Truncated forms of BNIP3 act as dominant negatives inhibiting hypoxia-induced cell death

• Published in: Biochimica et biophysica acta Vol. 1812; no. 3; pp. 302 - 311
• Main Authors: Bristow, Nicolle, Burton, Teralee R., Henson, Elizabeth S., Ong-Justiniano, Coleen, Brown, Michelle, Gibson, Spencer B.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01-03-2011
• Subjects: Animals; Apoptosis; Bcl-2 family; Blotting, Western; BNIP3; Cell death and cancer; Cell Proliferation; Cell Survival - physiology; Cells, Cultured; Fluorescent Antibody Technique; Genes, Dominant; Humans; Hypoxia; Hypoxia - metabolism; Hypoxia - prevention & control; Immunoenzyme Techniques; Membrane Proteins - chemistry; Membrane Proteins - physiology; Mice; Mitochondria - metabolism; Mutation - genetics; Neoplasms - metabolism; Neoplasms - pathology; Normoxia; Proto-Oncogene Proteins - chemistry; Proto-Oncogene Proteins - physiology; Transfection; Tumor Cells, Cultured; Normoxia; Cell death and cancer; Hypoxia; BNIP3; Bcl-2 family
• ISSN: 0925-4439; 0006-3002; 1879-260X
• DOI: 10.1016/j.bbadis.2010.11.013

BNIP3 (
Bcl-2/adenovirus E1B
Nineteen Kilodalton
Interacting
Protein) is a pro-cell death member of the Bcl-2 family of proteins. Its expression is induced by the transcription factor Hypoxia Inducible Factor-1 (HIF-1) under conditions of low oxygen (hypoxia) and is found over expressed in hypoxic regions of many tumors. When over expressed, BNIP3 induces cell death through induction of mitochondrial dysfunction that is dependent on the presence of BNIP3's TM domain. Herein, we have determined that the SkOv3 ovarian cancer cell line expresses a truncated BNIP3 protein, which results in the elimination of the transmembrane domain. Truncation that eliminates all four domains of BNIP3 protein also inhibits hypoxia-induced cell death in SkOv3, HEK293, U251 and MCF-7 cells. Three different mutations in a BNIP3 expression vector that lead to a truncated BNIP3 protein, lacking TM domain only, or lacking CD, BH3, and TM domains resulted in inhibition of hypoxia-induced cell death when transfected into HEK293 cells. We found that truncated BNIP3 failed to associate with the mitochondria and the truncated BNIP3 lacking all four domains can bind to wild type BNIP3. Taken together, truncation of BNIP3 could be a novel mechanism for cancer cells to avoid hypoxia-induced cell death mediated by BNIP3 over expression.
► Truncated BNIP3 lacks all four domains found in the wild type protein. ► Truncated BNIP3 protein inhibits hypoxia-induced cell death. ► Truncated BNIP3 failed to associate with the mitochondria. ► Truncated BNIP3 lacking all four domains can bind to wild type BNIP3. ► Truncated BNIP3 can prevent wild type BNIP3 localization to the mitochondria.