The T-Cell Oncogenic Protein HOX11 ActivatesAldh1 Expression in NIH 3T3 Cells but Represses Its Expression in Mouse Spleen Development

ABSTRACT

Hox11 is a homeobox gene essential for spleen formation in mice, since atrophy of the anlage of a developing spleen occurs in early embryonic development in Hox11 null mice. HOX11 is also expressed in a subset of T-cell acute leukemias after specific chromosomal translocations. Since the protein has a homeodomain and can activate transcription, it probably exerts at least some of its effects in vivo by regulation of target genes. Representational difference analysis has been used to isolate cDNA clones corresponding to mRNA species activated following stable expression of HOX11 in NIH 3T3 cells. The gene encoding the retinoic acid-synthesizing enzyme aldehyde dehydrogenase 1 (Aldh1), initially called Hdg-1, was found to be ectopically activated by HOX11 in this system. Study ofAldh1 gene expression during spleen development showed that the presence of Aldh1 mRNA inversely correlated withHox11. Hox11 null mouse embryos have elevatedAldh1 mRNA in spleen primordia prior to atrophy, whileAldh1 seems to be repressed by Hox11 during organogenesis of the spleens of wild-type mice. This result suggests that expression of Aldh1 protein is negatively regulated by Hox11 and that abnormal expression of Aldh1 in Hox11 null mice may cause loss of splenic precursor cells by aberrant retinoic acid metabolism.

ACKNOWLEDGMENTS

We thank M. Hubank and D. Schatz for providing a detailed cDNA RDA protocol; L. Drynan, A. Forster, and I. Lavenir for technical help with this work; U. Kees for PER-117 and PER-255 cells; P. H. Rabbitts for LUDLU cells; and R. Hill for a Hox2.9 clone.

W.K.G. was the recipient of a C. J. Martin fellowship from the Australian National Health and Medical Research Council. N.M. was supported by the Leukaemia Research Fund.