Conserved region 2 of adenovirus E1A has a function distinct from pRb binding required to prevent cell cycle arrest by p16 super(INK4a) or p27 super(Kip1)

• Published in: Oncogene Vol. 19; no. 16; pp. 2067 - 2074
• Main Authors: Alevizopoulos, K, Sanchez, B, Amati, B
• Format: Journal Article
• Language: English
• Published: 13.04.2000
• Subjects: adeno-associated virus; Adenovirus; E1A protein; INK4a gene; p16 protein; p16@uINK4a protein; p27 protein; p27@uKip1 protein; RB protein
• ISSN: 0950-9232

Ectopic expression of the CDK inhibitors (CKIs) p16 super(INK4a) and p27 super(Kip1) in Rat1 fibroblasts induces dephosphorylation and activation of Retinoblastoma-family proteins (pRb, p107 and p130), their association with E2F proteins, and cell cycle arrest in G1. The growth-inhibitory action of p16, in particular, is believed to be mediated essentially via pRb activation. The 12S E1A protein of human Adenovirus 5 associates with pRb-family proteins via residues in its Conserved Regions (CR) 1 and 2, in particular through the motif LXCXE in CR2. These interactions are required for E1A to prevent G1 arrest upon co-expression of CKIs. We show here that mutating either of two conserved motifs adjacent to LXCXE in CR2, GFP and SDDEDEE, also impairs the ability of E1A to overcome G1 arrest by p16 or p27. Strikingly, however, these mutations affect neither the association of E1A with pRb, p07 and p130, nor its ability to derepress E2F-1 transcriptional activity in transient transfection assays. One of the E1A mutants, however, is defective in derepressing several endogenous E2F target genes in the presence of p16 or p27. Thus, CR2 possesses an essential function besides pRb-binding. We speculate that this function might be required for the full derepression of E2F-regulated genes in their natural chromatin context.