AI Article Synopsis

  • Mitochondrial nucleoids from mung bean seedlings show a chromatin-like structure, sharing phospholipids and proteins with intact mitochondria and consistently associated with actin.
  • These nucleoids can direct DNA synthesis and exhibit distinct behaviors during mtDNA synthesis, indicating the presence of a specific gamma-type DNA polymerase.
  • The findings suggest that mitochondrial nucleoids play a crucial role beyond just organizing mtDNA, acting as centers for its maintenance and expression in eukaryotic cells.

Article Abstract

Mitochondrial nucleoids isolated from mung bean seedlings exhibited a chromatin-like structure associated with a membrane component. A similar structure, which underwent discrete changes during cotyledon development, was identified in situ. Isolated nucleoids consisted of essentially the same phospholipids, including cardiolipin, as whole mitochondria and proteins of inner- and outer-mitochondrial-membrane origin. Actin was consistently found with mitochondrial nucleoids prepared with different detergent concentrations. Formaldehyde cross-linking of cytochalasin B- and proteinase K-treated mitochondria further revealed that actin was associated with DNA in nucleoids. Mitochondrial nucleoids were self-sufficient in directing DNA synthesis in vitro in a pattern mimicking mtDNA synthesis in isolated mitochondria. In pulse-field gel electrophoresis, newly synthesized mtDNA separated into two major components, well-bound and fast-moving forms. Nucleoids DNA synthesis was resistant to aphidicolin but sensitive to N-ethylmaleimide, which indicates that a gamma-type DNA polymerase was responsible for this activity. Mitochondrial nucleoids were capable of self-directed RNA transcription in a non-random fashion in vitro. Consistent with and complementary to results from fungi and human cells done mostly in situ, our present work helps to establish the important paradigm that mitochondrial nucleoids in eukaryotes are more than mere mtDNA compaction and segregation entities but are centers of mtDNA maintenance and expression.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1188516PMC
http://dx.doi.org/10.1093/nar/gki783DOI Listing

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