| Literature DB >> 19540835 |
Ha-Na Woo1, Young-Woo Seo, Ae Ran Moon, Seon-Yong Jeong, Seong-Yun Jeong, Eun Kyung Choi, Tae-Hyoung Kim.
Abstract
Mitochondria form reticular networks comprised of filamentous tubules and continuously move and change shape. Bcl-2 family proteins actively participate in the regulation of mitochondria fragmentation. Here, we show that human Noxa, which belongs to the BH3-only pro-apoptotic Bcl-2 family, causes mitochondrial fragmentation. We found that while the Bcl-2 homology 3 (BH3) domain of Noxa is not associated with mitochondrial fragmentation, the mitochondrial targeting domain (MTD) of Noxa is the region responsible for inducing fragmentation. Two leucine residues in MTD play a key role in the process. Furthermore, the lack of Noxa causes a significant reduction of Velcade-induced mitochondrial fragmentation. Together, these results provide novel insight into the role of Noxa in mitochondrial dynamics and cell death.Entities:
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Year: 2009 PMID: 19540835 DOI: 10.1016/j.febslet.2009.06.029
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124