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Abstract
The GATA4 transcription factor is an important
developmental determinant for many organs such as the
heart, gut, and testis. Despite this pivotal role, our
understanding of the transcriptional mechanisms that
control the proper spatiotemporal expression of the
GATA4 gene remains limited. We have generated
transgenic mice expressing a green fluorescent protein
(GFP) marker under the control of rat Gata4 5'
flanking sequences. Several GATA4-expressing organs
displayed GFP fluorescence including the heart, intestine,
and pancreas. In the gonads, whereas GATA4 is expressed in
pregranulosa, granulosa and theca ovarian cells and
Sertoli, Leydig and peritubular testicular cells, the
first 5 kb of Gata4 regulatory sequences
immediately upstream of exon 1 were sufficient to direct
GFP reporter expression only in testis and specifically in
Sertoli cells. Onset of GFP expression occurred after
Sertoli cell commitment and was maintained in these cells
throughout development to adulthood. In vitro studies
revealed that the first 118 bp of the Gata4
promoter is sufficient for full basal activity in several
GATA4-expressing cell lines. Promoter mutagenesis and
DNA-binding experiments identified two GC-box motifs and
especially one E-box element within this -118 bp region
that are crucial for its activity. Further analysis
revealed that members of the USF family of transcription
factors, especially USF2, bind to and activate the
Gata4 promoter via this critical E-box motif.
Key words:
Testis
Developmental biology
Gene regulation
Sertoli cells
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