Transcriptional Repression of the Cystic Fibrosis Transmembrane Conductance Regulator Gene, Mediated by CCAAT Displacement Protein/cut Homolog, Is Associated with Histone Deacetylation
Human cystic fibrosis transmembrane conductance regulator gene ( CFTR ) transcription is tightly regulated by nucleotide sequences upstream of the initiator sequences. Our studies of human CFTR transcription focus on identifying transcription factors bound to an inverted CCAAT consensus or âY-box...
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Veröffentlicht in: | The Journal of biological chemistry 1999-03, Vol.274 (12), p.7803-7815 |
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Zusammenfassung: | Human cystic fibrosis transmembrane conductance regulator gene ( CFTR ) transcription is tightly regulated by nucleotide sequences upstream of the initiator sequences. Our studies of human CFTR transcription focus on identifying transcription factors bound to an inverted CCAAT consensus or âY-box element.â The human
homeodomain CCAAT displacement protein/ cut homolog (CDP /cut ) can bind to the Y-box element through a cut repeat and homeobox. Analysis of stably transfected cell lines with wild-type and mutant human CFTR -directed reporter genes demonstrates that human histone acetyltransferase GCN5 and transcription factor ATF-1 can potentiate
CFTR transcription through the Y-box element. We have found 1) that human CDP /cut acts as a repressor of CFTR transcription through the Y-box element by competing for the sites of transactivators hGCN5 and ATF-1; 2) that the ability
of CDP /cut to repress activities of hGCN5 and ATF-1 activity is contingent on the amount of CDP /cut expression; 3) that histone acetylation may have a role in the regulation of gene transcription by altering the accessibility
of the CFTR Y-box for sequence-specific transcription factors; 4) that trichostatin A, an inhibitor of histone deacetylase activity, activates
transcription of CFTR through the Y-box element; 5) that the inhibition of histone deacetylase activity leads to an alteration of local chromatin
structure requiring an intact Y-box sequence in CFTR ; 6) that immunocomplexes of CDP /cut possess an associated histone deacetylase activity; 7) that the carboxyl region of CDP /cut , responsible for the transcriptional repressor function, interacts with the histone deacetylase, HDAC1. We propose that CFTR transcription may be regulated through interactions with factors directing the modification of chromatin and requires the
conservation of the inverted CCAAT (Y-box) element of the CFTR promoter. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.274.12.7803 |