ABSTRACT
Disorders of iron metabolism account for some of the most common human diseases. Cellular iron homeostasis is maintained by iron regulatory proteins (IRP)-1 and 2 through their binding to cis-regulatory iron-responsive elements (IREs) in target mRNAs. Mouse models with IRP deficiency have yielded valuable insights into iron biology, but the physiological consequences of gain of IRP function in mammalian organisms have remained unexplored. Here, we report the generation of a mouse line allowing conditional expression of a constitutively active IRP1 mutant (IRP1) using Cre/Lox technology. Systemic activation of the IRP1 transgene from the Rosa26 locus yields viable animals with gain of IRE-binding activity in all the organs analyzed. IRP1 activation alters the expression of IRP target genes and is accompanied by iron loading in the same organs. Furthermore, mice display macrocytic erythropenia with decreased hematocrit and hemoglobin levels as well as impaired erythroid differentiation. Thus, inappropriately high IRP1 activity causes disturbed body iron distribution and erythropoiesis. This new mouse model further highlights the importance of appropriate IRP regulation in central organs of iron metabolism. Moreover, it opens novel avenues to study diseases associated with abnormally high IRP1 activity, such as Parkinson's disease or Friedreich's ataxia.
Subject(s)
Iron Regulatory Protein 1/genetics , Iron Regulatory Protein 1/metabolism , Iron/metabolism , Anemia, Macrocytic/metabolism , Animals , Duodenum/metabolism , Erythropoiesis/physiology , Female , Iron-Regulatory Proteins/metabolism , Liver/metabolism , Male , Mice , Mice, Transgenic , Spleen/metabolismABSTRACT
BACKGROUND: Mutations of the 3' end mRNA-processing signal of the prothrombin (F2) gene have been reported to cause elevated F2 plasma concentrations, thrombosis, and complications of pregnancy. Whereas the common F2 20210*A mutation is almost exclusively found in Caucasians, the F2 20209*T mutation has been reported in Afro-Americans and Afro-Caribbeans only. PATIENTS AND METHODS: Using LightCycler technology, three unrelated Jewish-Moroccan patients tested for obstetric complications were found to be carriers of the F2 20209*T allele. A detailed molecular analysis was performed to identify the functional impact of this mutation. RESULTS: We report three unrelated women of Jewish-Moroccan origin with a F2 20209*T mutation and fetal loss or infertility. The functional analysis revealed that the F2 20209*T mutation stimulates 3' end processing and up-regulates prothrombin protein expression as assessed by a highly sensitive luminescence-based reporter system. CONCLUSIONS: This is the first report of 20209*T in Caucasians, and functional analysis demonstrates that F2 20209*T falls into a general category of mutations of the F2 gene, which may possibly contribute to thrombophilia and complications of pregnancy by interfering with a tightly balanced architecture of non-canonical F2 3' end formation signals.
Subject(s)
Cytosine/chemistry , Jews , Mutation , Prothrombin/genetics , Thymine/chemistry , White People , Adult , Aged , Base Sequence , DNA Primers , Female , Humans , Male , Morocco/ethnology , RNA Processing, Post-Transcriptional , RNA, Messenger/genetics , RNA, Messenger/metabolismABSTRACT
BACKGROUND: Iron regulatory protein 1 (IRP1), a post-transcriptional regulator of iron metabolism, is activated in the duodenum of iron-deficient animals, which is associated with increased iron absorption. In cell cultures IRP1 was also activated by iron-independent signals, such as H(2)O(2). Here we investigate whether luminal perfusion of rat duodenum with H(2)O(2) activates duodenal IRP1 and modulates duodenal iron absorption. METHODS: Duodena from iron-adequate Sprague-Dawley rats were luminally perfused with H(2)O(2). Iron regulatory protein-1 activity was determined in duodenal mucosa or in villus and crypt preparations by an electrophoretic mobility shift assay. Duodenal (59)Fe absorption was measured in isolated, perfused duodenal segments ex vivo and in ligated loops in vivo. (59)Fe uptake from the blood side was assessed after i.v. injection of (59)Fe-nitrilotriacetic acid. RESULTS: Similar to iron deficiency, the perfusion with 0-50 mM of H(2)O(2) increases duodenal IRP1 activity along the entire crypt villus-axis in a dose-dependent manner. After H(2)O(2) treatment, IRP1 remains activated for 12-24 h in the tips and for 72 h in the crypts. In iron-deficiency, IRP activation correlates with increased (59)Fe absorption. However, the H(2)O(2) treatment fails to stimulate any increase in (59)Fe uptake, without promoting damage of mucosal architecture or impairing glucose and water transport. CONCLUSION: Duodenal (59)Fe uptake is not affected by the H(2)O(2)-mediated activation of IRP1.
