Abstract
Previous molecular genetic analyses of Epstein-Barr virus nuclear protein 2 (EBNA2) identified a negative effect of deletion of codons 19 to 33 on transformation and gene transactivation, while deletion of codons 19 to 110 was a null mutation for transformation and gene transactivation. We here report the surprising finding that codons 2 to 88, which encode the highly conserved unique N terminus (amino acids 1 to 58) and most of the polyproline repeat (amino acids 59 to 95), can be deleted with only minimal effects on transformation. Codons 97 to 122 can also be deleted with only minimal effects on transformation. However, deletion of 35 of the 37 prolines (amino acids 59 to 93) or deletion of codons 2 to 95 results in a null transforming phenotype. Although EBNA2 from which codons 59 to 93 were deleted was a null mutation for transformation, it was similar to some transforming mutants of EBNA2 in abundance, in interaction with RBPJK, and in transactivation of the LMP1 promoter in transient transfection assays. These data indicate that between three and seven prolines are critical for EBNA2 structure or for intermolecular interaction. Aside from these seven prolines, codons encoding the rest of the N-terminal half (amino acids 2 to 230) of EBNA2 are nonessential for primary B-lymphocyte growth transformation.
MeSH Terms
Antigens, Viral/genetics,physiology
B-Lymphocytes/cytology,virology
Base Sequence
Cell Line
Cell Transformation, Viral/genetics
Codon
Conserved Sequence
DNA, Viral
DNA-Binding Proteins/genetics,physiology
Epstein-Barr Virus Nuclear Antigens
Herpesvirus 4, Human/genetics,physiology
Molecular Sequence Data
Proline/physiology
Sequence Deletion
Tumor Cells, Cultured
Viral Matrix Proteins/biosynthesis
Chemicals
Antigens, Viral
Codon
DNA, Viral
DNA-Binding Proteins
EBV-associated membrane antigen, Epstein-Barr virus
Epstein-Barr Virus Nuclear Antigens
Viral Matrix Proteins
Proline
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Yalamanchili R
Department of Microbiology and Molecular Genetics, Harvard University, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
Harada S
Kieff E
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