SCL and LMO1 alter thymocyte differentiation: inhibition of E2A-HEB function and pre-Tα chain expression

S Herblot, AM Steff, P Hugo, PD Aplan, T Hoang - Nature immunology, 2000 - nature.com
S Herblot, AM Steff, P Hugo, PD Aplan, T Hoang
Nature immunology, 2000nature.com
Cooperation between the stem cell leukemia (SCL) transcription factor and its nuclear
partners LMO1 or LMO2 induces aggressive T cell acute lymphoblastic leukemia when
inappropriately expressed in T cells. This study examined the cellular and molecular targets
of the SCL-LMO complex at the pre-leukemic stage. We show that SCL and its partners are
coexpressed in the most primitive thymocytes. Maturation to the pre-T cell stage is
associated with a down-regulation of SCL and LMO1 and LMO2, and a concomitant up …
Abstract
Cooperation between the stem cell leukemia (SCL) transcription factor and its nuclear partners LMO1 or LMO2 induces aggressive T cell acute lymphoblastic leukemia when inappropriately expressed in T cells. This study examined the cellular and molecular targets of the SCL-LMO complex at the pre-leukemic stage. We show that SCL and its partners are coexpressed in the most primitive thymocytes. Maturation to the pre-T cell stage is associated with a down-regulation of SCL and LMO1 and LMO2, and a concomitant up-regulation of E2A and HEB expression. Moreover, enforced expression of SCL-LMO1 inhibits T cell differentiation and recapitulates a loss of HEB function, causing a deregulation of the transition checkpoint from the CD4− CD8− to CD4+ CD8+ stages. Finally, we identify the gene encoding pTα as a downstream target of HEB that is specifically repressed by the SCL-LMO complex.
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