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The Hox11 gene is essential for cell survival during spleen development.

TitleThe Hox11 gene is essential for cell survival during spleen development.
Publication TypeJournal Article
Year of Publication1995
AuthorsDear TN, Colledge WH, Carlton MB, Lavenir I, Larson T, Smith AG, Warren AJ, Evans MJ, Sofroniew MV, Rabbitts TH
Date Published1995 Sep
KeywordsAnimals, Apoptosis, Base Sequence, Gene Expression, Genes, Homeobox, Homeodomain Proteins, In Situ Hybridization, Leukemia, T-Cell, Mice, Mice, Mutant Strains, Molecular Sequence Data, Morphogenesis, Mutagenesis, Site-Directed, Oligonucleotide Probes, Oncogene Proteins, Spleen, Translocation, Genetic

The HOX11 homeobox gene was identified via the translocation t(10;14) in T cell leukaemia. To determine the function of this gene in mice, null mutations were made using homologous recombination in ES cells to incorporate lacZ into the hox11 transcription unit. Production of beta-galactosidase from the recombinant hox11 allele in +/- mutants allowed identification of sites of hox11 expression which included the developing spleen. Newborn hox11 -/- mice exhibit asplenia. Spleen formation commences normally at E11.5 in hox11 -/- mutant embryos but the spleen anlage undergoes rapid and complete resorption between E12.5 and E13.5. Dying spleen cells exhibit molecular features of apoptosis, suggesting that programmed cell death is initiated at this stage of organ development in the absence of hox11 protein. Thus hox11 is not required to initiate spleen development but is essential for the survival of splenic precursors during organogenesis. This function for hox11 suggests that enhanced cell survival may result from the t(10;14) which activates HOX11 in T cell leukaemias, further strengthening the association between oncogene-induced cell survival and tumorigenesis.

Alternate JournalDevelopment
PubMed ID7555717
Grant List / / Wellcome Trust / United Kingdom