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Science 23 January 1987:
Vol. 235. no. 4787, pp. 456 - 458
DOI: 10.1126/science.3099390

Articles

Science, Vol 235, Issue 4787, 456-458
Copyright © 1987 by American Association for the Advancement of Science


articles

In situ detection of beta-galactosidase in lenses of transgenic mice with a gamma-crystallin/lacZ gene

DR Goring, J Rossant, S Clapoff, ML Breitman, and LC Tsui

Transgenic mice carrying the gamma 2-crystallin promoter fused to the coding region of the bacterial lacZ gene were generated. The offspring of three founder mice expressed high levels of the enzyme solely in the central nuclear fiber cells of the lens as measured by an in situ assay for the detection of beta-galactosidase activity. These results suggest that gamma 2-crystallin sequences between -759 to +45 contain essential information required for appropriate tissue-specific and temporal regulation of the mouse gamma 2-crystallin gene. In a broader context, this study also demonstrates the utility of beta-galactosidase hybrid gene constructs for monitoring the activity of gene regulatory elements in transgenic mice.


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Retinal Expression of {gamma}-Crystallins in the Mouse.
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Transgenic animals.
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Genetic ablation: targeted expression of a toxin gene causes microphthalmia in transgenic mice.
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Expression and assembly of a human neurofilament protein in transgenic mice provide a novel neuronal marking system..
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Lens-specific enhancer in the third intron regulates expression of the chicken delta 1-crystallin gene..
S Hayashi, K Goto, T S Okada, and H Kondoh (1987)
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