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(Received for publication, May 13, 1996, and in revised form, June 26, 1996)
From the Groupe de Recherche en Oncogénétique,
Département de Pathologie, Université de
Montréal, Montréal, Québec, Canada H3C 3J7
Three proximal elements, PER1, PER2, and PER3,
have been implicated in the regulation of peripherin gene expression.
PER1 contains the TATA motif and was identified as the principal
mediator of neuronal specificity. Here, we demonstrate by transfection
of constructs mutated in PER1 that the in vitro protein
binding activity of PER1 is irrelevant to its function. However,
mutations or substitutions in the TATA box decreased promoter activity
by up to 80%. We have investigated this unusual preference for a
particular TATA sequence in PC12 cells. In these cells, nerve growth
factor induces neuronal differentiation, increasing peripherin gene
expression 3-4-fold, while dexamethasone elicits chromaffin
differentiation and a 3-fold decrease in peripherin mRNA.
Experiments with stably transfected PC12 cells revealed that the
specific TATA box of the peripherin gene was crucial for nerve growth
factor response. However, it did not affect dexamethasone
down-regulation. Therefore, nerve growth factor acts through an element
essential for neuronal peripherin gene expression. The results predict
that proteins interacting in the vicinity of the TATA box, by inference
factors associated with the preinitiation complex, are important for
peripherin gene regulation and provide new insights into the mechanisms
underlying neuronal differentiation.
Volume 271, Number 40,
Issue of October 4, 1996
pp. 24976-24981
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
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