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. 1981 Apr;146(1):312–320. doi: 10.1128/jb.146.1.312-320.1981

Ribonucleic acid synthesis during fruiting body formation in Myxococcus xanthus.

B A Smith, M Dworkin
PMCID: PMC217084  PMID: 6163763

Abstract

A method has been devised that allowed us, for the first time, to pulse-label M. xanthus cells with precursors for ribonucleic acid biosynthesis while they were undergoing fruiting body formation. Using this method, we examined patterns of ribonucleic acid (RNA) accumulation throughout the process of fruiting body formation. As development proceeded, the rate of RNA accumulation increased at two periods of the developmental cycle: once just before aggregation and once late in the cycle, when sporulation was essentially completed. In contrast to vegetatively growing cells, in which only stable RNA species are labeled during a 30-min pulse, the majority of radioactivity found in RNA from 30-min pulse-labeled developing cells was found in an unstable heterodisperse fraction that migrated to the 5S to 16S region of sucrose density gradients and sodium dodecyl sulfate-polyacrylamide gels. This pattern of incorporation could not be induced (i) by a shift down of vegetatively growing cells to a nutritionally poor medium, in which the generation time was increased to that of developing cells during the growth phase, or (ii) by plating of vegetative cells onto the same solid-surface environment as that of developing cells, but which surface supported vegetative growth rather than fruiting body formation. Thus, the RNA synthesis pattern observed appeared to be related to development per se rather than to nutritional depletion or growth on a solid surface alone. The radioactivity incorporated into the unstable 5S to 16S RNA fraction accumulated as the pulse length was increased from 10 to 30 min; in contrast, an analogous unstable fraction from vegetative cells decreased as pulse length was increased. This suggested that developmental 5S to 16S RNA was more stable than vegetative cell 5S to 16S RNA (presumptive messenger RNA). However, during a 45-min chase period, radioactivity in 30-min-pulse-labeled developmental 5S to 16S RNA decayed to an extent twice that of developmental RNA located in 16S and 23S regions of sucrose density gradients and was considerably less stable than the 5S, 16S, and 23S RNA species labeled during a 30-min pulse of vegetative cells.

