The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload

Clara Camaschella, Alessandro Campanella, Luigia De Falco, Loredana Boschetto, Roberta Merlini, Laura Silvestri, Sonia Levi, Achille Iolascon

Research output: Contribution to journalArticle

227 Citations (Scopus)

Abstract

Inherited microcytic-hypochromic anemias in rodents and zebrafish suggest the existence of corresponding human disorders. The zebrafish mutant shiraz has severe anemia and is embryonically lethal because of glutaredoxin 5 (GRLX5) deletion, insufficient biogenesis of mitochondrial iron-sulfur (Fe/S) clusters, and deregulated iron-regulatory protein 1 (IRP1) activity. This leads to stabilization of transferrin receptor 1 (TfR) RNA, repression of ferritin, and ALA-synthase 2 (ALAS2) translation with impaired heme synthesis. We report the first case of GLRX5 deficiency in a middle-aged anemic male with iron overload and a low number of ringed sideroblasts. A nemia was worsened by blood transfusions but partially reversed by iron chelation. The patient had a homozygous (c.294A>G) mutation that interferes with intron 1 splicing and drastically reduces GLRX5 RNA. As in shiraz, aconitase and H-ferritin levels were low and TfR level was high in the patient's cells, compatible with increased IRP1 binding. Based on the biochemical and clinical phenotype, we hypothesize that IRP2, less degraded by low heme, contributes to the repression of the erythroblasts ferritin and ALAS2, increasing mitochondrial iron. Iron chelation, redistributing iron to the cytosol, might relieve IRP2 excess, improving heme synthesis and anemia. GLRX5 function is highly conserved, but at variance with zebrafish, its defect in humans leads to anemia and iron overload.

Original languageEnglish
Pages (from-to)1353-1358
Number of pages6
JournalBlood
Volume110
Issue number4
DOIs
Publication statusPublished - Aug 15 2007

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Iron Overload
Zebrafish
Anemia
Iron
Iron Regulatory Protein 1
Heme
Transferrin Receptors
Ferritins
Chelation
Glutaredoxins
RNA
Apoferritins
Aconitate Hydratase
Erythroblasts
Organelle Biogenesis
Sulfur
Protein Binding
Blood Transfusion
Cytosol
Introns

ASJC Scopus subject areas

  • Hematology

Cite this

Camaschella, C., Campanella, A., De Falco, L., Boschetto, L., Merlini, R., Silvestri, L., ... Iolascon, A. (2007). The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload. Blood, 110(4), 1353-1358. https://doi.org/10.1182/blood-2007-02-072520

The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload. / Camaschella, Clara; Campanella, Alessandro; De Falco, Luigia; Boschetto, Loredana; Merlini, Roberta; Silvestri, Laura; Levi, Sonia; Iolascon, Achille.

In: Blood, Vol. 110, No. 4, 15.08.2007, p. 1353-1358.

Research output: Contribution to journalArticle

Camaschella, C, Campanella, A, De Falco, L, Boschetto, L, Merlini, R, Silvestri, L, Levi, S & Iolascon, A 2007, 'The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload', Blood, vol. 110, no. 4, pp. 1353-1358. https://doi.org/10.1182/blood-2007-02-072520
Camaschella, Clara ; Campanella, Alessandro ; De Falco, Luigia ; Boschetto, Loredana ; Merlini, Roberta ; Silvestri, Laura ; Levi, Sonia ; Iolascon, Achille. / The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload. In: Blood. 2007 ; Vol. 110, No. 4. pp. 1353-1358.
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AU - Iolascon, Achille

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