Chinese hamster cells (M3-1 line) in S phase were laser-UV-microirradiated (I, 257 nm) at a small site of the nucleus. Cells were fixed either immediately thereafter or in subsequent stages of the cell cycle, including prophase and metaphase. The microirradiated chromatin was visualized by indirect immunofluorescence microscopy using antibodies specific for UV-irradiated DNA. During the whole post-incubation period (4-15 h) immunofluorescent labelling was restricted to a small part of the nucleus (f, 4.5% of the total nuclear area). In mitotic cells segments of a few chromosomes only were labelled. Following microirradiation of chromosome segments in anaphase, immunofluorescent labelling was observed over a small part of the resulting interphase nucleus. A territorial organization of interphase chromosomes, i.e. interphase chromosomes occupying distinct domains, has previously been demonstrated by our group for the nucleus of Chinese hamster cells in Gl. Our present findings provide evidence that this organization pattern is maintained during the entire cell cycle.Evidence has recently been provided for a highly ordered arrangement of centromeres in metaphase plates of certain plant species [I]. Non-random arrangements of chromosomes have also been shown to a certain extent in metaphase plates of several mammalian species including man [2, 31. These findings have shed new light on the question of an ordered arrangement of interphase chromosomes as well, a question which still appears largely unsettled [3-71. Within this context it is important to know how the chromatin of individual chromosomes is distributed within the interphase nucleus at different stages of the cell cycle.In 1885, Rabl [8] suggested a model which predicts that interphase chromosomes maintain their anaphase-telophase orientation and occupy distinct nuclear