Premium
Novel alternative PBX3 isoforms in leukemia cells with distinct interaction specificities
Author(s) -
Milech Nadia,
Kees Ursula R.,
Watt Paul M.
Publication year - 2001
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/gcc.1190
Subject(s) - gene isoform , biology , gene , haematopoiesis , leukemia , homeobox , genetics , homology (biology) , alternative splicing , computational biology , cancer research , transcription factor , stem cell
PBX3 is a member of the PBX family of TALE homeobox genes. The prototypic member, PBX1 , was first identified in chromosomal translocations in B‐lineage leukemia and is required for normal hematopoiesis. PBX2 and PBX3 were later identified as members of this highly conserved family by their strong homology to PBX1 . While the expression pattern of PBX1 is restricted, PBX2 and PBX3 are ubiquitously expressed. Little is known about the functional role of PBX3 . Our studies identified two PBX3 transcripts alternative to the canonical forms, PBX3A and PBX3B, resulting from a novel splice in PBX3 . These new isoforms, named PBX3C and PBX3D , have been detected in all tissues and cell lines tested. Intriguingly, expression of PBX3D is favored in normal cells, whereas PBX3C expression is favored in leukemia cells. Functional studies showed that PBX3C and PBX3D proteins were unable to interact with the PBX‐interacting factor PREP1 and weakly interacted with MEIS proteins. We propose that PBX3C and PBX3D may affect PBX3‐mediated transcriptional regulation by acting in opposition to the known PBX proteins through alternative PBX3 complex formation. The identification and characterization of these novel PBX3 isoforms provide a foundation for a better understanding of the biological role of PBX3 . © 2001 Wiley‐Liss, Inc.