Interactive computer-assisted analysis of chromosome 1 colocalization with nucleoli.

The applications of DNA cloning and fluorescent in situ hybridization (FISH) techniques have strengthened the hypothesis of an ordered chromatin structure in interphase nuclei, strongly suspected to vary with functional state. The nonrandom distribution of the centromeres and their dynamic rearrangement during the cell cycle have been well documented. A close proximity of specific centromeres to nucleoli has also been reported, but the functional meaning of this association is still unknown. In order to investigate whether the chromosome 1 centromere region to nucleolus association depends on the cell cycle and chromosome status, we combined FISH of probes specific for the 1q12 region with Ki-67 nucleolar antigen fluorescent immunocytochemical (FICC) detection on the MCF-7 human breast cancer cell line and on the MRC-5 normal fibroblastic cell line. Both FISH and FICC signals were interactively localized in a one-step fluorescent microscopic observation and further analyzed using the Highly Optimized Microscope Environment (HOME) graphics microscope workstation, which provided computerized interactive marking of 1q12 to nucleolus associations (1q12-nu) at the individual nucleus and nucleolus levels. This study confirms that centromeric regions, other than those adjacent to the major ribosomal cistrons, contribute to the perinucleolar chromatin and demonstrate that, during the cell cycle, the heterochromatic band 1q12 is dynamically rearranged with regard to both the nuclear volume and the nucleoli. A relationship between the association of the chromosome 1 pericentromeric region with nucleoli and the nucleolar transcriptional activity is also strongly suggested.

[1]  G. Brugal,et al.  Detection of chromosome 1 aberrations by fluorescent in situ hybridization (FISH) in the human breast cancer cell line MCF-7. , 1993, Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology.

[2]  D. Hernandez-Verdun,et al.  Behaviour of nucleolar proteins in nuclei lacking ribosomal genes. A study by confocal laser scanning microscopy. , 1991, Journal of cell science.

[3]  L. Manuelidis,et al.  Movement of the X chromosome in epilepsy. , 1988, Science.

[4]  R. Ochs,et al.  Centromere autoantigens are associated with the nucleolus. , 1992, Experimental cell research.

[5]  E. Tan,et al.  Distribution of kinetochore (centromere) antigen in mammalian cell nuclei , 1981, The Journal of cell biology.

[6]  R. Nardone,et al.  Cyclic nucleolar changes during the cell cycle. I. Variations in number, size, morphology and position. , 1968, Experimental cell research.

[7]  G Brugal,et al.  HOME: highly optimized microscope environment. , 1992, Cytometry.

[8]  H. Willard,et al.  Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes. , 1988, Cancer research.

[9]  C Cremer,et al.  Distribution of chromosome 18 and X centric heterochromatin in the interphase nucleus of cultured human cells. , 1990, Experimental cell research.

[10]  A. Jauch,et al.  Double in situ hybridization in combination with digital image analysis: a new approach to study interphase chromosome topography. , 1989, Experimental cell research.

[11]  C. Steinlein,et al.  Nucleolar transcriptional activity in mouse Sertoli cells is dependent on centromere arrangement. , 1990, Experimental cell research.

[12]  L. Manuelidis Different central nervous system cell types display distinct and nonrandom arrangements of satellite DNA sequences. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[13]  N. Ringertz,et al.  Direct evidence for the non-random localization of mammalian chromosomes in the interphase nucleus. , 1986, Experimental cell research.

[14]  D. Seigneurin,et al.  Quantification and topographical description of Ki-67 antibody labelling during the cell cycle of normal fibroblastic (MRC-5) and mammary tumour cell lines (MCF-7). , 1989, Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology.

[15]  D. Ward,et al.  Cell cycle-dependent distribution of telomeres, centromeres, and chromosome-specific subsatellite domains in the interphase nucleus of mouse lymphocytes. , 1993, Experimental cell research.

[16]  E. Tan,et al.  Kinetochore structure, duplication, and distribution in mammalian cells: analysis by human autoantibodies from scleroderma patients , 1981, The Journal of cell biology.

[17]  A. Raap,et al.  Denaturation, renaturation, and loss of DNA during in situ hybridization procedures. , 1986, Cytometry.

[18]  M. Bartholdi,et al.  Nuclear distribution of centromeres during the cell cycle of human diploid fibroblasts. , 1991, Journal of cell science.

[19]  J. Hindley,et al.  Cloning of human satellite III DNA: different components are on different chromosomes. , 1979, Nucleic acids research.

[20]  J. Steitz,et al.  A 5S rRNA/L5 complex is a precursor to ribosome assembly in mammalian cells , 1988, The Journal of cell biology.

[21]  W. Prensky,et al.  Localisation of 5S ribosomal RNA genes on human chromosome 1 , 1974, Nature.