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Phytohormone control of translatable RNA populations in sexual organogenesis of the dioecious plant Mercurialis annua L. (2n = 16)

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Abstract

A cell-free translation system was programmed with total, poly(A), non poly(A) and polysomal RNAs from male and female flowers of this plant with separated sexes. The peptide patterns obtained reflected differences in corresponding translatable RNAs. In total RNA products, three peptides were specific for males, two for females. One of the two male-specific polypeptides of high molecular weight was obtained from poly(A) RNAs and a female-specific one from non poly(A) RNAs. Differences between peptides common to both sexes reflected different concentrations of corresponding messengers. Similar results were obtained with polysomal RNAs. The male-specific RNAs were depending on high endogenous auxin concentrations while the female on active cytokinins. Cytokinin feminization of males induced the female-specific RNAs showing cytokinin action at pretranslational stages. Phytohormone roles are discussed.

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References

  1. Aspart L, Cooke R, Delseny M: Stability of polyadenylic and polyadenylated ribonucleic acids in radish (Raphanus sativus) seedling. Biochem Biophys Acta 564: 43–54, 1979.

    Google Scholar 

  2. Baulcombe DC, Key JL: Polyadenylated RNA sequences which are reduced in concentration following auxin treatment of soybean hypocotyls. J Biol Chem 255: 8907–8913, 1980.

    Google Scholar 

  3. Bazin M, Chabin A, Durand R: Comparison between four isoaccepting transfer ribonucleic acids and corresponding synthetases in male and female flowers of the dioecious species, Mercurialis annua L. Dev Biol 44: 288–297, 1975.

    Google Scholar 

  4. Bostock CJ, Prescott DM, Lauth M: Lability of 26S ribosomal RNA in Tetrahymena pyriformis. Exp Cell Res 66: 260–262, 1971.

    Google Scholar 

  5. Bowden-Bonnets L, Lord JM: Isolation and cell-free translation of total messenger RNA from germinating castor bean endosperm. Plant Physiol 63: 769–773, 1979.

    Google Scholar 

  6. Champault A: Detection et dosage par chromatographie en phase gazeuse de l'acide idolyl-acétique extrait de deux souches tissulaires de l'espèce Mercurialis annua L. (2n=16). C.R. Acad. Sc. Paris, série D280: 591–594, 1975.

    Google Scholar 

  7. Champault A, Chung S, Guerin B, Kahlem G, Lhermitte A, Teller G, Durand R, Durand B: Towards an understanding of the mechanism of cytokinin activity in Mercurialis annua L. sex differentiation. In: Guern J, C Peaud-Lenoël (eds) Metabolism and molecular activities of cytokinins. Springer Verlag Heidelberg, 1981, pp 129–139.

    Google Scholar 

  8. Chantrenne H, Burny A, Marbaix G: The search for the messenger RNA of hemoglobin. Nucleic Acids Res. 7: 173–194, 1976.

    Google Scholar 

  9. Cuming AC, Kennedy TD, Lane BG: Wheat embryo ribonucleates XIV. Mass isolation of mRNA from wheat germ and comparison of its translational capacity with that of mRNA from imbibing wheat embryos. Can J Biochem 57: 1170–1175, 1979.

    Google Scholar 

  10. Dauphin-Guérin B, Teller G, Durand B: Different endogenous cytokinins between male and female Mercurialis annua L. Planta 148: 124–129, 1980.

    Google Scholar 

  11. Dure LIII, Greenway SC, Galau GA: Developmental biochemistry of cottonseed embryogenesis and germination: changing messenger ribonucleic acid populations as shown by in vitro and in vivo protein synthesis. Biochemistry 20: 4162–4168, 1981.

    Google Scholar 

  12. Elliott RM, Davison AN, Lim L: Developmental changes in the protein and ribonucleic acid components of rat brain messenger ribonucleic acid-protein particules isolated from free polysomes by oligo-(dT)-cellulose chromatography. Biochem J 190: 215–223, 1980.

    Google Scholar 

  13. Galau GA, Dure LIII: Developmental biochemistry of cottonseed embryogenesis and germination: changing messenger ribonucleic acid populations as shown by reciprocal heterologous complementary deoxyribonucleic acid-messenger ribonucleic acid hybridization. Biochemistry 20: 4169–4178, 1981.

    Google Scholar 

  14. Gilham PT: The synthesis of polynucleotide-celluloses and their use in the fractionation of polynucleotides. J Chem Am Soc 83: 4982–4985, 1964.

    Google Scholar 

  15. Goldberg RB, Hoschek G, Tam SH, Ditta GS, Breidenbach RW: Abundance, diversity and regulation of mRNA sequence sets in soybean embryogenesis. Dev Biol 83: 201–217, 1981.

    Google Scholar 

  16. Goldstein ES: Translated and sequestral intranslated message sequences in Drosophila oocytes and embryos. Dev Biol 63: 59–66, 1978.

    Google Scholar 

  17. Grierson D, Covey S: Changes in the amount of ribosomal RNA and Poly-(A) containing RNA during leaf development. Planta 127: 77–86, 1976.

    Google Scholar 

  18. Grierson D, Hemleben V: Ribonucleic acid from the higher plant Matthiola incana. Molecular weight measurements and DNA-RNA hybridization studies. Biochem Biophys Acta 475: 424–436, 1977.

