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Regulatory cis- and trans-elements of mitochondrial D-loop-driven reporter genes in budding tunicates.

作者信息

Kawamura Kaz, Saitoh Yuhya, Ballarin Loriano, Sunanaga Takeshi

机构信息

Laboratory of Cellular and Molecular Biotechnology, Faculty of Science, Kochi University, Kochi, Japan.

Laboratory of Cellular and Molecular Biotechnology, Faculty of Science, Kochi University, Kochi, Japan.

出版信息

Mitochondrion. 2017 Jul;35:59-69. doi: 10.1016/j.mito.2017.05.006. Epub 2017 May 17.

Abstract

To unveil the underlying mechanism of mitochondrial gene regulation associated with ageing and budding in the tunicate Polyandrocarpa misakiensis, mitochondrial non-coding-region (NCR)-containing reporter genes were constructed. PmNCR2.3K/GFP was expressed spatiotemporally in a pattern quite similar to mitochondrial 16SrRNA. The reporter gene expression was sensitive to high dose of rifampicin similar to mitochondrial genes, suggesting that the transcription indeed occurs in mitochondria. However, the gene expression also occurred in vivo in the cell nucleus and in vitro in the nuclear extracts. Mitochondrial transcription factor A (PmTFAM) enhanced reporter gene expression, depending on the NCR length. A budding-specific polypeptide TC14-3 is an epigenetic histone methylation inducer. It heavily enhanced reporter gene expression that was interfered by histone methylation inhibitors and PmTFAM RNAi. Our results indicate for the first time that the nuclear histone methylation is involved in mitochondrial gene activity via TFAM gene regulation.

摘要

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