Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 11 May 2007:
Vol. 316. no. 5826, pp. 860 - 866
DOI: 10.1126/science.1140881

Research Articles

Regulation of B Versus T Lymphoid Lineage Fate Decision by the Proto-Oncogene LRF

Takahiro Maeda,1* Taha Merghoub,1 Robin M. Hobbs,1 Lin Dong,1 Manami Maeda,1* Johannes Zakrzewski,2 Marcel R.M. van den Brink,2 Arthur Zelent,4 Hirokazu Shigematsu,5 Koichi Akashi,5 Julie Teruya-Feldstein,3 Giorgio Cattoretti,6{dagger} Pier Paolo Pandolfi1,3{ddagger}

Hematopoietic stem cells in the bone marrow give rise to lymphoid progenitors, which subsequently differentiate into B and T lymphocytes. Here we show that the proto-oncogene LRF plays an essential role in the B versus T lymphoid cell-fate decision. We demonstrate that LRF is key for instructing early lymphoid progenitors in mice to develop into B lineage cells by repressing T cell–instructive signals produced by the cell-fate signal protein, Notch. We propose a new model for lymphoid lineage commitment, in which LRF acts as a master regulator of the cell's determination of B versus T lineage.

1 Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
2 Department of Medicine and Immunology Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
3 Department of Pathology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
4 Leukemia Research Fund Center at the Institute of Cancer Research, Chester Beatty Laboratories, Fulham Road, London SW3 6JB, London, UK.
5 Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Smith Building 770A, 1 Jimmy Fund Way, Boston, MA 02115, USA
6 Institute for Cancer Genetics, Columbia University, New York, NY 10032 USA.

* Present address: Department of Hematopoietic Stem Cell and Leukemia Research, City of Hope National Medical Center, 1500 East Duarte Road, Duarte, CA 91010, USA.

{dagger} Present address: Department of Pathology, Università degli Studi Milano-Bicocca and Azienda Ospedaliera San Gerardo, Via Pergolesi 33, 20052 Monza (MI), Italy.

{ddagger} To whom correspondence should be addressed. E-mail: p-pandolfi{at}ski.mskcc.org

Read the Full Text



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
A Novel POK Family Transcription Factor, ZBTB5, Represses Transcription of p21CIP1 Gene.
D.-I. Koh, W.-I. Choi, B.-N. Jeon, C.-E. Lee, C.-O. Yun, and M.-W. Hur (2009)
J. Biol. Chem. 284, 19856-19866
   Abstract »    Full Text »    PDF »
Proto-oncogene FBI-1 Represses Transcription of p21CIP1 by Inhibition of Transcription Activation by p53 and Sp1.
W.-I. Choi, B.-N. Jeon, C.-O. Yun, P.-H. Kim, S.-E. Kim, K.-Y. Choi, S. H. Kim, and M.-W. Hur (2009)
J. Biol. Chem. 284, 12633-12644
   Abstract »    Full Text »    PDF »
An early decrease in Notch activation is required for human TCR-{alpha}{beta} lineage differentiation at the expense of TCR-{gamma}{delta} T cells.
I. Van de Walle, G. De Smet, M. De Smedt, B. Vandekerckhove, G. Leclercq, J. Plum, and T. Taghon (2009)
Blood 113, 2988-2998
   Abstract »    Full Text »    PDF »
Ikaros Regulates Notch Target Gene Expression in Developing Thymocytes.
S. Chari and S. Winandy (2008)
J. Immunol. 181, 6265-6274
   Abstract »    Full Text »    PDF »
Delta-like 4 is indispensable in thymic environment specific for T cell development.
K. Hozumi, C. Mailhos, N. Negishi, K.-i. Hirano, T. Yahata, K. Ando, S. Zuklys, G. A. Hollander, D. T. Shima, and S. Habu (2008)
J. Exp. Med. 205, 2507-2513
   Abstract »    Full Text »    PDF »
Proto-oncogene FBI-1 (Pokemon) and SREBP-1 Synergistically Activate Transcription of Fatty-acid Synthase Gene (FASN).
W.-I. Choi, B.-N. Jeon, H. Park, J.-Y. Yoo, Y.-S. Kim, D.-I. Koh, M.-H. Kim, Y.-R. Kim, C.-E. Lee, K.-S. Kim, et al. (2008)
J. Biol. Chem. 283, 29341-29354
   Abstract »    Full Text »    PDF »
Why T Cells of Thymic Versus Extrathymic Origin Are Functionally Different.
M.-E. Blais, S. Brochu, M. Giroux, M.-P. Belanger, G. Dulude, R.-P. Sekaly, and C. Perreault (2008)
J. Immunol. 180, 2299-2312
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)