Subject(s)
Duodenum/metabolism , Hydrogen Peroxide/pharmacology , Iron Deficiencies , Iron Regulatory Protein 1/metabolism , Absorption/drug effects , Animals , Dose-Response Relationship, Drug , Duodenum/drug effects , Duodenum/pathology , Gastric Lavage/methods , Intestinal Mucosa/drug effects , Intestinal Mucosa/metabolism , Intestinal Mucosa/pathology , Iron/pharmacokinetics , Male , Oxidative Stress/physiology , Perfusion , Rats , Rats, Sprague-Dawley , Stomach/pathologyABSTRACT
Gene expression profiling by DNA microarrays has found wide application in many fields of biomedical research. The protocols for this technique are not yet standardized, and for each given step in microarray analysis a number of different protocols are in use. As a consequence, results obtained in different laboratories can be difficult to compare. Of particular importance in this respect are the methods for the preparation of fluorescent cDNA probes that should quantitatively reflect the abundance of different mRNAs in the two samples to be compared. Here we systematically evaluate and compare five different published and/or commercial principles for the synthesis offluorescently labeled probes for microarray analysis (direct labeling, 77 RNA polymerase amplification, aminoallyl labeling, hapten-antibody enzymatic labeling, and 3-D multi-labeled structures). We show that individual labeling methods can significantly influence the expression pattern obtained in a microarray experiment and discuss the respective benefits and limitations of each method.
Subject(s)
DNA Probes/chemical synthesis , Fluorescent Dyes/chemical synthesis , Gene Expression Profiling/methods , Oligonucleotide Array Sequence Analysis/methods , DNA, Complementary/chemistry , HeLa Cells/physiology , Humans , Iron Deficiencies , Reproducibility of Results , Sensitivity and Specificity , Staining and Labeling/methodsABSTRACT
The first step in intestinal iron absorption is mediated by the H(+)-coupled Fe(2+) transporter called divalent cation transporter 1/divalent metal ion transporter 1 (DCT1/DMT1) (also known as natural resistance-associated macrophage protein 2). DCT1/DMT1 mRNA levels in the duodenum strongly increase in response to iron depletion. To study the mechanism of iron-dependent DCT1/DMT1 mRNA regulation, we investigated the endogenous expression of DCT1/DMT1 mRNA in various cell types. We found that only the iron responsive element (IRE)-containing form, which corresponds to one of two splice forms of DCT1/DMT1, is responsive to iron treatment and this responsiveness was cell type specific. We also examined the interaction of the putative 3'-UTR IRE with iron responsive binding proteins (IRP1 and IRP2), and found that IRP1 binds to the DCT1/DMT1-IRE with higher affinity compared to IRP2. This differential binding of IRP1 and IRP2 was also reported for the IREs of transferrin receptors, erythroid 5-aminolevulinate synthase and mitochondrial aconitase. We propose that regulation of DCT1/DMT1 mRNA by iron involves post-transcriptional regulation through the binding of IRP1 to the transporter's IRE, as well as other as yet unknown factors.