    Google Scholar 

  19. Guilfoyle TJ, Lin CY, Chen YM, Nagao RI, Key JL: Enhancement of soybean RNA polymerase I by auxin. Proc Natl Acad Sci USA 72: 69–72, 1975.

    Google Scholar 

  20. Hagenbuchle O, Schibler U, Wiler T: Intermolecular renaturation of hairpin loops leads to stable and specific aggregates of 28 S rRNA and precursors rRNAs from Xenopus laevis. Eur J Biochem 60: 73–82, 1975.

    Google Scholar 

  21. Jackson AO, Larkins BA: Influence of ionic strengh, pH, and chelation of divalent metals on isolation of polyribosomes from tobacco leaves Plant Physiol 57: 5–10, 1976.

    Google Scholar 

  22. Kahlem G, Champault A, Louis JP, Bazin M, Chabin A, Delaigue M, Dauphin B, Durand R, Durand B: Détermination génétique et régulation hormonale de la différenciation sexuelle chez Mercurialis annua L. Physiol Vég 13: 763–779, 1975.

    Google Scholar 

  23. Kahlem G: Isolation and localization by histoimmunology of isoperoxidases specific for male flowers of the dioecious species Mercurialis annua L. Dev Biol 50: 58–67, 1976.

    Google Scholar 

  24. Kamalay JC, Goldberg RB: Regulation of structural gene expression in tobacco. Cell 19: 935–946, 1980.

    Google Scholar 

  25. Key JL, Silflow C: The occurence and distribution of poly(A) ribonucleic acid in Soybean. Plant Physiol 56: 364–369, 1975.

    Google Scholar 

  26. Louis JP, Durand B: Studies with the dioecious Angiosperm Mercurialis annua L. (2n=16). Correlation between genic and cytoplasmic male sterility, sex segregation and feminizing hormones (cytokinins). Mol gen Genet 165: 309–322, 1978.

    Google Scholar 

  27. Lovett JA, Goldstein ES: The cytoplasmic distribution and characterization of Poly(A)-RNA in oocytes and embryos of Drosophila. Dev Biol 61: 70–78, 1977.

    Google Scholar 

  28. Marcus A: Tobacco mosaïc virus ribonucleic acid-dependent aminoacid incorporation in a wheat embryo system in vitro. Analysis of the rate-limiting reactions. J Biol Chem 245: 955–961, 1970.

    Google Scholar 

  29. Melera PW, Davide JP, Hession C: Identification of mRNA in the slime mold Physarum polycephalum. Eur J Biochem 96: 373–378, 1979.

    Google Scholar 

  30. Myhal ML, Hufnagel LA: Poly(A)-RNA from Tetrahymena. Stimulation of protein synthesis in vitro. J. Protozool. 26, 672–675, 1979.

    Google Scholar 

  31. Newbury HJ, Possingham JV: Factors affecting the extraction of intact ribonucleic acid from plant tissues containing interfering phenolic compounds. Plant Physiol 60: 543–547, 1977.

    Google Scholar 

  32. O'Farrell PH: High resolution two-dimensional electrophoresis of proteins. J Biol Chem 250: 4007–4021, 1975.

    Google Scholar 

  33. Pelham HRB, Jackson RJ: An efficient mRNA-dependent translation system from reticulocyte lysates. Eur J Biochem 67: 247–256, 1976.

    Google Scholar 

  34. Pinder JC, Staynov DZ, Gratzer WB: Properties of RNA in formamide. Biochemistry 13: 5367–5373, 1974.

    Google Scholar 

  35. Rosenthal ET, Hunt T, Ruderman JV: Selective translation of mRNA controls of the pattern of protein synthesis during early development of the surf clam, Spinosula solidissima. Cell 20: 487–494, 1980.

    Google Scholar 

  36. Sagher D, Edelman M, Jakob LM: Poly(A) associated RNA in plants. Biochem Biophys Acta 349: 32–38, 1974.

    Google Scholar 

  37. Tessier L, Esnault R: Isolation and characterization of polysomes and polyadenylated polysomal RNA from Vicia faba meristematic root cells. Mol Cell Biochem 29: 173–182, 1980.

    Google Scholar 

  38. Ts'o POP, Helmkamp GK, Sander C: Secondary structure of nucleic acids in organic solvents. II. Optical properties of nucleotides and nucleic acids. Biochem Biophys Acta 55: 584–593, 1962.

    Google Scholar 

  39. Trapy G, Esnault R: Characteristics of Vicia faba meristematic root cells polyadenylated RNAs purified by thermal elution from Poly(U) sepharose. Acides nucléiques et synthèse des protéines chez les végétaux. Coll Int CNRS 261: 381–385, 1977.

    Google Scholar 

  40. Walker JC, Key JL: Isolation of cloned cDNAs to auxin-responsive poly(A)+ RNAs of elongating soybean hypocotyl. Proc Natl Acad Sci USA 79: 7185–7189, 1982.

    Google Scholar 

  41. Wong LJC, Marzluf CA: Sequence complexity and abundance classes of nuclear and polysomal polyadenylated RNA in Neurospora crassa. Biochem Biophys Acta 607: 122–135, 1980.

    Google Scholar 

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Delaigue, M., Poulain, T. & Durand, B. Phytohormone control of translatable RNA populations in sexual organogenesis of the dioecious plant Mercurialis annua L. (2n = 16). Plant Mol Biol 3, 419–429 (1984). https://doi.org/10.1007/BF00033390

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  • DOI: https://doi.org/10.1007/BF00033390

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