Chapter 27. The LMO2 Master Gene; Its Role as a Transcription Regulator Determining Cell Fate in Leukemogenesis and in Hematopoiesis

  1. Katya Ravid2,
  2. Jonathan D. Licht3
  1. Yoshihiro Yamada,
  2. Terence H. Rabbitts

Published Online: 19 MAR 2002

DOI: 10.1002/0471223883.ch27

Transcription Factors: Normal and Malignant Development of Blood Cells

Transcription Factors: Normal and Malignant Development of Blood Cells

How to Cite

Yamada, Y. and Rabbitts, T. H. (2002) The LMO2 Master Gene; Its Role as a Transcription Regulator Determining Cell Fate in Leukemogenesis and in Hematopoiesis, in Transcription Factors: Normal and Malignant Development of Blood Cells (eds K. Ravid and J. D. Licht), John Wiley & Sons, Inc., New York, USA. doi: 10.1002/0471223883.ch27

Editor Information

  1. 2

    Department of Biochemistry, Boston University School of Medicine, Boston, MA

  2. 3

    Derald H. Ruttenberg Cancer Center and Department of Medicine, Mount Sinai School of Medicine, New York, NY

Author Information

  1. MRC Laboratory of Molecular Biology, Division of Protein and Nucleic Acid Chemistry, Hills Road, Cambridge CB2 2QH, UK

Publication History

  1. Published Online: 19 MAR 2002
  2. Published Print: 15 DEC 2000

ISBN Information

Print ISBN: 9780471350545

Online ISBN: 9780471223887

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Keywords:

  • Lmo2 master gene;
  • chromosomal translocations;
  • transcription regulator;
  • developmental regulation;
  • cell fate;
  • Lmo2 protein;
  • T-cell acute leukemia;
  • hematopiesis

Summary

The LMO2 gene typifies the type of gene associated with chromosomal translocation breakpoints in acute leukemia. This gene encodes a protein that displays features of a transcriptional regulator, a developmental regulator and a master gene regulator, as proposed previously for chromosomal translocation genes in acute tumors. In this chapter the authors summarize data illustrating these points, which show the normal role of Lmo2 in hematopoiesis and vascular formation and the aberrant role in the development of T cells prior to tumor formation.