Interaction theory of mammalian mitochondria

Biochemical and Biophysical Research Communications

Volumn 288, Issue 4, 2001, Pages 743-746

  Nakada, Kazuto ^a   Inoue, Kimiko ^b   Hayashi, Jun Ichi ^a  

^a UNIVERSITY OF TSUKUBA   (Japan)

^b NATIONAL INSTITUTE OF INFECTIOUS DISEASES   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

BIOGENESIS; DELETION MUTANT; EMBRYO DEVELOPMENT; INDIVIDUALITY; MAMMAL CELL; MITOCHONDRION; MOLECULAR INTERACTION; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; REVIEW; SOMATIC CELL; THEORY; ZYGOTE;

MAMMALIA;

EID: 0035834553     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.2001.5838     Document Type: Article

References (22)

1. Molecular genetic aspects of human mitochondrial disorders
2. Mitochondrial diseases in man and mouse
3. Isolation of mitochondrial DNA-less mouse cell lines and their application for trapping mouse synaptosomal mitochondrial DNA with deletion mutations
4. Isolation and characterization of mitochondrial DNA-less lines from various mammalian cell lines by application of an anticancer drug, ditercalinium
5. Complete repopulation of mouse mitochondrial DNA-less cells with rat mitochondrial DNA restores mitochondrial translation but not mitochondrial respiratory function
6. Mice with only rat mtDNA is required as models of mitochondrial diseases
7. Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes
8. Selective elimination of paternal mitochondrial DNA during mouse embryogenesis
9. Selective and continuous elimination of mitochondria microinjected into mouse eggs from spermatids, but not from liver cells, occurs throughout embryogenesis
10. Intermitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA
11. Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell with distinct organelles
12. Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells
13. The interorganellar interaction between distinct human mitochondria with deletion mutant mtDNA from a patient with mitochondrial disease and with HeLa mtDNA
14. Transcomplementation between different types of respiration-deficient mitochondria with different pathogenic mutant mitochondrial DNAs
15. Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria
16. Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
17. Human mitochondria and mitochondrial genome function as a single dynamic cellular unit
18. Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases
19. Mitochondrial genetics: A paradigm for aging and degenerative diseases?
20. Ageing and mammalian mitochondrial genetics
21. Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from aged patients with Alzheimer's disease
22. Nuclear-recessive mutations of factors involved in mitochondrial translation are responsible for age-related respiration deficiency of human skin fibroblasts