| Literature DB >> 10843669 |
X Ling1, S Kamangar, M L Boytim, Z Kelman, P Huie, S C Lyu, R K Sibley, J Hurwitz, C Clayberger, A M Krensky.
Abstract
Synthetic peptides corresponding to structural regions of HLA molecules are novel immunosuppressive agents. A peptide corresponding to residues 65-79 of the alpha-chain of HLA-DQA03011 (DQ65-79) blocks cell cycle progression from early G1 to the G1 restriction point, which inhibits cyclin-dependent kinase-2 activity and phosphorylation of the retinoblastoma protein. A yeast two-hybrid screen identified proliferating cell nuclear Ag (PCNA) as a cellular ligand for this peptide, whose interaction with PCNA was further confirmed by in vitro biochemistry. Electron microscopy demonstrates that the DQ65-79 peptide enters the cell and colocalizes with PCNA in the T cell nucleus in vivo. Binding of the DQ65-79 peptide to PCNA did not block polymerase delta (pol delta)-dependent DNA replication in vitro. These findings support a key role for PCNA as a sensor of cell cycle progression and reveal an unanticipated function for conserved regions of HLA molecules.Entities:
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Year: 2000 PMID: 10843669 DOI: 10.4049/jimmunol.164.12.6188
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422