Skip to main content
Log in

Changes in protein and amino acid content during anther development in fertile and cytoplasmic male sterile Petunia

  • Published:
Theoretical and Applied Genetics Aims and scope Submit manuscript

Summary

Development of anthers in cytoplasmic male sterile (CMS) Petunia diverges from the normal sequence of events early in meiosis. Quantitative and qualitative changes in morphology, proteins and free amino acid contents correlate with this divergence. In anthers of the fertile line (5719), total protein content increases, and SDS-PAGE protein patterns change as the anthers mature. Enhanced levels of three polypeptides with molecular weights of 64,000, 63,000 and 45,000 daltons characterize premeiosis in fertile anthers. Protein levels and patterns from anthers of the CMS line (5707) show little alteration during anther development. Protein synthesis seems to be at least partially blocked in the CMS microspore. The 63,000 and 45,000 dalton proteins are not present, and the absence of any unique protein(s) in the CMS line argues against a virus as the causal agent of CMS in Petunia. Analysis of free amino acids from anthers of the fertile line shows levels of proline and pipecolic acid 2–3 and 10–20 fold higher, respectively, than in the CMS line. The amino acids incorporated into proteins show no such differences; analysis of protein hydrolysates shows similar levels of each amino acid in both fertile and CMS lines at every developmental stage examined.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Dungey NO, Davis DD (1982) Protein turnover in isolated barley leaf segments and the effect of stress. J Exp Bot 33:12–20

    Google Scholar 

  • Edwardson JR (1970) Cytoplasmic male sterility. Bot Rev 36: 341–420

    Google Scholar 

  • Edwardson JR, Corbett MK (1961) Asexual transmission of cytoplasmic male sterility. Proc Natl Acad Sci USA 47: 390–396

    Google Scholar 

  • Frankel R, Izhar S, Nitsan J (1969) Timing of callase activity and cytoplasmic male sterility in Petunia. Biochem Genet 3:451–455

    Google Scholar 

  • Gerstel GU (1980) Cytoplasmic male sterility in Nicotiana (a review). NC Agric Res Serv Tech Bull 263:1–31

    Google Scholar 

  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680–685

    Google Scholar 

  • Laser KD, Lersten NR (1972) Anatomy and cytology of microsporogenesis in cytoplasmic male sterile angiosperms. Bot Rev 38:425–454

    Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275

    Google Scholar 

  • McLellan T, Ames GFL, Nikaido K (1983) Genetic variation in proteins: comparison of one-dimensional and twodimensional gel electrophoresis. Genetics 104:381–390

    Google Scholar 

  • Nakashima H (1978) Physiological and morphological studies on the cytoplasmic male sterility of some crops. J Fac Agric Hokkaido Univ 59:17–58

    Google Scholar 

  • Palfi G, Pinter L, Palfi Z (1981) The proline content and fertility of the pollen of inbred maize lines. Acta Bot Acad Sci Hung 27:179–187

    Google Scholar 

  • Pearson OH (1981) Nature and mechanisms of cytoplasmic male sterility in plants (a review). Hortic Sci 16:482–487

    Google Scholar 

  • Rhodes D, Myers AC, Jamieson G (1981) Gas chromatography-mass spectrometry of N-heptafluorobutyl esters of amino acids in the analysis of the kinetics of (15N)Hx + assimilation in Lemna minor L. Plant Physiol 68:1197–1205

    Google Scholar 

  • Stanley RG, Linskens HF (1974) Pollen biology, biochemistry, and management. Springer, Berlin Heidelberg New York, pp 154–163

    Google Scholar 

  • Stewart GR, Lahrer F (1980) Accumulation of amino acids and related compounds in relation to environmental stress. In: Miflin BJ (ed) The biochemistry of plants, amino acids and their derivations. Academic Press, New York, pp 609–635

    Google Scholar 

  • Tupy J (1963) Free amino acids in apple pollen from the point of view of its fertility. Biol Plant (Praha) 5:154–160

    Google Scholar 

  • Wu FS, Lucas-Lenard JM (1980) Inhibition of ribonucleic acid accumulation in mouse L cells infected with vesicular stomatitis virus requires viral ribonucleic acid transcription. Biochemistry 19:804–810

    Google Scholar 

  • Wu FS, Wang M-Y (1984) Extraction of proteins for SDS polyacrylamide gel electrophoresis from protease rich plant tissues. Anal Biochem 139:100–103

    Google Scholar 

  • Zhang HQ, Croes AF (1983) Proline metabolism in pollen: degradation of proline during germination and early tube growth. Planta 159:46–49

    Google Scholar 

  • Zhang HQ, Croes AF, Linskens HF (1982) Protein synthesis in germinating pollen of Petunia: role of proline. Planta 154:199–203

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by H. F. Linskens

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wu, F.S., Murry, L.E. Changes in protein and amino acid content during anther development in fertile and cytoplasmic male sterile Petunia . Theoret. Appl. Genetics 71, 68–73 (1985). https://doi.org/10.1007/BF00278256

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00278256

Key words

Navigation