Ultrastructural aspects of the self-incompatibility mechanism in Lycopersicum peruvianum Mill.

The experimental results obtained show that the tip of the incompatible pollen tube bursts open after the outer-wall has considerably expanded in the intercellular spaces of the conducting tissue and the inner-wall has disappeared and numerous particles have accumulated in the tube cytoplasm. These particles, which measure approximately 0.2 µm in diameter and give a weak reaction to the test of Thiery, differ in many respects from the vesicles normally present in compatible pollen tubes growing through the style; they appear to resemble, in some cases, the spheres which are discharged by the compatible pollen tubes after they have reached the embryo-sac. It is considered that these observations support the current belief that the tube wall is the site of action for the incompatibility proteins and suggest that self-incompatibility is not a passive process resulting from lack of growth stimulation but an active event which leads to the destruction of the incompatible pollen tubes. The degradation mechanism involved appears similar to the one which enables the compatible pollen tube to release its contents in the degenerated synergid and presents some analogies with the lytic process taking place in virus-infected cells. The general hypothesis is presented that the particles observed in the cytoplasm of self-incompatible pollen tubes consist of a mixture of incompatibility proteins and of basic constituents of the tube wall.

[1]  D. A. Larson FINE-STRUCTURAL CHANGES IN THE CYTOPLASM OF GERMINATING POLLEN. , 1965, American journal of botany.

[2]  D. B. Fisher,et al.  Cotton embryogenesis: The entrance and discharge of the pollen tube in the embryo sac , 1967, Planta.

[3]  K. K. Pandey Elements of the S -gene complex , 1964 .

[4]  K. K. Pandey Origin of Genetic Variability: Combinations of Peroxidase Isozymes determine Multiple Allelism of the S Gene , 1967, Nature.

[5]  W. G. Rosen Ultrastructure and Physiology of Pollen , 1968 .

[6]  F. W. Martin,et al.  Staining and observing pollen tubes in the style by means of fluorescence. , 1959, Stain technology.

[7]  M. Sassen FINE STRUCTURE OF PETUNIA POLLEN GRAIN AND POLLEN TUBE , 1964 .

[8]  A. G. Diboll FINE STRUCTURAL DEVELOPMENT OF THE MEGAGAMETOPHYTE OF ZEA MAYS FOLLOWING FERTILIZATION , 1968 .

[9]  J. Heslop-Harrison,et al.  Pollen-wall proteins: the fate of intine-held antigens on the stigma in compatible and incompatible pollinations of Phalaris tuberosa L. , 1971, Journal of cell science.

[10]  E. Reynolds THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY , 1963, The Journal of cell biology.

[11]  J. Heslop-Harrison,et al.  Localization of Antigens associated with the Pollen Grain Wall by Immunofluorescence , 1970, Nature.

[12]  M. L. Watson Staining of Tissue Sections for Electron Microscopy with Heavy Metals , 1958, The Journal of biophysical and biochemical cytology.

[13]  J. Thiery Mise en evidence des polysaccharides sur coupes fines en microscopie electronique , 1967 .

[14]  Y. Mäkinen,et al.  Immunological analysis of incompatibility ( S) proteins and of cross-reacting material in a self-compatible mutant of Oenothera organensis , 1962 .

[15]  D. Lewis,et al.  Immunological Reactions of Single Pollen Grains, Electrophoresis and Enzymology of Pollen Protein Exudates , 1967 .

[16]  M. Nasrallah,et al.  Self-incompatibility proteins in plants: detection, genetics, and possible mode of action1 , 1970, Heredity.

[17]  C. Rick,et al.  Self-incompatibility in species ofLycopersiconSect.Eriopersiconand hybrids withL. esculentum , 1954 .