Selection by drug resistance proteins located in the mitochondria of mammalian cells

Mitochondrion

Volumn 8, Issue 5-6, 2008, Pages 345-351

  Yoon, Young Geol ^a,b   Koob, Michael D ^a,b  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

Author keywords

Drug resistance proteins; Mitochondria; mtDNA; Selectable markers

Indexed keywords

ANTIBIOTIC G 418; GREEN FLUORESCENT PROTEIN; HYGROMYCIN; HYGROMYCIN PHOSPHOTRANSFERASE; KANAMYCIN KINASE; PHOSPHOTRANSFERASE; UNCLASSIFIED DRUG;

ARTICLE; CELL VIABILITY; CELLULAR DISTRIBUTION; CONTROLLED STUDY; GENETIC ENGINEERING; HUMAN; HUMAN CELL; MITOCHONDRIAL GENETICS; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; WESTERN BLOTTING;

CELL PROLIFERATION; CINNAMATES; DRUG RESISTANCE; GENTAMICINS; HELA CELLS; HUMANS; HYGROMYCIN B; KANAMYCIN KINASE; MITOCHONDRIA; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); RECOMBINANT FUSION PROTEINS;

MAMMALIA;

EID: 54949101085     PISSN: 15677249     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mito.2008.07.004     Document Type: Article

References (37)

