Negative Regulatory Role of Sp1 in Metal Responsive Element-mediated Transcriptional Activation

Yasumitsu Ogra,Kaoru Suzuki,Pengfei Gong,Fuminori Otsuka,Shinji Koizumi

doi:10.1074/jbc.m100570200

Yasumitsu Ogra, Kaoru Suzuki + Show 3 more

Open Access

https://doi.org/10.1074/jbc.m100570200

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Abstract

Transcription of mammalian metallothionein (MT) genes is activated by heavy metals via multiple copies of a cis-acting DNA element, the metal-responsive element (MRE). Our previous studies have shown that certain MREs of the human MT-IIA gene (MREb, MREc, MREd, and MREf) are less active than the others (MREa, MREe, and MREg). Gel shift analysis of HeLa cell nuclear proteins revealed that whereas the active MREs strongly bind the transcription factor MTF-1 essential for metal regulation, the less active MREs bind another distinct protein, MREb-BF. This protein recognizes the GC-rich region of MREb rather than the MRE core required for MTF-1 binding. All the MREs recognized by MREb-BF contain the CGCCC and/or CACCC motif, suggesting that the MREb-BF.MRE complex contains Sp1 or related proteins. Supershift analysis using antibodies against Sp1 family proteins as well as gel shift analysis using the recombinant Sp1 demonstrated that Sp1 represents the majority of MREb-BF activity. An MREb mutant with reduced affinity to Sp1 mediated zinc-inducible transcription much more actively than the wild-type MREb. Furthermore, when placed in the native promoter, this mutant MREb raised the overall promoter activity. These results strongly suggest that Sp1 acts as a negative regulator of transcription mediated by specific MREs.

Highlights

Heavy metal-induced transcriptional activation of the genes coding for metallothioneins (MTs)1 is mediated by multiple copies of a cis-acting DNA element, the metal-responsive element (MRE; Refs. 1–3)
Three of these MREs (MREa, MREe, and MREg) efficiently mediate metal response of a reporter gene in transient transfection experiments and strongly bind the purified human MRE-binding transcription factor-1 (MTF-1) in vitro (11), consistent with the idea that MTF-1 plays the major role in metal-induced transcription (4, 5, 11)
MREb has extremely low activity when compared with the three active MREs, it is responsive to heavy metals and is able to bind MTF-1 (11)

Summary

Introduction

Heavy metal-induced transcriptional activation of the genes coding for metallothioneins (MTs)1 is mediated by multiple copies of a cis-acting DNA element, the metal-responsive element (MRE; Refs. 1–3). Three of these MREs (MREa, MREe, and MREg) efficiently mediate metal response of a reporter gene in transient transfection experiments and strongly bind the purified human MTF-1 in vitro (11), consistent with the idea that MTF-1 plays the major role in metal-induced transcription (4, 5, 11).

Results

Conclusion