Bloom syndrome (BLM) is a genetic disorder-associated with predisposit
ion to cancer and chromosome instability. However, the most readily re
cognized clinical feature of the syndrome is growth retardation. Intro
duction of the previously cloned BLM gene into BLM cells yielded corre
ction of the chromosome instability and slow growth phenotypes. Additi
onally, asynchronous cultures of complemented clones revealed a lower
percentage of cells in S-phase than uncomplemented BLM cells. These re
sults support the notion that BLM is a defect in which short stature,
chromosome instability and cancer predisposition are all associated wi
th an error in DNA replication.