POSSIBLE FUNCTION OF AH RECEPTOR NUCLEAR TRANSLOCATOR (ARNT) HOMODIMER IN TRANSCRIPTIONAL REGULATION

被引:172
作者
SOGAWA, K
NAKANO, R
KOBAYASHI, A
KIKUCHI, Y
OHE, N
MATSUSHITA, N
FUJIIKURIYAMA, Y
机构
[1] Department of Chemistry, Faculty of Science, Tohoku University, Aoba-ku
[2] Lab. for Genes of Motor Neurons, BioMimetic Control Research Center, Inst. of Phys. and Chemical Research, Atsuta-ku, Nagoya 456, 3-8-31, Rokuban
关键词
PAS DOMAIN; BASIC HELIX-LOOP-HELIX DOMAIN; P4501A1;
D O I
10.1073/pnas.92.6.1936
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Arnt (Ah receptor nuclear translocator) is a member of a transcription factor family having characteristic motifs designated bHLH (basic helix-loop-helix) and PAS and was originally found as a factor forming a complex with Ah receptor (AhR) to bind the specific xenobiotic responsive element (XRE) sequence for induction of drug-metabolizing P4501A1. We have examined interaction of Arnt with other PAS proteins-Drosophila Per, Sim, and AhR-by the coimmunoprecipitation method. Arnt formed a homodimer with itself as well as heterodimers with the others by means of the PAS and HLH domains in a cooperative way. The Arnt homodimer binds the sequence of adenovirus major late promoter (MLP) with the E box core sequence CACGTG, suggesting that the CAC half of the XRE, CACGCN(A/T), recognized by the AhR-Arnt heterodimer is a target for Arnt. Cotransfection experiments using CV-1 cells with an Arnt expression plasmid and a MLP chloramphenicol acetyltransferase (CAT) reporter plasmid revealed that Arnt markedly activated CAT expression, indicative of a newly discovered regulatory role of Arnt.
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页码:1936 / 1940
页数:5
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