A B S T R A C TInterphase, preprophase, and prophase nuclei of meristematic cells of AUium ¢epa, Vide faba, and Raphanus sativus are characterized by the presence of spherical bodies approximately 1 /~ in diameter. These structures are Feulgen-negative but stain metachromatlcaUy with azure B, as the nucleolus, following fixation with glutaraldehyde. At the ultrastructural level, they consist predominantly of fibrils estimated to be between 70 and 100 A in diameter which greatly resemble those found within certain zones of the nucleolus in these plant species. Moreover, in Allium ¢epa, these spherules often exhibit dense particles which are also found within the fibrillar zones of the nucleolus in this species. The observations that the bodies in question are frequently located at the surface of the nucleolus and moreover show cytochemical and ultrastructural similarities with this organelle suggest that they may originate from the nucleolus. However, the common association of the spherules with chromosome strands may indicate instead that these bodies represent extranucleolar ribonucleoprotein materials synthesized by specific chromosomal loci.
I N T R O D U C T I O NIn the course of an earlier electron microscope study (1) of nuclear structures in meristematic cells of Allium cepa and Vicia faba, spherical bodies, approximately 2 /z in diameter, were observed at interphase. These structures were lighter than either the chromosomes or the nucleolus under electron microscopy, but stained metachromatically with azure B, as the nucleolus, following fixation with formalin. Since then, nuclear bodies of a similar appearance have been noted in Tetrahymena pyriformis (2,3), in kidney (4, 5), and thymus (6).The purpose of the present paper is to describe in more detail the distribution of these bodies during interphase, preprophase, and prophase and to report certain characteristics which they share with the nucleolus.
M A T E R I A L A N D M E T H O D SRoots of Allium cepa grown in distilled water and of Vicia faba and Raphanus sativus L. grown in damp vermiculite were used for the present study. Portions 0.5 to 1 mm in length were excised from the root tips and fixed in the following solutions: (a) 1 per cent osmium tetroxide in distilled water (7), (b) 1 per cent osmium tetroxide buffered with Veronal (8) or phosphate (9) to a pH of 7.3, (c) 4 per cent formaldehyde or glutaraldehyde. Other roots were fixed in one of these aldehydes and postfixed in 1 per cent osmium tetroxide (10). Following dehydration in alcohol the specimens were embedded in Epon 812. Sections 0.25 to 0.75 D thick were stained with Feulgen and methylene blue (11); ultrathin sections were stained with solutions of heavy metals (12, 13). Electron micrographs were obtained with a Siemens on