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|Title:||Regulation of erythroid 5-aminolevulinate synthase expression during erythropoiesis|
|Citation:||International Journal of Biochemistry and Cell Biology, 1999; 31(10):1153-1167|
|Publisher:||PERGAMON-ELSEVIER SCIENCE LTD|
|Abstract:||Erythroid tissue is the major site of heme production in the body. The synthesis of heme and globin chains is coordinated at both the transcriptional and post-transcriptional levels to ensure that virtually no free heme or globin protein accumulates. The key rate-controlling enzyme of the heme biosynthetic pathway is 5-aminolevulinate synthase (ALAS) and an erythroid-specific isoform (ALAS2) is up-regulated during erythropoiesis. Differentiation of embryonic stem cells with a disrupted ALAS2 gene has established that expression of this gene is critical for erythropoiesis and cannot be compensated by expression of the ubiquitous isoform of the enzyme (ALAS1). Interestingly, heme appears to be important for expression of globin and other late erythroid genes and for erythroid cell differentiation although the mechanism of this effect is not clear. Transcriptional control elements that regulate the human gene for ALAS2 have been identified both in the promoter and in intronic enhancer regions. Subsequent translation of the ALAS2 mRNA is dependent on an adequate iron supply. The mechanism by which transcription of the gene for ALAS2 is increased by erythropoietin late in erythropoiesis remains an interesting issue. Erythropoietin action may result in altered levels of critical erythroid transcription factors or modulate the phosphorylation/acetylation status of these factors. Defects in the coding region of the gene for ALAS2 underlie the disease state X-linked sideroblastic anemia. In this review, we focus on the regulation and function of erythroid-specific 5-aminolevulinate synthase during erythropoiesis and its role in the X-linked sideroblastic anemia.|
|Keywords:||Animals; Humans; Anemia, Sideroblastic; Iron; Heme; 5-Aminolevulinate Synthetase; Transcription Factors; Cell Differentiation; Erythropoiesis; Protein Biosynthesis; Gene Expression Regulation, Enzymologic; Introns; Enhancer Elements, Genetic; Erythroid Precursor Cells|
|Appears in Collections:||Biochemistry publications|
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