Subject(s)
Cation Transport Proteins/genetics , Iron-Binding Proteins , Iron/metabolism , 3' Untranslated Regions , Biological Transport , Caco-2 Cells , Cation Transport Proteins/metabolism , Cations, Divalent/metabolism , Gene Expression Regulation , HeLa Cells , Humans , Iron Regulatory Protein 1 , Iron Regulatory Protein 2 , Iron-Regulatory Proteins , Iron-Sulfur Proteins/metabolism , Nucleic Acid Conformation , Protein Binding , RNA Processing, Post-Transcriptional , RNA-Binding Proteins/metabolism , Regulatory Sequences, Nucleic AcidSubject(s)
Eukaryotic Cells/metabolism , Protein Biosynthesis/physiology , Animals , Artifacts , Binding Sites/physiology , Genes , Genetic Vectors , Humans , Peptide Initiation Factors/metabolism , RNA Processing, Post-Transcriptional/physiology , RNA, Messenger/metabolism , RNA, Transfer/metabolism , RNA, Viral/metabolism , Reproducibility of Results , Research Design , Ribosomes/metabolismABSTRACT
Binding of phosphorothioate-modified antisense oligodeoxynucleotides (AS ODNs) to target mRNAs is commonly thought to mediate RNA degradation or block of translation. Here we demonstrate cleavage of target mRNAs within the AS ODN binding region with subsequent degradation of the 5' but not the 3' cleavage product. Some, if not all, 3' mRNA fragments lacked a 5' cap structure, whereas their poly(A) tail length remained unchanged. Furthermore, they were efficiently translated into N-terminally truncated proteins as demonstrated in three settings: production of shortened hepadnaviral surface proteins, alteration of the subcellular localization of a fluorescent protein, and shift of the transcription factor C/EBPalpha isoform expression levels. Thus, AS treatment may result in the synthesis of N-truncated proteins with biologically relevant effects.
Subject(s)
Oligodeoxyribonucleotides, Antisense/metabolism , Peptide Fragments/metabolism , RNA, Messenger/metabolism , Animals , CCAAT-Enhancer-Binding Protein-alpha/metabolism , Microscopy, Fluorescence , Oligodeoxyribonucleotides, Antisense/chemistry , Peptide Fragments/genetics , Protein Isoforms/metabolism , Protein Precursors/metabolism , RNA Caps/metabolism , RNA, Messenger/genetics , Tumor Cells, CulturedABSTRACT
In the August issue of Developmental Cell, Tay and Richter examine the consequences of eliminating CPEB function in mice. Their studies reveal an important role for this translational regulator at the pachytene stage of germ cell differentiation.
Subject(s)
Germ Cells/physiology , Meiosis/physiology , Protein Biosynthesis , RNA-Binding Proteins/metabolism , Transcription Factors/metabolism , mRNA Cleavage and Polyadenylation Factors , Animals , Cyclin B/genetics , Cyclin B/metabolism , Cyclin B1 , Female , Male , Mice , Mice, Knockout , Proto-Oncogene Proteins c-mos/genetics , Proto-Oncogene Proteins c-mos/metabolism , RNA, Messenger/metabolismSubject(s)
Cell Nucleus/genetics , Protein Biosynthesis , RNA, Messenger/genetics , Cell Fractionation , Cell Nucleus/metabolism , Cytoplasm/metabolism , Fluorescence , HeLa Cells , Humans , Lysine/metabolism , Protein Transport , Proteins/metabolism , RNA, Messenger/metabolism , Transcription, GeneticABSTRACT
The G-->A mutation at position 20210 of the prothrombin or coagulation factor II gene (F2) represents a common genetic risk factor for the occurrence of thromboembolic events. This mutation affects the 3'-terminal nucleotide of the 3' untranslated region (UTR) of the mRNA and causes elevated prothrombin plasma concentrations by an unknown mechanism. Here, we show that the mutation does not affect the amount of pre-mRNA, the site of 3' end cleavage or the length of the poly(A) tail of the mature mRNA. Rather, we demonstrate that the physiological F2 3' end cleavage signal is inefficient and that F2 20210 G-->A represents a gain-of-function mutation, causing increased cleavage site recognition, increased 3' end processing and increased mRNA accumulation and protein synthesis. Enhanced mRNA 3' end formation efficiency emerges as a novel principle causing a genetic disorder and explains the role of the F2 20210 G-->A mutation in the pathogenesis of thrombophilia. This work also illustrates the pathophysiologic importance of quantitatively minor aberrations of RNA metabolism.
