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Dietary regulation of pancreatic amylase in transgenic mice mediated by a 126-base pair DNA fragment.

作者信息

Schmid R M, Meisler M H

机构信息

Department of Human Genetics, University of Michigan, Ann Arbor 48109-0618.

出版信息

Am J Physiol. 1992 Jun;262(6 Pt 1):G971-6. doi: 10.1152/ajpgi.1992.262.6.G971.

Abstract

Expression of the mouse pancreatic amylase gene Amy-2.2 is increased approximately 10-fold in response to increasing the carbohydrate content of the diet from 9.6 to 74%. The DNA sequence mediating this response has been localized to the 5' flanking region of the amylase gene by analysis of hybrid constructs in transgenic mice. The results define a 127-base pair dietary response unit that includes two previously described regulatory elements, an insulin-responsive element and a pancreatic enhancer. Fragments containing these two elements alone fail to respond to diet, demonstrating a requirement for additional regulatory sequences. Another mouse amylase gene Amy-2.1 is only minimally responsive to insulin and to diet. The data are consistent with the hypothesis that the insulin-response element is necessary but not sufficient for regulation of amylase by dietary carbohydrate.

摘要

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Dietary regulation of pancreatic amylase in transgenic mice mediated by a 126-base pair DNA fragment.
Am J Physiol. 1992 Jun;262(6 Pt 1):G971-6. doi: 10.1152/ajpgi.1992.262.6.G971.

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