Document Detail


Looking at Drosophila mitotic chromosomes.
MedLine Citation:
PMID:  7707964     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The repertoire of cytological procedures described in the present paper permits full analysis of brain neuroblast chromosomes. Moreover, if brains are cultured for 13 hr in the presence of 5-bromo-2'-deoxy-uridine, our fixation and Hoechst staining protocols allow visualization of sister chromatid differentiation and the scoring of sister chromatid exchanges (Gatti et al., 1979). Finally, we note that our cytological procedures can be successfully employed for preparation and staining of gonial cells of both sexes and male meiotic chromosomes (Ripoll et al., 1985; our unpublished results). Good chromosome preparations of female meiosis are obtained with the procedure described by Davring and Sunner (1977, 1979), Nokkala and Puro (1976), and Puro and Nokkala (1977). In this chapter, we have focused on the organization and behavior of Drosophila mitotic chromosomes, describing a repertoire of cytological techniques for neuroblast chromosome preparations. We have not considered the numerous excellent cytological procedures for embryonic chromosome preparations (for an example, see Foe and Alberts, 1985; Foe, 1989), because these chromosomes are usually less clearly defined than those of larval neuroblasts. In addition, we have not included the whole-mount and squashing techniques that allow chromosome visualization and spindle immunostaining of neuroblast cells (Axton et al., 1990; Gonzalez et al., 1990), male meiotic cells (Casal et al.. 1990; Cenci et al., 1994), and female meiotic cells (Theurkauf and Hawley. 1992), because the fixation methods used in these procedures alter chromosome morphology. Fixation methods for antibody staining result in poorly defined chromosomes, whereas the methanol/acetic acid fixation techniques, such as those described here, preserve very well chromosome morphology but remove a substantial fraction of chromosomal proteins. Thus, one of the major technical breakthroughs in Drosophila mitotic cytology will be the development of fixation procedures that maximize chromosomal quality with minimal removal of proteins. This will be particularly useful for precise immunolocalization of heterochromatic proteins, including those associated with the centromere.
Authors:
M Gatti; S Bonaccorsi; S Pimpinelli
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review    
Journal Detail:
Title:  Methods in cell biology     Volume:  44     ISSN:  0091-679X     ISO Abbreviation:  Methods Cell Biol.     Publication Date:  1994  
Date Detail:
Created Date:  1995-05-11     Completed Date:  1995-05-11     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0373334     Medline TA:  Methods Cell Biol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  371-91     Citation Subset:  IM    
Affiliation:
Istituto Pasteur, Fondazione Cenci-Bolognetti, Rome, Italy.
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MeSH Terms
Descriptor/Qualifier:
Animals
Chromosome Banding
Chromosomes / ultrastructure*
Drosophila melanogaster / genetics*
Female
In Situ Hybridization, Fluorescence / methods
Larva
Male
Mitotic Spindle Apparatus / ultrastructure*
Neurons

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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