The nuclear position of pericentromeric DNA of chromosome 11 appears to be random in G0 and non-random in G1 human lymphocytes

The nuclear topography of pericentromeric DNA of chromosome 11 was analyzed in G0 (nonstimulated) and G1 [phytohemagglutinin (PHA) stimulated] human lymphocytes by confocal microscopy. In addition to the nuclear center, the centrosome was used as a second point of reference in the three-dimensional...

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Bibliographic Details
Published inChromosoma Vol. 103; no. 4; p. 286
Main Authors Hulspas, R, Houtsmuller, A B, Krijtenburg, P J, Bauman, J G, Nanninga, N
Format Journal Article
LanguageEnglish
Published Austria 01.07.1994
Subjects
Cell Nucleus - metabolism
Cell Separation
Cells, Cultured
Centromere
Chromosomes, Human, Pair 11
DNA - metabolism
Flow Cytometry
G1 Phase
Humans
Lymphocytes - cytology
Lymphocytes - metabolism
Resting Phase, Cell Cycle
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Summary:The nuclear topography of pericentromeric DNA of chromosome 11 was analyzed in G0 (nonstimulated) and G1 [phytohemagglutinin (PHA) stimulated] human lymphocytes by confocal microscopy. In addition to the nuclear center, the centrosome was used as a second point of reference in the three-dimensional (3D) analysis. Pericentromeric DNA of chromosome 11 and the centrosome were labeled using a combination of fluorescent in situ hybridization (FISH) and immunofluorescence. To preserve the 3D morphology of the cells, these techniques were performed on whole cells in suspension. Three-dimensional images of the cells were analyzed with a recently developed 3D software program (Interactive Measurement of Axes and Positioning in 3 Dimensions). The distribution of the chromosome 11 centromeres appeared to be random during the G0 stage but clearly non-random during the G1 stage, when the nuclear center was used as a reference point. Further statistical analysis of the G1 cells revealed that the centromeres were randomly distributed in a shell underlying the nuclear membrane. A topographical relationship between the centrosome and the centromeres appeared to be absent during the G0 and G1 stages of the cell cycle.
ISSN:0009-5915