Subject(s)
Prothrombin/genetics , RNA Processing, Post-Transcriptional , RNA, Messenger/genetics , RNA, Messenger/metabolism , Thrombophilia/genetics , 3' Untranslated Regions/genetics , 3' Untranslated Regions/metabolism , HeLa Cells , Humans , Immunoblotting , Prothrombin/biosynthesis , RNA Precursors/genetics , RNA Precursors/metabolism , Transcription, Genetic , TransfectionABSTRACT
Picornavirus internal ribosome entry sites (IRESs) are approximately 450 nt. RNA elements that direct internal initiation of translation, such that when placed between the two cistrons of a dicistronic construct, they drive independent translation of the downstream cistron. Consequently they have been widely used for coordinated expression of two or more proteins. All picornavirus IRESs have an AUG triplet at the very 3' end, which is thought to be the actual site of internal ribosome entry. However with some IRESs, such as foot-and-mouth disease virus, and especially poliovirus, the majority of ribosomes do not initiate translation at this putative entry site AUG, but at the next AUG further downstream, which is thought to be accessed by a process of linear ribosome scanning from the entry site. If this is so, then it should be possible to regulate IRES-dependent translation by inserting an iron responsive element (IRE) between the putative entry site AUG and the main functional initiation site. This should make IRES-dependent translation sensitive to the concentration of iron regulatory protein (IRP), the protein that specifically binds to the IRE. This has been attempted with both the foot-and-mouth disease virus and poliovirus IRESs, and was successful in so far as an inhibition specifically of IRES-dependent translation was observed that was strictly dependent on both the presence of IRP and of a functional IRE motif inserted in the sense orientation. However, the range over which expression could be varied was rather limited (three- to fourfold maximum), because some IRES-dependent translation remained completely refractory to inhibition by even very high IRP concentrations. In contrast, with a cap-proximal IRE in the 5' untranslated region of an mRNA translated by the scanning mechanism, addition of sufficient IRP results in complete inhibition. These results support the model of IRES-promoted ribosome entry at an upstream site followed by strictly linear scanning to the main functional initiation site for the majority of internal initiation events, but imply that some ribosomes must access the functional initiation site by another route, possibly a nonlinear shunting-like mechanism.
Subject(s)
Iron-Sulfur Proteins/metabolism , Models, Genetic , Peptide Chain Initiation, Translational , Picornaviridae/genetics , RNA, Viral , RNA-Binding Proteins/metabolism , Ribosomes/metabolism , Aphthovirus/genetics , Base Sequence , HeLa Cells , Humans , Iron/metabolism , Iron-Regulatory Proteins , Molecular Sequence Data , Nucleic Acid Conformation , RNA, Viral/chemistry , RNA, Viral/metabolism , Response ElementsABSTRACT
The expression of several proteins with critical functions in iron metabolism is regulated post-transcriptionally by the binding of iron regulatory proteins, IRP1 and IRP2, to mRNA iron responsive elements (IREs). In iron-deficient tissues and cultured cells, both IRP1 and IRP2 are activated for high affinity IRE binding. Previous work showed that IRP1 is also activated when cultured cells are exposed to H(2)O(2). The well established role of iron and H(2)O(2) in tissue injury (based on Fenton chemistry) suggests that this response may have important pathophysiological implications. This is particularly relevant in inflammation, where cytotoxic immune cells release large amounts of reactive oxygen species. Here, we describe a rat liver perfusion model to study IRP1 activation under H(2)O(2) generation conditions that mimic a physiological inflammatory response, using steady-state concentrations of H(2)O(2) produced by a glucose/ glucose oxidase/catalase system. We show first that stimulated neutrophils are able to increase serum levels of H(2)O(2) by a factor of 10, even in the presence of H(2)O(2)-degrading erythrocytes. We further show that perfusion of rat liver with glucose oxidase leads to a rapid activation of IRE binding activity in the intact organ. Mobility shift assays with liver extracts and IRP1 or IRP2-specific probes indicate that only IRP1 responds to H(2)O(2). Our study demonstrates a principal existence of iron regulation by oxidative stress at the intact organ level. It also provides a link between iron metabolism and the inflammatory response, as H(2)O(2) is a major product of the oxidative burst of neutrophils and macrophages.
