Identification of transcripts modulated by ETV6 expression

G Boily, J Larose, S Langlois… - British journal of …, 2007 - Wiley Online Library
G Boily, J Larose, S Langlois, D Sinnett
British journal of haematology, 2007Wiley Online Library
Summary Deletions at chromosome 12p12‐13 are observed in 26–47% of childhood pre‐B
acute lymphoblastic leukaemia (ALL) cases, suggesting the presence of a tumour
suppressor gene (TSG). Accumulating genetic and functional evidence points to ETV6 as
being the most probable TSG targeted by the deletions. ETV6 is a ubiquitously expressed
transcription factor of the ETS family with very few known targets. To understand its function
and to elucidate the impact of its absence in leukaemia, we conducted a study to identify …
Summary
Deletions at chromosome 12p12‐13 are observed in 26–47% of childhood pre‐B acute lymphoblastic leukaemia (ALL) cases, suggesting the presence of a tumour suppressor gene (TSG). Accumulating genetic and functional evidence points to ETV6 as being the most probable TSG targeted by the deletions. ETV6 is a ubiquitously expressed transcription factor of the ETS family with very few known targets. To understand its function and to elucidate the impact of its absence in leukaemia, we conducted a study to identify targeted genes. Following the induction of ETV6 expression, global expression was evaluated at different time points. We identified 87 modulated genes, of which 10 (AKR1C1, AKR1C3, IL18, LUM, PHLDA1, PTGER4, PTGS2, SPHK1, TP53 and VEGF) were validated by real‐time quantitative reverse transcription‐polymerase chain reaction. To assess the significance of the validated candidate genes in leukaemia, their expression patterns were determined, as well as that of ETV6, in pre‐B ALL patients. The expression of IL18, LUM, PTGER4, SPHK1 and TP53 was significantly correlated with that of ETV6, further suggesting that ETV6 could regulate the expression of these genes in leukaemia. This work constitutes another step towards the understanding of the functions of ETV6 and the impact of its inactivation in childhood leukaemia.
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