Abstract
Red cell-mediated microinjection has been used to study tRNA turnover in SV3T3 mouse cells and TC7 cells, an African green monkey kidney line. The turnover of endogenous tRNA, measured by labeling with 3H-methionine, was first-order with half-lives of approximately one day in SV3T3 and two days in TC7 cells. 32PtRNA isolated from E. coli or TC7 cells turned over at the same rate as endogenous tRNA when injected into either SV3T3 or TC7 cells. This demonstrates that cellular processes, not properties inherent to tRNAs, are responsible for the difference in tRNA turnover observed between SV3T3 and TC7 cells. These results further indicate that the mechanism of tRNA turnover in mammaliam cells does not distinguish prokaryotic from eukaryotic tRNAs. In contrast to unmodified tRNA, glyoxalated tRNA was rapidly degraded upon injection. Thus altered tRNA's, like altered proteins, are turned over more rapidly in animal cells.
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Selected References
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- Aboud M., Pastan I. Activation of transcription by guanosine 5'-diphosphate,3'-diphosphate, transfer ribonucleic acid, and novel protein from Escherichia coli. J Biol Chem. 1975 Mar 25;250(6):2189–2195. [PubMed] [Google Scholar]
- Agris P. F. Alterations of transfer RNA during erythroid differentiation of murine virus-induced leukemia cells. Arch Biochem Biophys. 1975 Sep;170(1):114–123. doi: 10.1016/0003-9861(75)90102-2. [DOI] [PubMed] [Google Scholar]
- Allende C. C., Allende J. E., Firtel R. A. The degradation of ribonucleic acids injected into Xenopus laevis oocytes. Cell. 1974 Jul;2(3):189–196. doi: 10.1016/0092-8674(74)90093-2. [DOI] [PubMed] [Google Scholar]
- Arfin S. M., Simpson D. R., Chiang C. S., Andrulis I. L., Hatfield G. W. A role for asparaginyl-tRNA in the regulation of asparagine synthetase in a mammalian cell line. Proc Natl Acad Sci U S A. 1977 Jun;74(6):2367–2369. doi: 10.1073/pnas.74.6.2367. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bender W., Davidson N. Mapping of poly(A) sequences in the electron microscope reveals unusual structure of type C oncornavirus RNA molecules. Cell. 1976 Apr;7(4):595–607. doi: 10.1016/0092-8674(76)90210-5. [DOI] [PubMed] [Google Scholar]
- Blobel G., Potter V. R. Distribution of radioactivity between the acid-soluble pool and the pools of RNA in the nuclear, nonsedimethable and ribosome fractions of rat liver after a single injection of lebaled orotic acid. Biochim Biophys Acta. 1968 Aug 23;166(1):48–57. doi: 10.1016/0005-2787(68)90489-9. [DOI] [PubMed] [Google Scholar]
- Borek E., Baliga B. S., Gehrke C. W., Kuo C. W., Belman S., Troll W., Waalkes T. P. High turnover rate of transfer RNA in tumor tissue. Cancer Res. 1977 Sep;37(9):3362–3366. [PubMed] [Google Scholar]
- Croce C. M., Koprowski H. Enucleation of cells made simple and rescue of SV40 by enucleated cells made even simpler. Virology. 1973 Jan;51(1):227–229. doi: 10.1016/0042-6822(73)90382-6. [DOI] [PubMed] [Google Scholar]
- Delaney P., Siddiqui M. A. Changes in the in vivo levels of charged transfer RNA species during development of the posterior silkgland of Bombyx mori. Dev Biol. 1975 May;44(1):54–62. doi: 10.1016/0012-1606(75)90376-0. [DOI] [PubMed] [Google Scholar]
