Original Research: Generation of non-deletional hereditary persistence of fetal hemoglobin β-globin locus yeast artificial chromosome transgenic mouse models: -175 Black HPFH and -195 Brazilian HPFH
| Autor: | Lesya Novikova, Flavia C. Costa, Halyna Fedosyuk, Kenneth R. Peterson, Matthew P Parker, Robert D. Winefield, Carolina A. Braghini, Renee Neades |
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| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
Hereditary persistence of fetal hemoglobin Locus (genetics) Mice Transgenic Anemia Sickle Cell beta-Globins Biology Real-Time Polymerase Chain Reaction General Biochemistry Genetics and Molecular Biology 03 medical and health sciences Mice hemic and lymphatic diseases Fetal hemoglobin medicine Animals Globin Gene Chromosomes Artificial Yeast Locus control region Fetal Hemoglobin Genetics Genetic heterogeneity Point mutation Articles medicine.disease Flow Cytometry Molecular biology Disease Models Animal 030104 developmental biology Gene Expression Regulation |
| Zdroj: | Experimental biology and medicine (Maywood, N.J.). 241(7) |
| ISSN: | 1535-3699 |
| Popis: | Fetal hemoglobin is a major genetic modifier of the phenotypic heterogeneity in patients with sickle cell disease and certain β-thalassemias. Normal levels of fetal hemoglobin postnatally are approximately 1% of total hemoglobin. Patients who have hereditary persistence of fetal hemoglobin, characterized by elevated synthesis of γ-globin in adulthood, show reduced disease pathophysiology. Hereditary persistence of fetal hemoglobin is caused by β-globin locus deletions (deletional hereditary persistence of fetal hemoglobin) or γ-globin gene promoter point mutations (non-deletional hereditary persistence of fetal hemoglobin). Current research has focused on elucidating the pathways involved in the maintenance/reactivation of γ-globin in adult life. To better understand these pathways, we generated new β-globin locus yeast artificial chromosome transgenic mice bearing the Aγ-globin -175 T > C or -195 C > G hereditary persistence of fetal hemoglobin mutations to model naturally occurring hereditary persistence of fetal hemoglobin. Adult -175 and -195 mutant β-YAC mice displayed a hereditary persistence of fetal hemoglobin phenotype, as measured at the mRNA and protein levels. The molecular basis for these phenotypes was examined by chromatin immunoprecipitation of transcription factor/co-factor binding, including YY1, PAX1, TAL1, LMO2, and LDB1. In -175 HPFH versus wild-type samples, the occupancy of LMO2, TAL1 and LDB1 proteins was enriched in HPFH mice (5.8-fold, 5.2-fold and 2.7-fold, respectively), a result that concurs with a recent study in cell lines showing that these proteins form a complex with GATA-1 to mediate long-range interactions between the locus control region and the Aγ-globin gene. Both hereditary persistence of fetal hemoglobin mutations result in a gain of Aγ-globin activation, in contrast to other hereditary persistence of fetal hemoglobin mutations that result in a loss of repression. The mice provide additional tools to study γ-globin gene expression and may reveal new targets for selectively activating fetal hemoglobin. |
| Databáze: | OpenAIRE |
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