Woitach_1998_Nat.Genet_19_371

Reference

Title : A retinoblastoma-binding protein that affects cell-cycle control and confers transforming ability - Woitach_1998_Nat.Genet_19_371
Author(s) : Woitach JT , Zhang M , Niu CH , Thorgeirsson SS
Ref : Nat Genet , 19 :371 , 1998
Abstract :

The retinoblastoma (RB) gene is one of the most extensively studied tumour-suppressor genes. Deletion or inactivation of both RB alleles is an essential, rate-limiting step in the formation of retinoblastoma and osteosarcoma that arise in families that carry mutant RB (ref. 2). RB inactivation is also found in other human tumours. Whereas loss of RB function is associated with the loss of cellular proliferative control, introduction of a wild-type RB can suppress cell growth and tumorigenicity. Thus, identification of factors that interfere with and/or control the function of the RB protein is critical for understanding both cell-cycle control and oncogenesis. Here we describe a new gene, Bog (for B5T over-expressed gene), which was identified and shown to be overexpressed in several transformed rat liver epithelial (RLE) cell lines resistant to the growth-inhibitory effect of TGF-beta1, as well as in primary human liver tumours. The Bog protein shares homology with other retinoblastoma-binding proteins and contains the Rb-binding motif LXCXE. Using the yeast two-hybrid system and co-immunoprecipitation, we demonstrated that Bog binds to Rb. In vivo, Bog/Rb complexes do not contain E2F-1, and Bog can displace E2F-1 from E2F-1/Rb complexes in vitro. Overexpression of Bog in normal RLE cells conferred resistance to the growth-inhibitory effect of TGF-beta1. Furthermore, normal RLE cells are rapidly transformed when Bog is continuously overexpressed and form hepatoblastoma-like tumours when transplanted into nude mice. These data suggest that Bog may be important in the transformation process, in part due to its capacity to confer resistance to the growth-inhibitory effects of TGF-beta1 through interaction with Rb and the subsequent displacement of E2F-1.

PubMedSearch : Woitach_1998_Nat.Genet_19_371
PubMedID: 9697699
Gene_locus related to this paper: human-RBBP9 , ratno-rbbp9

Related information

Gene_locus human-RBBP9    ratno-rbbp9
Family human-RBBP9    ratno-rbbp9    Hydrolase_RBBP9_YdeN

Citations formats

Woitach JT, Zhang M, Niu CH, Thorgeirsson SS (1998)
A retinoblastoma-binding protein that affects cell-cycle control and confers transforming ability
Nat Genet 19 :371

Woitach JT, Zhang M, Niu CH, Thorgeirsson SS (1998)
Nat Genet 19 :371