- Erdos T., Bessada R. The turnover of ribosomal RNA and soluble RNA in the rabbit uterus. Biochim Biophys Acta. 1966 Dec 21;129(3):628–631. doi: 10.1016/0005-2787(66)90080-3. [DOI] [PubMed] [Google Scholar]
- Fournier A., Chavancy G., Garel J. P. Turnover of transfer RNA species during development of the posterior silkgland of Bombyx mori L. Biochem Biophys Res Commun. 1976 Oct 4;72(3):1187–1194. doi: 10.1016/s0006-291x(76)80256-2. [DOI] [PubMed] [Google Scholar]
- Furusawa M., Nishimura T., Yamaizumi M., Okada Y. Injection of foreign substances into single cells by cell fusion. Nature. 1974 May 31;249(456):449–450. doi: 10.1038/249449a0. [DOI] [PubMed] [Google Scholar]
- Ghosh R. K., Deutscher M. P. Identification of an Escherichia coli nuclease acting on structurally altered transfer RNA molecules. J Biol Chem. 1978 Feb 25;253(4):997–1000. [PubMed] [Google Scholar]
- Goldberg A. L., Dice J. F. Intracellular protein degradation in mammalian and bacterial cells. Annu Rev Biochem. 1974;43(0):835–869. doi: 10.1146/annurev.bi.43.070174.004155. [DOI] [PubMed] [Google Scholar]
- Hanoune Jacques, Agarwal M. K. Studies on the half life time of rat liver transfer RNA species. FEBS Lett. 1970 Nov 18;11(2):78–80. doi: 10.1016/0014-5793(70)80496-3. [DOI] [PubMed] [Google Scholar]
- Hendil K. B. Intracellular protein degradation in growing, in density-inhibited, and in serum-restricted fibroblast cultures. J Cell Physiol. 1977 Sep;92(3):353–364. doi: 10.1002/jcp.1040920304. [DOI] [PubMed] [Google Scholar]
- Holmes W. M., Goldman E., Miner T. A., Hatfield G. W. Differential utilization of leucyl-tRNAs by Escherichia coli. Proc Natl Acad Sci U S A. 1977 Apr;74(4):1393–1397. doi: 10.1073/pnas.74.4.1393. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson L. F., Levis R., Abelson H. T., Green H., Penman S. Changes in RNA in relation to growth of the fibroblast. IV. Alterations in theproduction and processing of mRNA and rRNA in resting and growing cells. J Cell Biol. 1976 Dec;71(3):933–938. doi: 10.1083/jcb.71.3.933. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kaji H. Amino-terminal arginylation of chromosomal proteins by arginyl-tRNA. Biochemistry. 1976 Nov 16;15(23):5121–5125. doi: 10.1021/bi00668a027. [DOI] [PubMed] [Google Scholar]
- Kaltoft K., Zeuthen J., Engbaek F., Piper P. W., Celis J. E. Transfer of tRNAs to somatic cells mediated by Sendai-virus-induced fusion. Proc Natl Acad Sci U S A. 1976 Aug;73(8):2793–2797. doi: 10.1073/pnas.73.8.2793. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Koprowski H., Jensen F. C., Steplewski Z. Activation of production of infectious tumor virus SV40 in heterokaryon cultures. Proc Natl Acad Sci U S A. 1967 Jul;58(1):127–133. doi: 10.1073/pnas.58.1.127. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kuchino Y., Borek E. Tumour-specific phenylalanine tRNA contains two supernumerary methylated bases. Nature. 1978 Jan 12;271(5641):126–129. doi: 10.1038/271126a0. [DOI] [PubMed] [Google Scholar]
- Lengyel J. A., Penman S. Differential stability of cytoplasmic RNA in a Drosophila cell line. Dev Biol. 1977 Jun;57(2):243–253. doi: 10.1016/0012-1606(77)90212-3. [DOI] [PubMed] [Google Scholar]
