Singh Bhupendra, Li Xiurong, Owens Kjerstin M, Vanniarajan Ayyasamy, Liang Ping, Singh Keshav K
Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
PLoS One. 2015 Oct 13;10(10):e0140409. doi: 10.1371/journal.pone.0140409. eCollection 2015.
To date, mitochondrial DNA polymerase γ (POLG) is the only polymerase known to be present in mammalian mitochondria. A dogma in the mitochondria field is that there is no other polymerase present in the mitochondria of mammalian cells. Here we demonstrate localization of REV3 DNA polymerase in the mammalian mitochondria. We demonstrate localization of REV3 in the mitochondria of mammalian tissue as well as cell lines. REV3 associates with POLG and mitochondrial DNA and protects the mitochondrial genome from DNA damage. Inactivation of Rev3 leads to reduced mitochondrial membrane potential, reduced OXPHOS activity, and increased glucose consumption. Conversely, inhibition of the OXPHOS increases expression of Rev3. Rev3 expression is increased in human primary breast tumors and breast cancer cell lines. Inactivation of Rev3 decreases cell migration and invasion, and localization of Rev3 in mitochondria increases survival and the invasive potential of cancer cells. Taken together, we demonstrate that REV3 functions in mammalian mitochondria and that mitochondrial REV3 is associated with the tumorigenic potential of cells.
迄今为止,线粒体DNA聚合酶γ(POLG)是已知存在于哺乳动物线粒体中的唯一聚合酶。线粒体领域的一个教条是,哺乳动物细胞的线粒体中不存在其他聚合酶。在此,我们证明了REV3 DNA聚合酶在哺乳动物线粒体中的定位。我们证明了REV3在哺乳动物组织以及细胞系的线粒体中的定位。REV3与POLG和线粒体DNA相关联,并保护线粒体基因组免受DNA损伤。Rev3的失活导致线粒体膜电位降低、氧化磷酸化(OXPHOS)活性降低以及葡萄糖消耗增加。相反,抑制OXPHOS会增加Rev3的表达。Rev3在人类原发性乳腺肿瘤和乳腺癌细胞系中的表达增加。Rev3的失活会降低细胞迁移和侵袭能力,而Rev3在线粒体中的定位会增加癌细胞的存活率和侵袭潜力。综上所述,我们证明了REV3在哺乳动物线粒体中发挥作用,并且线粒体REV3与细胞的致瘤潜力相关。