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(Received for publication, October 19, 1995; and in revised form, December 15, 1995) The promoter and its upstream regulatory region of the mouse
cellular retinoic acid-binding protein I (crabp-I) gene were
examined in transgenic mouse embryos, a mouse embryonal carcinoma cell
line P19, and a mouse embryonic fibroblast cell line 3T6. In transgenic
mouse embryos, a
Volume 271,
Number 9,
Issue of March 1, 1996 pp. 5073-5078
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
-galactosidase reporter gene under the control of crabp-I promoter and its upstream regulatory region displayed
a very specific pattern of expression characteristic of crabp-I gene expression during developmental stages. In tissue
culture systems, the minimal promoter of this gene was identified, and
regions containing positive and negative regulatory activities were
dissected from the upstream 3-kilobase sequence using assays for
transient reporter activity. It is concluded that the minimal promoter
of the mouse crabp-I gene is located between 120 and 150 base
pairs upstream from the transcription initiation site. Several cell
type-specific positive and negative regulatory regions for this
promoter have been identified. A region encoding a common negative
regulatory activity in both P19 and 3T6 cells is also inhibitory to two
heterologous promoters, and specific protein-DNA interactions between
this DNA fragment and nuclear extracts of P19 and 3T6 are demonstrated
by gel retardation experiments.
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