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J Biol Chem, Vol. 274, Issue 7, 4328-4334, February 12, 1999
From the Institute of Biomedical and Life Sciences, Division of
Biochemistry and Molecular Biology, Davidson Building, University
of Glasgow, Glasgow G12 8QQ, United Kingdom
Dramatic changes in the patterns of transcription
are a common feature of early development. We have used F9 embryonal
carcinoma cells as a model system to study gene regulation during an
early stage of murine embryogenesis. We find that transcription by RNA polymerase I decreases when F9 cells differentiate into parietal endoderm. The reduced rate of transcription is associated with a
down-regulation of several components of the class I transcription apparatus. The most substantial change involves the essential factor
SL1, which is a multisubunit complex that contains the TATA-binding
protein and three TATA-binding protein-associated factors (TAFs). The
abundance of two of these TAFs, TAFI48 and TAFI95, decreases during F9 cell differentiation.
Developmental regulation of a specific class of genes may therefore be
achieved through changes in the availability of TAFs.
Regulation of RNA Polymerase I Transcription in Response to
F9 Embryonal Carcinoma Stem Cell Differentiation
Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.
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