- Loyter A., Zakai N., Kulka R. G. "Ultramicroinjection" of macromolecules or small particles into animal cells. A new technique based on virus-induced cell fusion. J Cell Biol. 1975 Aug;66(2):292–304. doi: 10.1083/jcb.66.2.292. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nomura Y. Biological evidence for possibility of the intracellular mechanism scavenging 'deformed tRNA molecules'. FEBS Lett. 1974 Sep 1;45(1):223–227. doi: 10.1016/0014-5793(74)80849-5. [DOI] [PubMed] [Google Scholar]
- Ortwerth B. J., Liu L. P. Correlation between a specific isoaccepting lysyl transfer ribonucleic acid and cell division in mammalian tissues. Biochemistry. 1973 Sep 25;12(20):3978–3984. doi: 10.1021/bi00744a030. [DOI] [PubMed] [Google Scholar]
- PATTERSON M. S., GREENE R. C. MEASUREMENT OF LOW ENERGY BETA-EMITTERS IN AQUEOUS SOLUTION BY LIQUID SCINTILLATION COUNTING OF EMULSIONS. Anal Chem. 1965 Jun;37:854–857. doi: 10.1021/ac60226a017. [DOI] [PubMed] [Google Scholar]
- Poste G., Schaeffer B., Reeve P., Alexander D. J. Rescue of simian virus 40 (SV 40) from SV40-transformed cells by fusion with anucleate monkey cells and variation in the yield of virus rescued by fusion with replicating or nonreplicating monkey cells. Virology. 1974 Jul;60(1):85–95. doi: 10.1016/0042-6822(74)90368-7. [DOI] [PubMed] [Google Scholar]
- Schlegel R. A., Rechsteiner M. C. Microinjection of thymidine kinase and bovine serum albumin into mammalian cells by fusion with red blood cells. Cell. 1975 Aug;5(4):371–379. doi: 10.1016/0092-8674(75)90056-2. [DOI] [PubMed] [Google Scholar]
- Sharma O. K., Beezley D. N., Roberts W. K. Limitation of reticulocyte transfer RNA in the translation of heterologous messenger RNAs. Biochemistry. 1976 Sep 21;15(19):4313–4318. doi: 10.1021/bi00664a027. [DOI] [PubMed] [Google Scholar]
- Smith D. W. Reticulocyte transfer RNA and hemoglobin synthesis. Science. 1975 Nov 7;190(4214):529–535. doi: 10.1126/science.1103288. [DOI] [PubMed] [Google Scholar]
- Sprague K. U., Hagenbüchle O., Zuniga M. C. The nucleotide sequence of two silk gland alanine tRNAs: implications for fibroin synthesis and for initiator tRNA structure. Cell. 1977 Jul;11(3):561–570. doi: 10.1016/0092-8674(77)90074-5. [DOI] [PubMed] [Google Scholar]
- Takemoto K. K., Kirschstein R. L., Habel K. Mutants of simian virus 40 differing in plaque size, oncogenicity, and heat sensitivity. J Bacteriol. 1966 Oct;92(4):990–994. doi: 10.1128/jb.92.4.990-994.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waters L. C., Mullin B. C. Transfer RNA into RNA tumor viruses. Prog Nucleic Acid Res Mol Biol. 1977;20:131–160. doi: 10.1016/s0079-6603(08)60471-7. [DOI] [PubMed] [Google Scholar]
- Watkins J. F., Dulbecco R. Production of SV40 virus in heterokaryons of transformed and susceptible cells. Proc Natl Acad Sci U S A. 1967 Oct;58(4):1396–1403. doi: 10.1073/pnas.58.4.1396. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weinberg R. A., Penman S. Small molecular weight monodisperse nuclear RNA. J Mol Biol. 1968 Dec;38(3):289–304. doi: 10.1016/0022-2836(68)90387-2. [DOI] [PubMed] [Google Scholar]
- Zilberstein A., Dudock B., Berissi H., Revel M. Control of messenger RNA translation by minor species of leucyl-transfer RNA in extracts from interferon-treated L cells. J Mol Biol. 1976 Nov;108(1):43–54. doi: 10.1016/s0022-2836(76)80093-9. [DOI] [PubMed] [Google Scholar]