Subject(s)
Iron-Sulfur Proteins/metabolism , Liver/metabolism , Oxidative Stress , RNA-Binding Proteins/metabolism , Animals , Iron Regulatory Protein 1 , Iron Regulatory Protein 2 , Iron-Regulatory Proteins , Neutrophil Activation , Neutrophils/metabolism , Rats , Respiratory BurstABSTRACT
Heterogeneous nuclear ribonucleoprotein K (hnRNP-K) is one of a family of 20 proteins that are involved in transcription and post-transcriptional messenger RNA metabolism. The mechanisms that underlie regulation of hnRNP-K activities remain largely unknown. Here we show that cytoplasmic accumulation of hnRNP-K is phosphorylation-dependent. Mitogen-activated protein kinase/extracellular-signal-regulated kinase (MAPK/ERK) efficiently phosphorylates hnRNP-K both in vitro and in vivo at serines 284 and 353. Serum stimulation or constitutive activation of ERK kinase (MEK1) results in phosphorylation and cytoplasmic accumulation of hnRNP-K. Mutation at ERK phosphoacceptor sites in hnRNP-K abolishes the ability to accumulate in the cytoplasm and renders the protein incapable of regulating translation of mRNAs that have a differentiation-control element (DICE) in the 3' untranslated region (UTR). Similarly, treatment with a pharmacological inhibitor of the ERK pathway abolishes cytoplasmic accumulation of hnRNP-K and attenuates inhibition of mRNA translation. Our results establish the role of MAPK/ERK in phosphorylation-dependent cellular localization of hnRNP-K, which is required for its ability to silence mRNA translation.
Subject(s)
Mitogen-Activated Protein Kinases/metabolism , Protein Biosynthesis , Ribonucleoproteins/metabolism , Arachidonate 15-Lipoxygenase/genetics , Blotting, Western , Cell Line , Cells, Cultured , Enzyme Inhibitors/pharmacology , Flavonoids/pharmacology , Genes, Reporter/genetics , Heterogeneous-Nuclear Ribonucleoprotein K , Heterogeneous-Nuclear Ribonucleoproteins , Humans , Microscopy, Fluorescence , Mitogen-Activated Protein Kinases/genetics , Phosphorylation , RNA, Messenger/genetics , RNA, Messenger/metabolism , Recombinant Fusion Proteins/metabolism , Regulatory Sequences, Nucleic Acid/genetics , TransfectionABSTRACT
The cap-binding complex elF4F is involved in ribosome recruitment during the initiation phase of translation and is composed of three subunits: elF4E, -4G, and -4A. The m7GpppN cap-binding subunit eIF4E binds the N-terminal region of eIF4G, which in turn contacts eIF4A through its central and C-terminal regions. We have previously shown, through a tethered-function approach in transfected HeLa cells, that the binding of eIF4G to an mRNA is sufficient to drive productive translation (De Gregorio et al., EMBO J, 1999, 18:4865-4874). Here we exploit this approach to assess which of the other subunits of elF4F can exert this function. eIF4AI or mutant forms of eIF4E were fused to the RNA-binding domain of the lambda phage antiterminator protein N to generate the chimeric proteins lambda4A, lambda4E-102 (abolished cap binding), and lambda4E-73-102 (impaired binding to both, the cap and eIF4G). The fusion proteins were directed to a bicistronic reporter mRNA by means of interaction with a specific lambda-N binding site (boxB) in the intercistronic space. We show that lambda4E-102, but neither the double mutant lambda4E-73-102 nor lambda4A, suffices to promote translation of the downstream gene in this assay. Coimmunoprecipitation analyses confirmed that all lambda-fusion proteins are capable of interacting with the appropriate endogenous eIF4F subunits. These results reveal that eIF4E, as well as eIF4G, can drive ribosome recruitment independent of a physical link to the cap structure. In spite of its interaction with endogenous eIF4G, lambda4A does not display this property. eIF4A thus appears to supply an essential auxiliary function to eIF4F that may require its ability to cycle into and out of this complex.
