Literature DB >> 15162037

Ionizing radiation-induced instant pairing of heterochromatin of homologous chromosomes in human cells.

H I Abdel-Halim1, S A Imam, F M Badr, A T Natarajan, L H F Mullenders, J J W A Boei.   

Abstract

Using fluorescence in situ hybridization with human band-specific DNA probes we examined the effect of ionizing radiation on the intra-nuclear localization of the heterochromatic region 9q12-->q13 and the euchromatic region 8p11.2 of similar sized chromosomes 9 and 8 respectively in confluent (G1) primary human fibroblasts. Microscopic analysis of the interphase nuclei revealed colocalization of the homologous heterochromatic regions from chromosome 9 in a proportion of cells directly after exposure to 4 Gy X-rays. The percentage of cells with paired chromosomes 9 gradually decreased to control levels during a period of one hour. No significant changes in localization were observed for chromosome 8. Using 2-D image analysis, radial and inter-homologue distances were measured for both chromosome bands. In unexposed cells, a random distribution of the chromosomes over the interphase nucleus was found. Directly after irradiation, the average inter-homologue distance decreased for chromosome 9 without alterations in radial distribution. The percentage of cells with inter-homologue distance <3 micro m increased from 11% in control cells to 25% in irradiated cells. In contrast, irradiation did not result in significant changes in the inter-homologue distance for chromosome 8. Colocalization of the heterochromatic regions of homologous chromosomes 9 was not observed in cells irradiated on ice. This observation, together with the time dependency of the colocalization, suggests an underlying active cellular process. The biological relevance of the observed homologous pairing remains unclear. It might be related to a homology dependent repair process of ionizing radiation induced DNA damage that is specific for heterochromatin. However, also other more general cellular responses to radiation-induced stress or change in chromatin organization might be responsible for the observed pairing of heterochromatic regions. Copyright 2003 S. Karger AG, Basel

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Year:  2004        PMID: 15162037     DOI: 10.1159/000077488

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  4 in total

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Authors:  Shamci Monajembashi; Alexander Rapp; Eberhard Schmitt; Heike Dittmar; Karl-Otto Greulich; Michael Hausmann
Journal:  Biophys J       Date:  2004-12-30       Impact factor: 4.033

2.  The STRUCTURAL MAINTENANCE OF CHROMOSOMES 5/6 complex promotes sister chromatid alignment and homologous recombination after DNA damage in Arabidopsis thaliana.

Authors:  Koichi Watanabe; Michael Pacher; Stefanie Dukowic; Veit Schubert; Holger Puchta; Ingo Schubert
Journal:  Plant Cell       Date:  2009-09-08       Impact factor: 11.277

3.  Random homologous pairing and incomplete sister chromatid alignment are common in angiosperm interphase nuclei.

Authors:  Veit Schubert; Young-Min Kim; Alexandre Berr; Jörg Fuchs; Armin Meister; Sylvia Marschner; Ingo Schubert
Journal:  Mol Genet Genomics       Date:  2007-05-24       Impact factor: 2.980

4.  1Q12 Loci Movement in the Interphase Nucleus Under the Action of ROS Is an Important Component of the Mechanism That Determines Copy Number Variation of Satellite III (1q12) in Health and Schizophrenia.

Authors:  Marina Sergeevna Konkova; Elizaveta Sergeevna Ershova; Ekaterina Alekseevna Savinova; Elena Mikhailovna Malinovskaya; Galina Vasilievna Shmarina; Andrey Vladimirovich Martynov; Roman Vladimirovich Veiko; Nataly Vyacheslavovna Zakharova; Pavel Umriukhin; Georgy Petrovich Kostyuk; Vera Leonidovna Izhevskaya; Sergey Ivanovich Kutsev; Natalia Nikolaevna Veiko; Svetlana Victorovna Kostyuk
Journal:  Front Cell Dev Biol       Date:  2020-06-05
  4 in total

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