Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Mar;362(1-2):249-62.
doi: 10.1007/s11010-011-1150-5. Epub 2011 Dec 3.

De-regulation of the RBBP6 isoform 3/DWNN in human cancers

Affiliations

De-regulation of the RBBP6 isoform 3/DWNN in human cancers

Zukile Mbita et al. Mol Cell Biochem. 2012 Mar.

Abstract

Retinoblastoma binding protein 6 (RBBP6) is a nuclear protein, previously implicated in the regulation of cell cycle and apoptosis. The human RBBP6 gene codes for three protein isoforms and isoform 3 consists of the domain with no name domain only whilst the other two isoforms, 1 and 2 comprise of additional zinc, RING, retinoblastoma and p53 binding domains. In this study, the localization of RBBP6 using RBBP6 variant 3 mRNA-specific probe was performed to investigate the expression levels of the gene in different tumours and find a link between RBBP6 and human carcinogenesis. Using FISH, real-time PCR and Western blotting analysis our results show that RBBP6 isoform 3 is down-regulated in human cancers. RBBP6 isoform 3 knock-down resulted in reduced G2/M cell cycle arrest whilst its over-expression resulted in increased G2/M cell cycle arrest using propidium iodide DNA staining. The results further demonstrate that the RBBP6 isoform 3 may be the cell cycle regulator and involved in mitotic apoptosis not the isoform 1 as previously reported for mice. In conclusion, these findings suggest that RBBP6 isoform 3 is a cell cycle regulator and may be de-regulated in carcinogenesis.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Immunol Methods. 1987 Apr 16;98(2):249-55 - PubMed
    1. J Cell Biochem. 2003 Sep 1;90(1):6-12 - PubMed
    1. J Cell Physiol. 2002 May;191(2):145-54 - PubMed
    1. Oncogene. 1997 Jan 16;14(2):145-55 - PubMed
    1. Clin Cancer Res. 2004 Oct 1;10(19):6437-48 - PubMed

Publication types

MeSH terms

LinkOut - more resources