Rescue of the lethal scl-/- phenotype by the human SCL locus

Angus M. Sinclair, Anthony J. Bench, Adrian J.C. Bloor, Juan Li, Berthold Göttgens, Maureen L. Stanley, Jane Miller, Sandra Piltz, Susie Hunter, Elisabeth P. Nacheva, María José Sanchez, Anthony R. Green

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)


The stem cell leukemia (SCL) gene encodes a basic helix-loop-helix transcription factor with a critical role in the development of both blood and endothelium. Loss-of-function studies have shown that SCL is essential for the formation of hematopoietic stem cells, for subsequent erythroid development and for yolk sac angiogenesis. SCL exhibits a highly conserved pattern of expression from mammals to teleost fish. Several murine SCL enhancers have been identified, each of which directs reporter gene expression in vivo to a subdomain of the normal SCL expression pattern. However, regulatory elements necessary for SCL expression in erythroid cells remain to be identified and the size of the chromosomal domain needed to support appropriate SCL transcription is unknown. Here we demonstrate that a 130-kilobase (kb) yeast artificial chromosome (YAC) containing the human SCL locus completely rescued the embryonic lethal phenotype of scl-/- mice. Rescued YAC+ scl-/- mice were born in appropriate Mendelian ratios, were healthy and fertile, and exhibited no detectable abnormality of yolk sac, fetal liver, or adult hematopoiesis. The human SCL protein can therefore substitute for its murine homologue. In addition, our results demonstrate that the human SCL YAC contains the chromosomal domain necessary to direct expression to the erythroid lineage and to all other tissues in which SCL performs a non-redundant essential function.

Original languageEnglish
Pages (from-to)3931-3938
Number of pages8
Issue number11
Publication statusPublished or Issued - 1 Jun 2002

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

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