes, T-Lymphocyte/immunology , Formins , HLA-A Antigens , Humans , Immunotherapy, Adoptive/methods , Leukocytes, Mononuclear/metabolism , Peptides/immunology , Receptors, Antigen, T-Cell/genetics , Reverse Transcriptase Polymerase Chain Reaction , Thymus Gland/metabolism
4.
Gene Expr Patterns ; 5(3): 341-7, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15661639

ABSTRACT

Because of its oncogenic capacity and expression restricted to embryonic and newborn tissues, the N-myc proto-oncogene is suggested to play a key role in vertebrate organogenesis as well as in the control of cell proliferation and differentiation. To further approach the developmental function of N-myc, we cloned full-length zebrafish N-myc (nmyc1) and analyzed its expression in the embryo and early larva. nmyc1 transcription is initiated at the mid-blastula stage. At somitogenesis stages, its expression was detected in the retina, midbrain, posterior hindbrain and presumptive spinal cord. nmyc1 was also transcribed in the endoderm and its derivatives as well as in branchial arches. At later developmental stages, posterior neural expression of nmyc1 was switched off, but expression remained intense in the brain, mainly in the optic tectum, cerebellar plate and dorsal rhombomere 2. Comparison of nmyc1 transcription with proliferation zones using a M phase mitotic marker revealed that nmyc1 expression is specifically associated with mitosis in the optic tectum and the retina. This result contrasts with previous studies in other vertebrates where N-myc expression can persist in differentiating cells.


Subject(s)
Genes, myc , Proto-Oncogene Proteins/biosynthesis , Retina/growth & development , Superior Colliculi/growth & development , Transcription, Genetic , Zebrafish Proteins/biosynthesis , Zebrafish/growth & development , Amino Acid Sequence , Animals , Base Sequence , Larva/growth & development , Larva/metabolism , Mitosis , Molecular Sequence Data , Proto-Oncogene Proteins/chemistry , Proto-Oncogene Proteins/genetics , Retina/embryology , Retina/metabolism , Superior Colliculi/embryology , Superior Colliculi/metabolism , Zebrafish/embryology , Zebrafish/genetics , Zebrafish/metabolism , Zebrafish Proteins/chemistry , Zebrafish Proteins/genetics
5.
Gene Expr Patterns ; 5(1): 91-6, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15533823

ABSTRACT

The VAT-1 protein is present in the electric organ of marine rays where it is suggested to play a central role in nerve signal transmission. VAT-1 homolog protein was also identified in mouse and human but its function remains to be determined. We have investigated VAT-1 homolog in zebrafish Danio rerio since it is an excellent model amenable to the combination of genetic, molecular and embryological studies. Amino acid sequence analysis shows that the zebrafish VAT-1 homolog shares approximately 51-61% identity with the electric ray, mouse, and human counterparts. By in situ hybridization, vat-1 homolog mRNA is first observed in the trigeminal nuclei at the 8-somite stage. At 20-somite stage, vat-1 homolog is detected in the brain, namely in primary clusters of neurons, in the epiphysis and in the hindbrain. vat-1 homolog is also present in the neural tube but this expression disappears after 72 h post-fertilization. At 24 h post-fertilization, vat-1 homolog starts to be expressed in the developing gut. At later stages, vat-1 homolog is present throughout the brain, appears in the maturing retina and the pharyngeal cavity.


Subject(s)
Adenosine Triphosphatases/genetics , Zebrafish Proteins/genetics , Zebrafish/genetics , Adenosine Triphosphatases/biosynthesis , Amino Acid Sequence , Animals , Base Sequence , Brain/embryology , Brain/metabolism , Branchial Region/embryology , Branchial Region/metabolism , Gene Expression Profiling , Humans , Mice , Molecular Sequence Data , Retina/embryology , Retina/metabolism , Sequence Alignment , Zebrafish/embryology , Zebrafish/metabolism , Zebrafish Proteins/biosynthesis
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