Subject(s)
Peptide Initiation Factors/chemistry , Peptide Initiation Factors/metabolism , RNA Caps/metabolism , Ribosomes/metabolism , Amino Acid Sequence , Chloramphenicol O-Acetyltransferase/genetics , Cloning, Molecular , Eukaryotic Initiation Factor-4E , Genes, Reporter , HeLa Cells , Humans , Kinetics , Luciferases/genetics , Molecular Sequence Data , Protein Biosynthesis , Protein Subunits , RNA Caps/chemistry , Recombinant Proteins/metabolism , Transfection , beta-Galactosidase/geneticsABSTRACT
15-lipoxygenase (LOX) expression is translationally silenced in early erythroid precursor cells by a specific mRNA-protein complex formed between the differentiation control element in the 3' untranslated region (UTR) and hnRNPs K and E1. The 3'UTR regulatory complex prevents translation initiation by an unknown mechanism. We demonstrate that the 40S ribosomal subunit can be recruited and scan to the translation initiation codon even when the silencing complex is bound to the 3'UTR. However, the joining of the 60S ribosomal subunit at the AUG codon to form a translation competent 80S ribosome is inhibited, unless initiation is mediated by the IGR-IRES of the cricket paralysis virus. These findings identify the critical step at which LOX mRNA translation is controlled and reveal that 60S subunit joining can be specifically regulated.
Subject(s)
3' Untranslated Regions/genetics , Arachidonate 15-Lipoxygenase/genetics , Capsid Proteins , Gene Silencing , Protein Biosynthesis , RNA, Messenger/metabolism , Reticulocytes/metabolism , Ribosomes/metabolism , 3' Untranslated Regions/metabolism , Animals , Arachidonate 15-Lipoxygenase/metabolism , Capsid/genetics , Capsid/metabolism , Cell-Free System , Cloning, Molecular , Genes, Reporter , In Vitro Techniques , Macromolecular Substances , Models, Biological , Models, Genetic , RNA, Heterogeneous Nuclear/genetics , RNA, Heterogeneous Nuclear/metabolism , RNA, Messenger/genetics , Rabbits , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Ribonucleoproteins/genetics , Ribonucleoproteins/metabolism , Ribosomal Proteins/genetics , Ribosomal Proteins/metabolismABSTRACT
Premature translation termination codons are common causes of genetic disorders. mRNAs with such mutations are degraded by a surveillance mechanism termed nonsense-mediated decay (NMD), which represents a phylogenetically widely conserved post-transcriptional mechanism for the quality control of gene expression. How NMD-competent mRNPs are formed and specified remains a central question. Here, we have used human beta-globin mRNA as a model system to address the role of splicing and polyadenylation for human NMD. We show that (i) splicing is an indispensable component of the human beta-globin NMD pathway, which cannot be compensated for by exonic beta-globin 'failsafe' sequences; (ii) the spatial requirements of human beta-globin NMD, as signified by the maximal distance of the nonsense mutation to the final exon-exon junction, are less constrained than in yeast; and (iii) non-polyadenylated mRNAs with a histone 3' end are NMD competent. Thus, the formation of NMD-competent mRNP particles critically depends on splicing but does not require the presence of a poly(A) tail.
