Iron-mediated post-transcriptional regulation in Toxoplasma gondii

Iron is required to support almost all life; however, levels must be carefully regulated to maintain homeostasis. Although the obligate parasite Toxoplasma gondii requires iron, how it responds upon iron limitation has not been investigated. Here, we show that iron depletion triggers significant transcriptional changes in the parasite, including in iron-dependent pathways. We find that a subset of T. gondii transcripts contain stem-loop structures, which have been associated with post-transcriptional iron-mediated regulation in other cellular systems. We validate one of these (found in the 3' UTR of TGME49_261720) using a reporter cell line. We show that the presence of the stem-loop-containing UTR is sufficient to confer accumulation at the transcript and protein levels under low iron. This response is dose and time-dependent and is specific for iron. The accumulation of transcript is likely driven by an increased reporter mRNA stability under low iron. Interestingly, we find iron-mediated changes in mRNA stability in around 400 genes. To examine the potential mechanism of this stability, we tested aconitase interaction with mRNA in low iron and found 43 enriched transcripts, but no specific interaction with our reporter UTR. However, the endogenous UTR led to maintenance of protein levels and increased survival of the parasite under low iron. Our data demonstrate the existence of iron-mediated post-transcriptional regulation in Toxoplasma for the first time; and suggests iron-mediated regulation may be important to the parasite in low iron environments.

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Publication Details

Journal
PLoS Pathogens
Published
2025-02-03
DOI
https://doi.org/10.1371/journal.ppat.1012857
Citations
9
Primary Topic
Toxoplasma gondii Research Studies
Type
article
Field-Weighted Citation Impact
18.43

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article

Iron-mediated post-transcriptional regulation in Toxoplasma gondii

Megan A. Sloan, Dana Aghabi, Adam Scott, Clare R. Harding et al.
9 citations
PLoS Pathogens
Toxoplasma gondii Research Studies
18.43
article

Iron-mediated post-transcriptional regulation in Toxoplasma gondii

Megan A. Sloan, Dana Aghabi, Adam Scott, Clare R. Harding, Lucia Mrvova
article en
9 citations

Abstract

Iron is required to support almost all life; however, levels must be carefully regulated to maintain homeostasis. Although the obligate parasite Toxoplasma gondii requires iron, how it responds upon iron limitation has not been investigated. Here, we show that iron depletion triggers significant transcriptional changes in the parasite, including in iron-dependent pathways. We find that a subset of T. gondii transcripts contain stem-loop structures, which have been associated with post-transcriptional iron-mediated regulation in other cellular systems. We validate one of these (found in the 3' UTR of TGME49_261720) using a reporter cell line. We show that the presence of the stem-loop-containing UTR is sufficient to confer accumulation at the transcript and protein levels under low iron. This response is dose and time-dependent and is specific for iron. The accumulation of transcript is likely driven by an increased reporter mRNA stability under low iron. Interestingly, we find iron-mediated changes in mRNA stability in around 400 genes. To examine the potential mechanism of this stability, we tested aconitase interaction with mRNA in low iron and found 43 enriched transcripts, but no specific interaction with our reporter UTR. However, the endogenous UTR led to maintenance of protein levels and increased survival of the parasite under low iron. Our data demonstrate the existence of iron-mediated post-transcriptional regulation in Toxoplasma for the first time; and suggests iron-mediated regulation may be important to the parasite in low iron environments.

PLoS PathogensVol. 21(2)
University of Glasgow (GB)
Wellcome Trust
Openalex Percentile: Top 0%
Toxoplasma gondii Research Studies
18.43
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Iron-mediated post-transcriptional regulation in Toxoplasma gondii — Megan A. Sloan, Dana Aghabi, et al. · PLoS Pathogens (2025) | TGRS Research Map | TGRS