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Molecular and Cellular Biology, February 2002, p. 946-952, Vol. 22, No. 3
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.22.3.946-952.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Jason W. Gill,1 Elise S. Randle-Barrett,1 Louise Barnett,2 Frank Koentgen,2,
Gavin W. Lambert,3 Richard P. Harvey,4,5 Richard L. Boyd,1 and Brendan J. Classon1
Department of Pathology and Immunology, Monash Medical School,1 Baker Medical Research Institute, Prahran, Victoria 3181,3 The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3050,2 Victor Chang Cardiac Research Institute, St. Vincents Hospital, Darlinghurst, New South Wales 2010,4 Departments of Medicine and Life Sciences, University of New South Wales, Kensington, New South Wales 2052, Australia5
Received 30 August 2001/ Accepted 30 October 2001
Thymic shared antigen 1 (TSA-1) is a plasma membrane protein of the Ly-6 superfamily expressed on thymocytes, thymic stromal cells, and other cells of the hematopoietic system. TSA-1 is also expressed in other nonhematopoietic tissues, in particular, embryonic and adult adrenal glands. To address the function of TSA-1, we generated mutant mice in which TSA-1 expression was inactivated by gene targeting. Here we show that deletion of both TSA-1 alleles results in abnormal adrenal gland development and midgestational lethality due to cardiac abnormalities. We also report that TSA-1-deficient adrenal glands have significantly reduced levels of the catecholamines noradrenaline and adrenaline. We conclude that TSA-1 is required for normal embryonic development but that deletion of its expression does not obviously impair lymphoid development.
Present address: Joslin Diabetes Center, Harvard Medical School, Boston, MA 01760.
Present address: Ozgene, Nedlands Campus, Nedlands, Western Australia 6009, Australia.
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