TY - JOUR
T1 - Sequences of the 5′ portion of the human c-sis gene
T2 - Characterization of the transcriptional promoter and regulation of expression of the protein product by 5' untranslated mRNA sequences
AU - Ratner, Lee
AU - Thielan, Benjamin
AU - Collins, Tucker
N1 - Funding Information:
OCKNOWLEDGEMENTS We thank S. Josephs and B. Hahn for providing high molecular weight samples, P. Reddy for the oligonucleotide probe, J. Boss for assistance with the i_n vi.t.ro transcription reactions, D. Tanen and P. Riendeau for technical assistance, and J. Pober and S. Orkin for enthusiastic support. This work was supported by a contractural agreement between Washington University and the Monsanto Co., by an institutional American Cancer Society grant to Washington University, and by NIH grant HL35716 to T.C. L.R. is a Hartford Foundation fellow.
PY - 1987/8/11
Y1 - 1987/8/11
N2 - The c-sis gene encodes the B polypeptide chain of plateletderived growth factor (PDGF), and is expressed in a number of normal and pathological conditions. In order to study the control of synthesis of the human c-sis product, we have initiated a study of two regions of this genetic locus which regulate transcription and translation. A clone of the 5' portion of the gene was obtained which included 1361 nucleotides upstream of the RNA initiation site. Transcriptional promoter activity of this region was demonstrated in normal and transformed cells using a plasmid with the sequences upstream of the c-sis RNA initiation site fused to an indicator gene, chloramphenicol acetyl transferase. Experiments were also performed to identify other possible regulatory regions of the c-sis gene. These data demonstrated that a portion of the c-sis first exon encoding the 5' untranslated region of the c-sis mRNA inhibited synthesis of the PDGF B product in vitro. These results define regions of the c-sis gene whose activity may be important in the regulation of transcription and translation under normal conditions and in the pathogenesis several human diseases.
AB - The c-sis gene encodes the B polypeptide chain of plateletderived growth factor (PDGF), and is expressed in a number of normal and pathological conditions. In order to study the control of synthesis of the human c-sis product, we have initiated a study of two regions of this genetic locus which regulate transcription and translation. A clone of the 5' portion of the gene was obtained which included 1361 nucleotides upstream of the RNA initiation site. Transcriptional promoter activity of this region was demonstrated in normal and transformed cells using a plasmid with the sequences upstream of the c-sis RNA initiation site fused to an indicator gene, chloramphenicol acetyl transferase. Experiments were also performed to identify other possible regulatory regions of the c-sis gene. These data demonstrated that a portion of the c-sis first exon encoding the 5' untranslated region of the c-sis mRNA inhibited synthesis of the PDGF B product in vitro. These results define regions of the c-sis gene whose activity may be important in the regulation of transcription and translation under normal conditions and in the pathogenesis several human diseases.
UR - http://www.scopus.com/inward/record.url?scp=0023651121&partnerID=8YFLogxK
U2 - 10.1093/nar/15.15.6017
DO - 10.1093/nar/15.15.6017
M3 - Article
C2 - 3627977
AN - SCOPUS:0023651121
SN - 0305-1048
VL - 15
SP - 6017
EP - 6036
JO - Nucleic acids research
JF - Nucleic acids research
IS - 15
ER -