α-Tubulin and F-actin distribution during microsporogenesis in a 2n pollen producer of Solanum

Spatial and temporal changes in configurations of microtubules (MTs) and microfilaments (MFs) were determined during microsporogenesis, using α-tubulin immunolocalization and rhodamine-phalloidin staining of F- actin, in a 2n pollen producer of Solanum, to assess the anomalies in meiotic spindles and cytokinesis and their relationships to 2n pollen formation. In Solanum, MTs and MFs generally showed patterns of localization similar to those described in other dicotyledons with simultaneous cytokinesis. However, deviations in spatial configurations of both MTs and MFs that are related to 2n pollen were observed in meiosis II and in cytokinesis. MTs and MFs localized in spindles in parallel orientation at meiosis II. In contrast, in the majority of normal meiocytes, the two spindles were seen to be perpendicular to each other. The parallel spindles altered the position of the postmeiotic nuclei, causing a uniplanar instead of a tetrahedral arrangement. Subsequently, the formation of regular radial MT systems was suppressed and only two MT arrays, which lay parallel on one plane, formed between the nuclei at the end of meiosis. A single cell plate formed across the two MT arrays, giving rise to a dyad containing 2n microspores.

[1]  S. J. Peloquin,et al.  2n pollen in eleven 2x, 2EBN wild species and their haploid x wild species hybrids , 1988, Potato Research.

[2]  A. Dinis,et al.  The F-actin distribution during microsporogenesis in Magnolia soulangeana Soul. (Magnoliaceae) , 1993, Sexual Plant Reproduction.

[3]  A. Lammeren,et al.  Organization of the actin cytoskeleton during pollen development inGasteria verrucosa (Mill.) H. Duval visualized with rhodamine-phalloidin , 1989, Planta.

[4]  T. Cardi,et al.  Early tapetal degeneration and meiotic defects are involved in the male sterility of Solanum commersonii (+) S. tuberosum somatic hybrids , 1997, Theoretical and Applied Genetics.

[5]  S. J. Peloquin,et al.  Cytological basis of 2n pollen formation in a wide range of 2x, 4x, and 6x taxa from tuber-bearing Solanum species. , 1993, Genome.

[6]  C. Staiger,et al.  Cytoskeletal analysis of maize meiotic mutants , 1993 .

[7]  G. Cai,et al.  The Microtubular Cytoskeleton during Pollen Development and Pollen Tube Growth in Nicotiana tabacum , 1992 .

[8]  C. Staiger,et al.  Microfilament Distribution in Maize Meiotic Mutants Correlates with Microtubule Organization. , 1991, The Plant cell.

[9]  C. Staiger,et al.  Microtubule distribution in dv, a maize meiotic mutant defective in the prophase to metaphase transition. , 1990, Developmental biology.

[10]  J. Traas,et al.  The Organization of the Cytoskeleton During Meiosis in Eggplant (Solanum Melongena (L.)): Microtubules and F-Actin are Both Necessary for Coordinated Meiotic Division , 1989 .

[11]  S. J. Peloquin,et al.  Potato breeding with haploids and 2n gametes , 1989 .

[12]  C. Lloyd,et al.  THE PLANT CYTOSKELETON: The Impact of Fluorescence Microscopy , 1987 .

[13]  J. Hermsen The potential of meiotic polyploidization in breeding allogamous crops , 1984 .

[14]  R. Veilleux,et al.  2n GAMETES IN DIPLOID SOLANUM: FREQUENCY AND TYPES OF SPINDLE ABNORMALITIES , 1982 .

[15]  S. J. Peloquin,et al.  The inheritance of three mechanisms of diplandroid (2n pollen) formation in diploid potatoes , 1975, Heredity.

[16]  S. J. Peloquin,et al.  THREE MECHANISMS OF 2n POLLEN FORMATION IN DIPLOID POTATOES , 1975 .