A study by Bose and colleagues [(1998). Blood 92:3362–3367] and a previous study by Biernaux and others [(1996). Bone Marrow Transplant 17:(Suppl. 3) S45–S47] showed that BCR-ABL fusion gene transcripts can be detected in 25 to 30 percent of healthy adults who do not develop chronic myelogenous leukemia (CML). Explain how these individuals can carry a fusion gene that is transcriptionally active and yet do not develop CML.

Key Concepts

BCR-ABL Fusion Gene

The BCR-ABL fusion gene results from a chromosomal translocation between the BCR gene on chromosome 22 and the ABL gene on chromosome 9. This fusion creates a hybrid protein that has tyrosine kinase activity, which can lead to uncontrolled cell proliferation. However, the presence of this gene alone does not guarantee the development of chronic myelogenous leukemia (CML), as other genetic and environmental factors also play a crucial role in disease manifestation.

Transcriptional Activity

Transcriptional activity refers to the process by which a gene is expressed to produce RNA, which can then be translated into proteins. In the case of the BCR-ABL fusion gene, it can be actively transcribed in some individuals without leading to CML. This suggests that while the gene is present and functional, additional mutations or regulatory mechanisms may be necessary for the progression to leukemia.

Genetic and Environmental Factors

The development of diseases like CML is influenced by a combination of genetic predispositions and environmental factors. While the presence of the BCR-ABL fusion gene is a significant risk factor, not all individuals with this gene develop CML. Factors such as additional genetic mutations, immune system status, and exposure to certain environmental triggers can determine whether an individual progresses to leukemia despite having an active fusion gene.