TY - JOUR
T1 - Upstream regions of the c-jun promoter regulate phorbol ester-induced transcription in U937 leukemic cells
AU - Unlap, Tino
AU - Franklin, Christopher C.
AU - Wagner, Fred
AU - Kraft, Andrew S.
N1 - Funding Information: We would like to thank Dr M.Karin for supplying the constructs which were necessary to begin this study. Dr Peter Angel was extremely helpful in first pointing out the uAP-1 sequence. This work was support by a PHS grant CA 42533 to A.S.K., and training grant CA09128 to C.C.F. and T.U.
PY - 1992/2/25
Y1 - 1992/2/25
N2 - To understand the mechanism by which phorbol esters (PMA) stimulate c-jun transcription In human leukemic cell line U937, we have mutated specific enhancer sequences within the c-jun promoter. We find in the region of DNA from -132 to +170 containing Sp1, C-TF and AP-1 sequences that mutation of the AP-1 sequence alone is not sufficient to abrogate transcription, and mutation of the Sp1 sequence Increases transcription 4-fold. Although mutation of the CTF site had no effect, CTF and AP-1 mutations together totally abrogate PMA-induced transcription. In comparison mutations of either of these sites alone or together in a construct containing -1639/ + 740 of the c-jun promoter had no effect on transcription. Because this data suggested the possibility of other upstream control regions, we sequenced the promoter from -142 to -1639. This sequence demonstrates a greater than 70% homology between human, and mouse c-jun promoters for the region from -142 to -441, and a second AP-1-like site In the -183 to -192 region. Mutation of this site did not influence transcription by PMA. By making constructs containing varying portions of the promoter, we have identified the region between -142 and - 711 to be responsible for mediating PMA-induced c-jun transcription.
AB - To understand the mechanism by which phorbol esters (PMA) stimulate c-jun transcription In human leukemic cell line U937, we have mutated specific enhancer sequences within the c-jun promoter. We find in the region of DNA from -132 to +170 containing Sp1, C-TF and AP-1 sequences that mutation of the AP-1 sequence alone is not sufficient to abrogate transcription, and mutation of the Sp1 sequence Increases transcription 4-fold. Although mutation of the CTF site had no effect, CTF and AP-1 mutations together totally abrogate PMA-induced transcription. In comparison mutations of either of these sites alone or together in a construct containing -1639/ + 740 of the c-jun promoter had no effect on transcription. Because this data suggested the possibility of other upstream control regions, we sequenced the promoter from -142 to -1639. This sequence demonstrates a greater than 70% homology between human, and mouse c-jun promoters for the region from -142 to -441, and a second AP-1-like site In the -183 to -192 region. Mutation of this site did not influence transcription by PMA. By making constructs containing varying portions of the promoter, we have identified the region between -142 and - 711 to be responsible for mediating PMA-induced c-jun transcription.
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U2 - 10.1093/nar/20.4.897
DO - 10.1093/nar/20.4.897
M3 - Article
C2 - 1542579
SN - 0305-1048
VL - 20
SP - 897
EP - 902
JO - Nucleic acids research
JF - Nucleic acids research
IS - 4
ER -