Development of surface pattern during division in Paramecium. II. Defective spatial control in the mutant kin241

• Published in: Development (Cambridge) Vol. 115; no. 1; pp. 319 - 335
• Main Authors: JERKA-DZIADOSZ, M, GARREAU DE LOUBRESSE, N, BEISSON, J
• Format: Journal Article
• Language: English
• Published: Cambridge The Company of Biologists Limited 01.05.1992; Company of Biologists
• Subjects: Animals; Biochemistry. Physiology. Immunology. Molecular biology; Biological and medical sciences; Cell Division - genetics; Fluorescent Antibody Technique; Fundamental and applied biological sciences. Psychology; Interphase; Invertebrates; Microscopy, Electron; Morphogenesis - genetics; Mutation - physiology; Paramecium - genetics; Paramecium - ultrastructure; Protozoa; Morphogenesis; Protozoa; Paramecium; Cell division; Ciliata; Mutation; Cortex protozoa
• ISSN: 0950-1991; 1477-9129
• DOI: 10.1242/dev.115.1.319

kin241 is a monogenic nuclear recessive mutation producing highly pleiotropic effects on cell size and shape, generation time, thermosensitivity, nuclear reorganization and cortical organization. We have analyzed the nature of the cortical disorders and their development during division, using various specific antibodies labelling either one of the cortical cytoskeleton components, as was previously done for analysis of cortical pattern formation in the wild type. Several abnormalities in basal body properties were consistently observed, although with a variable frequency: extra microtubules in either the triplets or in the lumen; nucleation of a second kinetodesmal fiber; abnormal orientation of the newly formed basal body with respect to the mother one. The latter effect seems to account for the major observed cortical disorders (reversal, intercalation of supplementary ciliary rows). The second major effect of the mutation concerns the spatiotemporal map of cortical reorganization during division. Excess basal body proliferation occurs and is correlated with modified boundaries of some of the cortical domains identified in the wild type on the basis of their basal body duplication pattern. This is the first mutant described in a ciliate in which both the structure and duplication of basal bodies and the body plan are affected. The data support the conclusion that the mutation does not alter the nature of the morphogenetic signal(s) which pervade the dividing cell, nor the competence of cytoskeletal structures to respond to signalling, but affects the local interpretation of the signals.