Transcription of the lung-specific surfactant protein C gene is mediated by thyroid transcription factor 1

被引:203
|
作者
Kelly, SE [1 ]
Bachurski, CJ [1 ]
Burhans, MS [1 ]
Glasser, SW [1 ]
机构
[1] CHILDRENS HOSP,MED CTR,DIV PULM BIOL,TCHRF,CINCINNATI,OH 45229
关键词
D O I
10.1074/jbc.271.12.6881
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Surfactant protein C (SP-C) is expressed in alveolar Type II epithelial cells of the lung, In order to determine the mechanism(s) that regulate gene transcription, we have analyzed the activation of the murine SP-C promoter in mouse lung epithelial cells (RILE cells) and in HeLa cells after co-transfection with a vector expressing rat thyroid transcription factor-1 (TTF-1). TTF-1 transactivated SP-C-chloramphenicol acetyltransferase constructs containing -13 kilobase pairs to -320 base pairs (bp) of the 5' flanking region of the SP-C gene. Essential cis-acting elements were functionally localized to between -320 and -180 bp from the start of transcription by transfection analysis. Five DNase-protected regions, indicating multiple protein-DNA interactions within the -320 bp TTF-l-responsive region of the SP-C gene, were identified by I)Nase footprint analysis. A 40-bp segment of SP-C DNA from -197 to -158 linked to a heterologous promoter chloramphenicol acetyltransferase construct activated expression after co-transfection with CMV-TTF-1 in HeLa and RILE cells, The -197 to -158 segment contained two consensus TTF-1 sites, which were specifically identified as TTF-1 binding sites by gel retardation and antibody supershift with MLE cell nuclear extracts and purified TTF-1 homeodomain protein, Site-specific mutagenesis of either of the TTF-1 binding sites completely blocked activation by TTF-1, indicating both sites are required for TTF stimulation of SP-C transcription.
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页码:6881 / 6888
页数:8
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