Telomeres are specialized structures at chromosome ends that are thoug
ht to function as buffers against chromosome fusion. Several studies s
uggest that telomere shortening may render chromosomes fusigenic. We u
sed a novel quantitative fluorescence in situ hybridization procedure
to estimate telomere length in individual mammalian chromosomes, and G
-banding and chromosome painting techniques to determine chromosome fu
sigenic potential. All analysed Chinese hamster and mouse cell lines e
xhibited shorter telomeres at short chromosome arms than at long chrom
osome arms. However, no clear link between short telomeres and chromos
ome fusigenic potential was observed, i.e. frequencies of telomeric as
sociations were higher in cell lines exhibiting longer telomeres. We s
peculate that chromosome fusigenic potential in mammalian cell lines m
ay be determined not only by telomere length but also by the status of
telomere chromatin structure. This is supported by the observed prese
nce of chromatin filaments linking telomeres in Chinese hamster chromo
somes and of multibranched chromosomes oriented end-to-end in the muri
ne severe combined immunodeficient (SCID) cell line. Multibranched chr
omosomes are the hallmark of the human ICF (Immune deficiency, Centrom
eric instability, Facial abnormalities) syndrome, characterized by alt
erations in heterochromatin structure.