Two distal downstream enhancers direct expression of the human apolipoprotein E gene to astrocytes in the brain

S Grehan, E Tse, JM Taylor - Journal of Neuroscience, 2001 - Soc Neuroscience
S Grehan, E Tse, JM Taylor
Journal of Neuroscience, 2001Soc Neuroscience
Two distal downstream enhancers controlling astrocyte expression of the human
apolipoprotein E (apoE) gene in the brain were identified by analysis of transgenic mice
generated with various constructs of the apoE/CI/C-IV/C-II gene cluster. In wild-type mice,
the highest overall levels of apoE mRNA were found in astrocytes in the glomerular layer of
olfactory bulbs and in Bergmann glia in the cerebellum. This pattern of expression was
reproduced in transgenic mice expressing the entire human apoE gene cluster and also in …
Two distal downstream enhancers controlling astrocyte expression of the human apolipoprotein E (apoE) gene in the brain were identified by analysis of transgenic mice generated with various constructs of the apoE/C-I/C-IV/C-II gene cluster. In wild-type mice, the highest overall levels of apoE mRNA were found in astrocytes in the glomerular layer of olfactory bulbs and in Bergmann glia in the cerebellum. This pattern of expression was reproduced in transgenic mice expressing the entire human apoE gene cluster and also in transgenic mice expressing specific enhancer segments within the cluster. Expression of the human apoE transgene at these sites was specified by two enhancer domains: one enhancer is located 3.3 kb downstream of the apoE gene, and a duplication of this sequence is located 15 kb downstream of the apoE gene. Astrocyte enhancer activity was contained within 620 and 619 bp segments of these domains that show subtle differences in regional expression. In the absence of these distal enhancers, the apoE gene was not expressed in astrocytes. The relatively high levels of apoE expression at specific sites in the olfactory bulb and cerebellum suggest the presence of unique regulatory signals at these locations that may reflect common cellular properties and apoE gene functions. The localization of the two astrocytic enhancers reveals an unexpected complexity in the control of apoE production that is essential to understanding apoE function in the brain.
Soc Neuroscience