PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22)

• Published in: Genes chromosomes & cancer Vol. 40; no. 4; pp. 365 - 370
• Main Authors: Zhang, Yanming, Emmanuel, Neelmini, Kamboj, Ginny, Chen, Jianjun, Shurafa, Muhammad, Van Dyke, Daniel L., Wiktor, Anne, Rowley, Janet D.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.08.2004
• Subjects: Aged; Base Sequence - genetics; Chromosomes, Human, Pair 21 - genetics; Chromosomes, Human, X - genetics; Core Binding Factor Alpha 2 Subunit; Cytogenetic Analysis - methods; DNA-Binding Proteins - genetics; Exons - genetics; Humans; Karyotyping - methods; Leukemia, Myeloid, Acute - genetics; Male; Molecular Sequence Data; Neoplasm Proteins - genetics; Oncogene Proteins, Fusion - genetics; Peroxidases; Peroxiredoxins; Polymerase Chain Reaction - methods; Proto-Oncogene Proteins - genetics; Reading Frames - genetics; Transcription Factors - genetics; Translocation, Genetic - genetics
• ISSN: 1045-2257; 1098-2264
• DOI: 10.1002/gcc.20050

The AML1 gene (also known as RUNX1) at 21q22 codes for core binding factor (CBF) α, which forms a heterodimer with CBF β that acts as a transcriptional activating factor. CBF is a critical regulator in the generation and differentiation of definitive hematopoietic stem cells and is frequently disrupted in leukemia through chromosome translocations. We cloned a novel AML1 partner gene, PRDX4, in an X;21 translocation in a 74‐year‐old male patient diagnosed with acute myeloid leukemia–M2. Chromosome analysis detected a t(X;21)(p22;q22) as the sole abnormality in bone marrow samples. The involvement of AML1 was confirmed by fluorescence in situ hybridization studies. Using 3′ RACE‐PCR, we cloned a fusion between exon 5 of AML1 and exon 2 of PRDX4. RT‐PCR confirmed the fusion and detected another fusion between exon 6 of AML1 and exon 2 of PRDX4, indicating alternative splicing of exon 6 of AML1 in the fusion transcripts. PRDX4 is one of six peroxiredoxin‐family genes that are highly conserved in eukaryotes and prokaryotes and are ubiquitously expressed. Peroxiredoxin genes exhibit thioredoxin‐dependent peroxidase activity and have been implicated in a number of other cellular functions such as cell proliferation and differentiation. PRDX4 plays a regulatory role in the activation of the transcription factor NF‐κB and is significantly down‐regulated in acute promyelocytic leukemia. This is the first example of antioxidant enzyme involvement in a chromosome translocation in leukemia. © 2004 Wiley‐Liss, Inc.