TY - JOUR
T1 - SMAD family member 3 (SMAD3) and SMAD4 repress HIF2-dependent iron-regulatory genes
AU - Ma, Xiaoya
AU - Das, Nupur K.
AU - Castillo, Cristina
AU - Gourani, Ayla
AU - Perekatt, Ansu O.
AU - Verzi, Michael P.
AU - Shah, Yatrik M.
N1 - Publisher Copyright:
© 2019 Ma et al. Published under exclusive license by The American Society for Biochemistry and Molecular Biology, Inc.
PY - 2019/3/15
Y1 - 2019/3/15
N2 - Hypoxia-inducible factor 2 (HIF2) directly regulates a battery of genes essential for intestinal iron absorption. Interestingly, iron deficiency and overload disorders do not result in increased intestinal expression of glycolytic or angiogenic HIF2 target genes. Similarly, inflammatory and tumor foci can induce a distinct subset of HIF2 target genes in vivo. These observations indicate that different stimuli activate distinct subsets of HIF2 target genes via mechanisms that remain unclear. Here, we conducted a high-throughput siRNA-based screen to identify genes that regulate HIF2’s transcriptional activity on the promoter of the iron transporter gene divalent metal transporter-1 (DMT1). SMAD family member 3 (SMAD3) and SMAD4 were identified as potential transcriptional repressors. Further analysis revealed that SMAD4 signaling selectively represses iron-absorptive gene promoters but not the inflammatory or glycolytic HIF2 or HIF1 target genes. Moreover, the highly homologous SMAD2 did not alter HIF2 transcriptional activity. During iron deficiency, SMAD3 and SMAD4 expression was significantly decreased via proteasomal degradation, allowing for derepression of iron target genes. Several iron-regulatory genes contain a SMAD-binding element (SBE) in their proximal promoters; however, mutation of the putative SBE on the DMT1 promoter did not alter the repressive function of SMAD3 or SMAD4. Importantly, the transcription factor forkhead box protein A1 (FOXA1) was critical in SMAD4-in-duced DMT1 repression, and DNA binding of SMAD4 was essential for the repression of HIF2 activity, suggesting an indirect repressive mechanism through DNA binding. These results provide mechanistic clues to how HIF signaling can be regulated by different cellular cues.
AB - Hypoxia-inducible factor 2 (HIF2) directly regulates a battery of genes essential for intestinal iron absorption. Interestingly, iron deficiency and overload disorders do not result in increased intestinal expression of glycolytic or angiogenic HIF2 target genes. Similarly, inflammatory and tumor foci can induce a distinct subset of HIF2 target genes in vivo. These observations indicate that different stimuli activate distinct subsets of HIF2 target genes via mechanisms that remain unclear. Here, we conducted a high-throughput siRNA-based screen to identify genes that regulate HIF2’s transcriptional activity on the promoter of the iron transporter gene divalent metal transporter-1 (DMT1). SMAD family member 3 (SMAD3) and SMAD4 were identified as potential transcriptional repressors. Further analysis revealed that SMAD4 signaling selectively represses iron-absorptive gene promoters but not the inflammatory or glycolytic HIF2 or HIF1 target genes. Moreover, the highly homologous SMAD2 did not alter HIF2 transcriptional activity. During iron deficiency, SMAD3 and SMAD4 expression was significantly decreased via proteasomal degradation, allowing for derepression of iron target genes. Several iron-regulatory genes contain a SMAD-binding element (SBE) in their proximal promoters; however, mutation of the putative SBE on the DMT1 promoter did not alter the repressive function of SMAD3 or SMAD4. Importantly, the transcription factor forkhead box protein A1 (FOXA1) was critical in SMAD4-in-duced DMT1 repression, and DNA binding of SMAD4 was essential for the repression of HIF2 activity, suggesting an indirect repressive mechanism through DNA binding. These results provide mechanistic clues to how HIF signaling can be regulated by different cellular cues.
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U2 - 10.1074/jbc.RA118.005549
DO - 10.1074/jbc.RA118.005549
M3 - Article
C2 - 30659096
AN - SCOPUS:85062982542
SN - 0021-9258
VL - 294
SP - 3974
EP - 3986
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 11
ER -