Zinc and cadmium can promote rapid nuclear translocation of metal response element-binding transcription factor-1 (Q28374397)

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R Ravindra

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H Jiang

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G K Andrews

Journal of Biological Chemistry

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language of work or name

English

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publication date

31 March 2000

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published in

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volume

275

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issue

13

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page(s)

9377-84

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cites work

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Reversible activation of mouse metal response element-binding transcription factor 1 DNA binding involves zinc interaction with the zinc finger domain

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Structural and functional heterogeneity among the zinc fingers of human MRE-binding transcription factor-1.

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MRE-Binding transcription factor-1: weak zinc-binding finger domains 5 and 6 modulate the structure, affinity, and specificity of the metal-response element complex

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The DNA binding activity of metal response element-binding transcription factor-1 is activated in vivo and in vitro by zinc, but not by other transition metals

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Embryonic lethality and liver degeneration in mice lacking the metal-responsive transcriptional activator MTF-1.

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Targeted disruption of metallothionein I and II genes increases sensitivity to cadmium

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Transition metals in control of gene expression

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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Regulation of metallothionein genes by heavy metals appears to be mediated by a zinc-sensitive inhibitor that interacts with a constitutively active transcription factor, MTF-1

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Cadmium-mediated activation of the metal response element in human neuroblastoma cells lacking functional metal response element-binding transcription factor-1

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A nuclear factor that interacts with metal responsive elements of a human metallothionein gene

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Immunocytochemical study of mammalian progesterone receptor using monoclonal antibodies

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cAMP stimulates the C/EBP-related transcription factor rNFIL-6 to trans-locate to the nucleus and induce c-fos transcription

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