Subject(s)
Globins/genetics , RNA Splicing/genetics , Ribonucleoproteins/genetics , Ribonucleoproteins/metabolism , Base Sequence , Codon, Nonsense/genetics , DNA Primers/genetics , HeLa Cells , Humans , In Vitro Techniques , Mutation , Poly A/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/metabolism , TransfectionSubject(s)
Arachidonate 15-Lipoxygenase/genetics , Gene Expression Regulation , Nuclear Proteins/genetics , Protein Biosynthesis , RNA, Messenger/genetics , Transcription Factors/genetics , 3' Untranslated Regions/genetics , Animals , DNA-Binding Proteins , Drosophila Proteins , Kinetics , Mammals , Repressor Proteins/genetics , Repressor Proteins/metabolism , Reticulocytes/enzymologyABSTRACT
The mRNA cap structure is bound by either the nuclear (CBC) or the cytoplasmic (eIF4F) cap binding complex. Following mRNA export, CBC must be exchanged for eIF4F in the cytoplasm. It is not known how this exchange occurs or how this RNP remodeling event is integrated with mRNA function. Here we report genetic and biochemical evidence that the yeast translation initiation factor eIF4G associates with CBC, and that eIF4E, the eIF4F component that binds both the cap and eIF4G, antagonizes this interaction. Furthermore, we find that CBC can stimulate translation in extracts containing an eIF4G protein deficient for eIF4E binding. These data suggest that eIF4E binding to the eIF4G-CBC complex on newly exported mRNA displaces CBC, and that the first round of translation on mRNA may occur via a different mechanism than subsequent rounds.
Subject(s)
Fungal Proteins/metabolism , Peptide Initiation Factors/metabolism , RNA Caps/metabolism , RNA-Binding Proteins/metabolism , Cell Nucleus/metabolism , Eukaryotic Initiation Factor-4G , Fungal Proteins/genetics , Genes, Fungal , Mutation , Peptide Initiation Factors/genetics , Poly(A)-Binding Proteins , Protein Biosynthesis , RNA Cap-Binding Proteins , RNA, Fungal/metabolism , RNA-Binding Proteins/genetics , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/metabolismSubject(s)
Protein Biosynthesis , Proteins/metabolism , RNA/metabolism , Saccharomyces cerevisiae/genetics , Binding Sites , Cell Culture Techniques , Cell Separation , Cloning, Molecular , Cytoplasm/metabolism , DNA, Complementary/metabolism , Flow Cytometry , Genetic Techniques , Green Fluorescent Proteins , Luminescent Proteins , Models, Genetic , Plasmids/metabolism , Protein Binding , Protein Structure, Tertiary , Proteins/genetics , RNA/genetics , RNA-Binding Proteins/genetics , RNA-Binding Proteins/metabolism , Saccharomyces cerevisiae/metabolismABSTRACT
Iron absorption by the duodenal mucosa is initiated by uptake of ferrous Fe(II) iron across the brush border membrane and culminates in transfer of the metal across the basolateral membrane to the portal vein circulation by an unknown mechanism. We describe here the isolation and characterization of a novel cDNA (Ireg1) encoding a duodenal protein that is localized to the basolateral membrane of polarized epithelial cells. Ireg1 mRNA and protein expression are increased under conditions of increased iron absorption, and the 5' UTR of the Ireg1 mRNA contains a functional iron-responsive element (IRE). IREG1 stimulates iron efflux following expression in Xenopus oocytes. We conclude that IREG1 represents the long-sought duodenal iron export protein and is upregulated in the iron overload disease, hereditary hemochromatosis.