Structure and expression of the mouse AhR nuclear translocator (mArnt) gene

Feng Wang, Jin Xou Gao, Junsei Mimura, Akira Kobayashi, Kazuhiro Sogawa, Yoshiaki Fujii-Kuriyama

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Aryl hydrocarbon receptor (AhR) nuclear translocator (Arnt) gene has been isolated and characterized from a mouse genomic DNA library. The gene is about 60 kilobases long and split into 22 exons. An unusual exon/intron junctional sequence was found in the 11th intron of the gene that begins with GC at its 5'-end. The exon/intron arrangement of mArnt gene differs greatly from those of the other members of the same basic-helix-loop-helix/PAS family. The gene is TATA-less and has several transcription start sites. The promoter region of the mArnt gene is GC-rich and contains a number of putative regulatory DNA sequences such as two GC-boxes, a cAMP-responsive element, E-box, AP-1 site, and CAAT-box. Deletion experiments revealed that all these DNA elements made substantial contributions to a high level of expression of the gene, except for the cAMP-responsive element. Of all, two GC-boxes displayed the most dominant enhancing effects. It was demonstrated that there exist specific factors binding to these DNA elements in the nuclear extracts of HeLa cells. Among them, Sp1 and Sp3, and CAAT-box binding factor-A were identified to bind the GC-boxes nd CAAT-box, respectively. Expression of MyoD in HeLa cells stimulated the Arnt promoter activity by binding to the E-box.

Original languageEnglish
Pages (from-to)24867-24873
Number of pages7
JournalJournal of Biological Chemistry
Volume273
Issue number38
DOIs
Publication statusPublished - 1998 Sept 18
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Fingerprint

Dive into the research topics of 'Structure and expression of the mouse AhR nuclear translocator (mArnt) gene'. Together they form a unique fingerprint.

Cite this