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Selected References

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  1. Bacon K., Rosenberg E. Ribonucleic acid synthesis during morphogenesis in Myxococcus xanthus. J Bacteriol. 1967 Dec;94(6):1883–1889. doi: 10.1128/jb.94.6.1883-1889.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bolle A., Epstein R. H., Salser W., Geiduschek E. P. Transcription during bacteriophage T4 development: synthesis and relative stability of early and late RNA. J Mol Biol. 1968 Feb 14;31(3):325–348. doi: 10.1016/0022-2836(68)90413-0. [DOI] [PubMed] [Google Scholar]
  3. Cashel M. Regulation of bacterial ppGpp and pppGpp. Annu Rev Microbiol. 1975;29:301–318. doi: 10.1146/annurev.mi.29.100175.001505. [DOI] [PubMed] [Google Scholar]
  4. DWORKIN M. Nutritional requirements for vegetative growth of Myxococcus xanthus. J Bacteriol. 1962 Aug;84:250–257. doi: 10.1128/jb.84.2.250-257.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dworkin M., Sadler W. Induction of cellular morphogenesis in Myxococcus xanthus. I. General description. J Bacteriol. 1966 Apr;91(4):1516–1519. doi: 10.1128/jb.91.4.1516-1519.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Emerson C. P., Jr, Humphreys T. A simple and sensitive method for quantitative measurement of cellular RNA synthesis. Anal Biochem. 1971 Apr;40(2):254–266. doi: 10.1016/0003-2697(71)90384-8. [DOI] [PubMed] [Google Scholar]
  7. Erlich H., Gallant J. Synthesis and turnover of ribosomal ribonucleic acid in guanine-starved cells of Escherichia coli. J Biol Chem. 1975 Apr 25;250(8):3057–3061. [PubMed] [Google Scholar]
  8. Hames B. D., Ashworth J. M. The metabolism of macromolecules during the differentiation of Myxamoebae of the cellular slime mould Dictyostelium discoideum containing different amounts of glycogen. Biochem J. 1974 Aug;142(2):301–315. doi: 10.1042/bj1420301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kaiser D., Manoil C., Dworkin M. Myxobacteria: cell interactions, genetics, and development. Annu Rev Microbiol. 1979;33:595–639. doi: 10.1146/annurev.mi.33.100179.003115. [DOI] [PubMed] [Google Scholar]
  10. Kottel R. H., Bacon K., Clutter D., White D. Coats from Myxococcus xanthus: characterization and synthesis during myxospore differentiation. J Bacteriol. 1975 Oct;124(1):550–557. doi: 10.1128/jb.124.1.550-557.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Loening U. E. The fractionation of high-molecular-weight ribonucleic acid by polyacrylamide-gel electrophoresis. Biochem J. 1967 Jan;102(1):251–257. doi: 10.1042/bj1020251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Manoil C., Kaiser D. Accumulation of guanosine tetraphosphate and guanosine pentaphosphate in Myxococcus xanthus during starvation and myxospore formation. J Bacteriol. 1980 Jan;141(1):297–304. doi: 10.1128/jb.141.1.297-304.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Manoil C., Kaiser D. Guanosine pentaphosphate and guanosine tetraphosphate accumulation and induction of Myxococcus xanthus fruiting body development. J Bacteriol. 1980 Jan;141(1):305–315. doi: 10.1128/jb.141.1.305-315.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Ramsey W. S., Dworkin M. Stable messenger ribonucleic acid and germination of Myxococcus xanthus microcysts. J Bacteriol. 1970 Feb;101(2):531–540. doi: 10.1128/jb.101.2.531-540.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Smith B. A., Dworkin M. Adenylate energy charge during fruiting body formation by Myxococcus xanthus. J Bacteriol. 1980 Jun;142(3):1007–1009. doi: 10.1128/jb.142.3.1007-1009.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Stanley P. E., Williams S. G. Use of the liquid scintillation spectrometer for determining adenosine triphosphate by the luciferase enzyme. Anal Biochem. 1969 Jun;29(3):381–392. doi: 10.1016/0003-2697(69)90323-6. [DOI] [PubMed] [Google Scholar]
  17. Stanley W. M., Jr, Bock R. M. Isolation and physical properties of the ribosomal ribonucleic acid of Escherichia coli. Biochemistry. 1965 Jul;4(7):1302–1311. doi: 10.1021/bi00883a014. [DOI] [PubMed] [Google Scholar]
  18. Sudo S. Z., Dworkin M. Resistance of vegetative cells and microcysts of Myxococcus xanthus. J Bacteriol. 1969 Jun;98(3):883–887. doi: 10.1128/jb.98.3.883-887.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Watson B. F., Dworkin M. Comparative intermediary metabolism of vegetative cells and microcysts of Myxococcus xanthus. J Bacteriol. 1968 Nov;96(5):1465–1473. doi: 10.1128/jb.96.5.1465-1473.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. White D., Dworkin M., Tipper D. J. Peptidoglycan of Myxococcus xanthus: structure and relation to morphogenesis. J Bacteriol. 1968 Jun;95(6):2186–2197. doi: 10.1128/jb.95.6.2186-2197.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Wireman J. W., Dworkin M. Morphogenesis and developmental interactions in myxobacteria. Science. 1975 Aug 15;189(4202):516–523. doi: 10.1126/science.806967. [DOI] [PubMed] [Google Scholar]
  22. Wireman J. Developmental induction of Myxococcus xanthus myxospores. J Bacteriol. 1979 Oct;140(1):147–153. doi: 10.1128/jb.140.1.147-153.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]

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