We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
Mediator subunit MDT-15/MED15 and Nuclear Receptor HIZR-1/HNF4 cooperate to regulate toxic metal stress responses in Caenorhabditis elegans.
- Authors
Shomer, Naomi; Kadhim, Alexandre Zacharie; Grants, Jennifer Margaret; Cheng, Xuanjin; Alhusari, Deema; Bhanshali, Forum; Poon, Amy Fong-Yuk; Lee, Michelle Ying Ya; Muhuri, Anik; Park, Jung In; Shih, James; Lee, Dongyeop; Lee, Seung-Jae V.; Lynn, Francis Christopher; Taubert, Stefan
- Abstract
Zinc is essential for cellular functions as it is a catalytic and structural component of many proteins. In contrast, cadmium is not required in biological systems and is toxic. Zinc and cadmium levels are closely monitored and regulated as their excess causes cell stress. To maintain homeostasis, organisms induce metal detoxification gene programs through stress responsive transcriptional regulatory complexes. In Caenorhabditis elegans, the MDT-15 subunit of the evolutionarily conserved Mediator transcriptional coregulator is required to induce genes upon exposure to excess zinc and cadmium. However, the regulatory partners of MDT-15 in this response, its role in cellular and physiological stress adaptation, and the putative role for mammalian MED15 in the metal stress responses remain unknown. Here, we show that MDT-15 interacts physically and functionally with the Nuclear Hormone Receptor HIZR-1 to promote molecular, cellular, and organismal adaptation to cadmium and excess zinc. Using gain- and loss-of-function mutants and qRT-PCR and reporter analysis, we find that mdt-15 and hizr-1 cooperate to induce zinc and cadmium responsive genes. Moreover, the two proteins interact physically in yeast-two-hybrid assays and this interaction is enhanced by the addition of zinc or cadmium, the former a known ligand of HIZR-1. Functionally, mdt-15 and hizr-1 mutants show defective storage of excess zinc in the gut and are hypersensitive to zinc-induced reductions in egg-laying. Furthermore, mdt-15 but not hizr-1 mutants are hypersensitive to cadmium-induced reductions in egg-laying, suggesting potential divergence of regulatory pathways. Lastly, mammalian MDT-15 orthologs bind genomic regulatory regions of metallothionein and zinc transporter genes in a cadmium and zinc-stimulated fashion, and human MED15 is required to induce a metallothionein gene in lung adenocarcinoma cells exposed to cadmium. Collectively, our data show that mdt-15 and hizr-1 cooperate to regulate cadmium detoxification and zinc storage and that this mechanism is at least partially conserved in mammals. Author summary: In all life forms, zinc plays essential cellular and molecular roles. However, as with all molecules, excess zinc is hazardous, as is the presence of the physically and chemically highly similar cadmium. Organisms have evolved mechanisms to protect themselves against cadmium and high levels of zinc. Using the roundworm Caenorhabditis elegans, we previously showed that the Mediator subunit MDT-15 is essential in many cytoprotective response including that against excess zinc or cadmium. Here, we find that the nuclear receptor HIZR-1, shown previously to convey high zinc detoxification, works together with MDT-15 to protect worms against high zinc as well as cadmium by cooperatively activating a cytoprotective gene expression program. Notably, the two proteins bind physically in a fashion that is enhanced by exogenous zinc or cadmium; these molecules thus appear to act like stereotypical hormones by promoting a nuclear receptor–coregulator interaction. Exploring the evolutionary conservation of this mechanism, we find that MDT-15's orthologues bind and regulate zinc and cadmium responsive genes in mammalian cell lines. This provides the first evidence that mammalian MED15 functions in stress response pathways, establishing it as a cytoprotective regulator across eukaryotes.
- Subjects
HEAVY metals; CAENORHABDITIS elegans; CAENORHABDITIS; NUCLEAR receptors (Biochemistry); CADMIUM poisoning; ZINC transporters; PHYSIOLOGICAL stress; BIOLOGICAL systems
- Publication
PLoS Genetics, 2019, Vol 15, Issue 12, p1
- ISSN
1553-7390
- Publication type
Article
- DOI
10.1371/journal.pgen.1008508