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Isolation and characterization of a membrane-DNA complex in the mitochondria of Physarum polycephalum
Abstract:
A membrane-DNA complex was isolated by centrifugation of sheared lysate of isolated mitochondria in 20-60% sucrose step solution. Analyses using Hoechst 33258/CsCl density gradient centrifugation and restriction endonuclease treatment showed that DNA in the membrane-DNA complex was AT-rich compared with total mitochondrial DNA (mt DNA) and contained Eco RI fragments of E-4, 5 and 8, which were localized on the right hand of Physarum mitochondrial genome. Phenethyl alcohol (PEA) and ethidium bromide (EB) could disrupt the membrane-DNA complex to release DNA fragments from their complex in vitro. Addition of 0.5% or more PEA, which released 80-90% of the DNA from the membrane-DNA complex in vitro, inhibited not only mitochondrial nuclear division but also mitochondrial division in vivo. EB treatment at more than 1 mg/ml disrupted the membrane-DNA complex in vitro to release 77% of the total DNA in the complex. Addition of 10 micrograms/ml EB induced unequal mitochondrial nuclear division in the microplasmodia, e.g., a dividing dumbbell-shaped mitochondrion had the mt-nucleus in one side and as a result formed then one nucleated and one enucleated mitochondrion. From the EB-pretreated mitochondria, a lesser amount of the membrane-DNA complex was isolated than from the control. These findings mean than the unequal mt-nuclear division is due to dissociation of DNA and the membrane system in the membrane-DNA complex. They strongly suggested that the DNA region (E-4, 5 and 8), where the mitochondrial nucleus is associated with the mitochondrial membrane system plays an important role in mitochondrial nuclear division.
Insights
Mitochondrial DNA (mtDNA) in a membrane-DNA complex plays a key role in cell division. Disrupting this complex with chemicals like PEA or EB causes abnormal mitochondrial nuclear division.
Area of Science:
- Mitochondrial biology
- Molecular genetics
- Cell division
Background:
- Mitochondria possess their own DNA (mtDNA) and play crucial roles in cellular energy production and division.
- The association of mtDNA with mitochondrial membranes is implicated in mtDNA replication and segregation during cell division.
Purpose of the Study:
- To investigate the role of the membrane-DNA complex in mitochondrial nuclear division.
- To identify specific mtDNA regions involved in this process.
Main Methods:
- Isolation of membrane-DNA complexes from mitochondria using sucrose density gradients.
- Analysis of DNA composition using Hoechst 33258/CsCl density gradients and restriction endonuclease digestion.
- Treatment with phenethyl alcohol (PEA) and ethidium bromide (EB) to disrupt the complex in vitro and in vivo.
Main Results:
- The membrane-DNA complex contains AT-rich mtDNA, including Eco RI fragments E-4, 5, and 8, localized on the right side of the Physarum mitochondrial genome.
- PEA and EB disrupt the membrane-DNA complex, releasing mtDNA fragments.
- In vivo treatment with PEA inhibits mitochondrial division, while EB induces unequal mitochondrial nuclear division, suggesting dissociation of DNA from the membrane system.
Conclusions:
- The membrane-DNA complex, particularly the association of mtDNA regions E-4, 5, and 8 with the mitochondrial membrane, is crucial for proper mitochondrial nuclear division.
- Disruption of this complex leads to aberrant mitochondrial division.
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