Transcriptional quiescence of paternal mtDNA in cyprinid fish embryos

• DOI: 10.1038/srep28571
• Publication Date: 2016-06-23T09:29:59Z
• Authors: Ming Wen; Liangyue Peng; Xinjiang Hu; Yuling Zhao; Shaojun Liu; Yunhan Hong
• Keywords: Male; 0301 basic medicine; zygote; 570; Zygote; Cyprinidae; Embryonic Development; gene regulatory network; mitochondrial DNA; DNA, Mitochondrial; Article; 03 medical and health sciences; male; mitochondrion; Animals; animal; genetics; Gene Regulatory Networks; 0303 health sciences; embryo development; DNA; Mitochondrial; Mitochondria; female; physiology; Female

AbstractMitochondrial homoplasmy signifies the existence of identical copies of mitochondrial DNA (mtDNA) and is essential for normal development, as heteroplasmy causes abnormal development and diseases in human. Homoplasmy in many organisms is ensured by maternal mtDNA inheritance through either absence of paternal mtDNA delivery or early elimination of paternal mtDNA. However, whether paternal mtDNA is transcribed has remained unknown. Here we report that paternal mtDNA shows late elimination and transcriptional quiescence in cyprinid fishes. Paternal mtDNA was present in zygotes but absent in larvae and adult organs of goldfish and blunt-snout bream, demonstrating paternal mtDNA delivery and elimination for maternal mtDNA inheritance. Surprisingly, paternal mtDNA remained detectable up to the heartbeat stage, suggesting its late elimination leading to embryonic heteroplasmy up to advanced embryogenesis. Most importantly, we never detected the cytb RNA of paternal mtDNA at all stages when paternal mtDNA was easily detectable, which reveals that paternal mtDNA is transcriptionally quiescent and thus excludes its effect on the development of heteroplasmic embryos. Therefore, paternal mtDNA in cyprinids shows late elimination and transcriptional quiescence. Clearly, transcriptional quiescence of paternal mtDNA represents a new mechanism for maternal mtDNA inheritance and provides implications for treating mitochondrion-associated diseases by mitochondrial transfer or replacement.