1. Bagger-Sjoback D., and Wersall J. Gentamicin-induced mitochondrial damage in inner ear sensory cells of the lizard calotes versicolor. Acta Otolaryngol. 86 (1978) 35-51
2. Beck E., Ludwig G., Auerswald E.A., Reiss B., and Schaller H. Nucleotide sequence and exact localization of the neomycin phosphotransferase gene from transposon Tn5. Gene 19 (1982) 327-336
3. Boynton J.E., and Gillham N.W. Genetics and transformation of mitochondria in the green alga Chlamydomonas. Methods Enzymol. 264 (1996) 279-296
4. Butow R.A., Henke R.M., Moran J.V., Belcher S.M., and Perlman P.S. Transformation of Saccharomyces cerevisiae mitochondria using the biolistic gun. Methods Enzymol. 264 (1996) 265-278
5. Davies J., Gorini L., and Davis B.D. Misreading of RNA codewords induced by aminoglycoside antibiotics. Mol. Pharmacol. 1 (1965) 93-106
6. Duvall A.J., and Wersaell J. Site of action of streptomycin upon inner ear sensory cells. Acta Otolaryngol. 57 (1964) 581-598
7. de Groot J.C., Meeuwsen F., Ruizendaal W.E., and Veldman J.E. Ultrastructural localization of gentamicin in the cochlea. Hear. Res. 50 (1990) 35-42
8. Epler J.L., Shugart L.R., and Barnett W.E. N-formylmethionyl transfer ribonucleic acid in mitochondria from Neurospora. Biochemistry 9 (1970) 3575-3579
9. Fox T.D., Sanford J.C., and McMullin T.W. Plasmids can stably transform yeast mitochondria lacking endogenous mtDNA. Proc. Natl. Acad. Sci. USA 85 (1988) 7288-7292
10. Gaines III G.L. In organello RNA synthesis system from HeLa cells. Methods Enzymol. 264 (1996) 43-49
11. Galper J.B., and Darnell J.E. The presence of N-formyl-methionyl-tRNA in HeLa cell mitochondria. Biochem. Biophys. Res. Commun. 34 (1969) 205-214
12. Golik P., Bonnefoy N., Szczepanek T., Saint-Georges Y., and Lazowska J. The Rieske FeS protein encoded and synthesized within mitochondria complements a deficiency in the nuclear gene. Proc. Natl. Acad. Sci. USA 100 (2003) 8844-8849
13. Gutell R.R. Collection of small subunit (16S- and 16S-like) ribosomal RNA structures: 1994. Nucleic Acids Res. 22 (1994) 3502-3507
14. Hashino E., Shero M., and Salvi R.J. Lysosomal targeting and accumulation of aminoglycoside antibiotics in sensory hair cells. Brain Res. 777 (1997) 75-85
15. Hornig H., Woolley P., and Luhrmann R. Decoding at the ribosomal A site: antibiotics, misreading and energy of aminoacyl-tRNA binding. Biochimie 69 (1987) 803-813
16. Jin Q.H., Zhao B., and Zhang X.J. Cytochrome c release and endoplasmic reticulum stress are involved in caspase-dependent apoptosis induced by G418. Cell. Mol. Life Sci. 61 (2004) 1816-1825
17. Johnson K.A., Lerner C.P., Di Lacio L.C., Laird P.W., Sharpe A.H., and Simpson E.M. Transgenic mice for the preparation of hygromycin-resistant primary embryonic fibroblast feeder layers for embryonic stem cell selections. Nucleic Acids Res. 23 (1995) 1273-1275
18. Johnston S.A., Anziano P.Q., Shark K., Sanford J.C., and Butow R.A. Mitochondrial transformation in yeast by bombardment with microprojectiles. Science 240 (1988) 1538-1541
19. King M.P., and Attardi G. Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation. Science 246 (1989) 500-503
20. Kingston R.E., Chen C.A., and Okayama H. Calcium phosphate transfection. In: Ausubel F.M., Brent R., Kingston R.E., Moore D.D., Seidman J.G., Smith J.A., and Struhl K. (Eds). Short Protocols in Molecular Biology (1987), Wiley, New York 9.5-9.8
21. Kossl M., Richardson G.P., and Russell I.J. Stereocilia bundle stiffness: effects of neomycin sulphate, A23187 and concanavalin A. Hear. Res. 44 (1990) 217-229
22. Larsson N.G., Garman J.D., Oldfors A., Barsh G.S., and Clayton D.A. A single mouse gene encodes the mitochondrial transcription factor A and a testis-specific nuclear HMG-box protein. Nat. Genet. 13 (1996) 296-302
23. Legros F., Lombes A., Frachon P., and Rojo M. Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins. Mol. Biol. Cell 13 (2002) 4343-4354
24. McKenzie M., and Trounce I. Expression of Rattus norvegicus mtDNA in Mus musculus cells results in multiple respiratory chain defects. J. Biol. Chem. 275 (2000) 31514-31519
25. Okumura K., Zhao M., Depinho R.A., Furnari F.B., and Cavenee W.K. Cellular transformation by the MSP58 oncogene is inhibited by its physical interaction with the PTEN tumor suppressor. Proc. Natl. Acad. Sci. USA 102 (2005) 2703-2706
26. Prezant T.R., Agapian J.V., Bohlman M.C., Bu X., Oztas S., Qiu W.Q., Arnos K.S., Cortopassi G.A., Jaber L., Rotter J.I., Shohat M., and Fischel-Ghodsian N. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat. Genet. 4 (1993) 289-294
27. Roychoudhury R., and Lam A. Construction of a broad-host-range kanamycin-resistant plasmid vector. Gene 24 (1983) 53-59
28. Sambrook J., Fritsch E.F., and Maniatis T. Molecular Cloning: A Laboratory Manual. second ed. (1989), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York
29. Steele D.F., Butler C.A., and Fox T.D. Expression of a recoded nuclear gene inserted into yeast mitochondrial DNA is limited by mRNA-specific translational activation. Proc. Natl. Acad. Sci. USA 93 (1996) 5253-5257
30. Tachibana M., Morioka H., Machino M., Amagai T., and Mizukoshi O. Aminoglycoside binding sites in the cochlea as revealed by neomycin-gold labelling. Histochemistry 85 (1986) 301-304
31. Wallace D.C. Mitochondrial diseases in man and mouse. Science 283 (1999) 1482-1488
32. Wallace D.C. Why do we still have a maternally inherited mitochondrial DNA? Insights from evolutionary medicine. Annu. Rev. Biochem. 76 (2007) 781-821
33. Walter F., Vicens Q., and Westhof E. Aminoglycoside-RNA interactions. Curr. Opin. Chem. Biol. 3 (1999) 694-704
34. Yi K.S., Chung J.H., Lee Y.H., Chung H.G., Kim I.J., Suh B.C., Kim E., Cocco L., Ryu S.H., and Suh P.G. Inhibition of the EGF-induced activation of phospholipase C-gamma1 by a single chain antibody fragment. Oncogene 20 (2001) 7954-7964
35. Yoon Y.G., Haug C.L., and Koob M.D. Interspecies mitochondrial fusion between mouse and human mitochondria is rapid and efficient. Mitochondrion 7 (2007) 223-229
36. Yoon Y.G., and Koob M.D. Transformation of isolated mammalian mitochondria by bacterial conjugation. Nucleic Acids Res. 33 (2005) e139
37. Zijlstra M., Li E., Sajjadi F., Subramani S., and Jaenisch R. Germ-line transmission of a disrupted β2-microglobulin gene produced by homologous recombination in embryonic stem cells. Nature 342 (1989) 435-438