TY - JOUR
T1 - Isolation and characterization of target sequences of the chicken CdxA homeobox gene
AU - Margalit, Yael
AU - Yarus, Sinai
AU - Shapira, Eli
AU - Gruenbaum, Yosef
AU - Fainsod, Abraham
N1 - Funding Information:
We wish to thank G.Pillemer for her comments on the manuscript. This work was supported by a grant from the Council for Tobacco Research, USA to A.Fainsod.
PY - 1993/10/25
Y1 - 1993/10/25
N2 - The DNA binding specificity of the chicken homeodomain protein CDXA was studied. Using a CDXAglutathione- S-tranferase fusion protein, DNA fragments containing the binding site for this protein were isolated. The sources of DNA were oligonucleotides with random sequence and chicken genomic DNA. The DNA fragments isolated were sequenced and tested in DNA bindin assays. Sequencing revealed that most DNA fragments are AT rich which is a common feature of homeodomain binding sites. B electrophoretic mobility shift assays it was shown that the different target sequences isolated bind to the CDXA protein with different affinities. The specific sequences bound by the CDXA protein in the genomic fragments isolated, were determined by DNase I footprinting. From the footprinted sequences, the CDXA consensus binding site was determined. The CDXA protein binds the consensus sequence A, A/T, T, A/T, A, T, A/G. The CAUDAL binding site in the ftz promoter is also included in this consensus sequence. When tested, some of the genomic target sequences were capable of enhancing the transcriptional activity of reporter plasmids when introduced into CDXA expressing cells. This study determined the DNA sequence specificity of the CDXA protein and it also shows that this protein can further activate transcription in cells in culture.
AB - The DNA binding specificity of the chicken homeodomain protein CDXA was studied. Using a CDXAglutathione- S-tranferase fusion protein, DNA fragments containing the binding site for this protein were isolated. The sources of DNA were oligonucleotides with random sequence and chicken genomic DNA. The DNA fragments isolated were sequenced and tested in DNA bindin assays. Sequencing revealed that most DNA fragments are AT rich which is a common feature of homeodomain binding sites. B electrophoretic mobility shift assays it was shown that the different target sequences isolated bind to the CDXA protein with different affinities. The specific sequences bound by the CDXA protein in the genomic fragments isolated, were determined by DNase I footprinting. From the footprinted sequences, the CDXA consensus binding site was determined. The CDXA protein binds the consensus sequence A, A/T, T, A/T, A, T, A/G. The CAUDAL binding site in the ftz promoter is also included in this consensus sequence. When tested, some of the genomic target sequences were capable of enhancing the transcriptional activity of reporter plasmids when introduced into CDXA expressing cells. This study determined the DNA sequence specificity of the CDXA protein and it also shows that this protein can further activate transcription in cells in culture.
UR - http://www.scopus.com/inward/record.url?scp=0027364769&partnerID=8YFLogxK
U2 - 10.1093/nar/21.21.4915
DO - 10.1093/nar/21.21.4915
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C2 - 7909943
AN - SCOPUS:0027364769
SN - 0305-1048
VL - 21
SP - 4915
EP - 4922
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 21
ER -