Escape and migration of nucleic acids between chloroplasts, mitochondria, and the nucleus
- PMID: 8900960
- DOI: 10.1016/s0074-7696(08)62223-8
Escape and migration of nucleic acids between chloroplasts, mitochondria, and the nucleus
Abstract
The escape and migration of genetic information between mitochondria, chloroplasts, and nuclei have been an integral part of evolution and has a continuing impact on the biology of cells. The evolutionary transfer of functional genes and fragments of genes from chloroplasts to mitochondria, from chloroplasts to nuclei, and from mitochondria to nuclei has been documented for numerous organisms. Most documented instances of genetic material transfer have involved the transfer of information from mitochondria and chloroplasts to the nucleus. The pathways for the escape of DNA from organelles may include transient breaches in organellar membranes during fusion and/or budding processes, terminal degradation of organelles by autophagy coupled with the subsequent release of nucleic acids to the cytoplasm, illicit use of nucleic acid or protein import machinery, or fusion between heterotypic membranes. Some or all of these pathways may lead to the escape of DNA or RNA from organellar compartments with subsequent uptake of nucleic acids from the cytoplasm into the nucleus. Investigations into the escape of DNA from mitochondria in yeast have shown the rate of escape for gene-sized fragments of DNA from mitochondria and its subsequent migration to the nucleus to be roughly equivalent to the rate of spontaneous mutation of nuclear genes. Smaller fragments of mitochondrial DNA may appear in the nucleus even more frequently. Mutations of nuclear genes that define gene products important in controlling the rate of DNA escape from mitochondria in yeast also have been described. The escape of genetic material from mitochondria and chloroplasts has clearly had an impact on nuclear genetic organization throughout evolution and may also affect cellular metabolic processes.
Similar articles
-
Escape of DNA from mitochondria to the nucleus in Saccharomyces cerevisiae.Nature. 1990 Jul 26;346(6282):376-9. doi: 10.1038/346376a0. Nature. 1990. PMID: 2165219
-
Nucleic acid import into mitochondria: New insights into the translocation pathways.Biochim Biophys Acta. 2015 Dec;1853(12):3165-81. doi: 10.1016/j.bbamcr.2015.09.011. Epub 2015 Sep 12. Biochim Biophys Acta. 2015. PMID: 26376423
-
Pervasive migration of organellar DNA to the nucleus in plants.J Mol Evol. 1995 Oct;41(4):397-406. doi: 10.1007/BF00160310. J Mol Evol. 1995. PMID: 7563126
-
The co-ordination of nuclear and organellar genome expression in eukaryotic cells.Essays Biochem. 1997;32:113-25. Essays Biochem. 1997. PMID: 9493015 Review.
-
Role of intercompartmental DNA transfer in producing genetic diversity.Int Rev Cell Mol Biol. 2011;291:73-114. doi: 10.1016/B978-0-12-386035-4.00003-3. Int Rev Cell Mol Biol. 2011. PMID: 22017974 Review.
Cited by
-
Assigning mitochondrial localization of dual localized proteins using a yeast Bi-Genomic Mitochondrial-Split-GFP.Elife. 2020 Jul 13;9:e56649. doi: 10.7554/eLife.56649. Elife. 2020. PMID: 32657755 Free PMC article.
-
Cab gene expression in bleached leaves of carotenoid-deficient maize.Photosynth Res. 2000;64(2-3):119-26. doi: 10.1023/A:1006477215572. Photosynth Res. 2000. PMID: 16228450
-
Genetical and molecular analysis reveals a cooperating relationship between cytoplasmic male sterility- and fertility restoration-related genes in Oryza species.Theor Appl Genet. 2011 Jan;122(1):9-19. doi: 10.1007/s00122-010-1418-2. Epub 2010 Aug 17. Theor Appl Genet. 2011. PMID: 20714705
-
Mitochondria in the Nuclei of Rat Myocardial Cells.Cells. 2020 Mar 14;9(3):712. doi: 10.3390/cells9030712. Cells. 2020. PMID: 32183238 Free PMC article.
-
Molecular poltergeists: mitochondrial DNA copies (numts) in sequenced nuclear genomes.PLoS Genet. 2010 Feb 12;6(2):e1000834. doi: 10.1371/journal.pgen.1000834. PLoS Genet. 2010. PMID: 20168995 Free PMC article.