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Molecular and Cellular Biology, October 2007, p. 7236-7247, Vol. 27, No. 20
0270-7306/07/$08.00+0 doi:10.1128/MCB.00780-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
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Department of Molecular Physiology and Biophysics,1 Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas 770302
Received 3 May 2007/ Returned for modification 4 June 2007/ Accepted 7 August 2007
The size of an organ must be tightly controlled so that it fits within an organism. The mammalian lens is a relatively simple organ composed of terminally differentiated, amitotic lens fiber cells capped on the anterior surface by a layer of immature, mitotic epithelial cells. The proliferation of lens epithelial cells fuels the growth of the lens, thus controling the size of the lens. We report that the Notch signaling pathway defines the boundary between proliferation and differentiation in the developing lens. The loss of Notch signaling results in the loss of epithelial cells to differentiation and a much smaller lens. We found that the Notch effector Herp2 is expressed in lens epithelium and directly suppresses p57Kip2 expression, providing a molecular link between Notch signaling and the cell cycle control machinery during lens development.
Published ahead of print on 20 August 2007.
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