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Amelioration of β^(654)-thalassemia in mouse model with the knockdown of aberrantly spliced β-globin mRNA 被引量:1

Amelioration of β^(654)-thalassemia in mouse model with the knockdown of aberrantly spliced β-globin mRNA
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摘要 Large amounts of aberrantly spliced mRNA from the β^654 allele was present in erythroid cells, which might impair the erythropoiesis. A therapeutic strategy for β-thalassemia was explored by knocking down the aberrantly spliced mRNA of β-globin. Lentiviral vector with siRNA fragment targets on the specific portion of β^654-globin aberrantly spliced pre-mRNA was constructed. In HeLa β^654 cells, the siRNA vector could reduce approximately 60% of aberrantly spliced mRNA, which was assessed by RT-PCR and qRT-PCR. Furthermore, a disease model of β^654 thalassemia mice with lentiviral-mediated siRNA was produced by subzonal injection (named Hβi-Hbb^th-4/Hbb^+ transgenic mice). Our results showed that the hemotological parameters were improved in Hβi-Hbb^th-4/Hbb^+ transgenic mice. This study provides a potential way for β^654-thalassemia therapy by knocking down the aberrantly spliced β-globin mRNA, whilst supporting that the aberrantly spliced β-globin mRNA may aggravate the disease. Large amounts of aberrantly spliced mRNA from the β^654 allele was present in erythroid cells, which might impair the erythropoiesis. A therapeutic strategy for β-thalassemia was explored by knocking down the aberrantly spliced mRNA of β-globin. Lentiviral vector with siRNA fragment targets on the specific portion of β^654-globin aberrantly spliced pre-mRNA was constructed. In HeLa β^654 cells, the siRNA vector could reduce approximately 60% of aberrantly spliced mRNA, which was assessed by RT-PCR and qRT-PCR. Furthermore, a disease model of β^654 thalassemia mice with lentiviral-mediated siRNA was produced by subzonal injection (named Hβi-Hbb^th-4/Hbb^+ transgenic mice). Our results showed that the hemotological parameters were improved in Hβi-Hbb^th-4/Hbb^+ transgenic mice. This study provides a potential way for β^654-thalassemia therapy by knocking down the aberrantly spliced β-globin mRNA, whilst supporting that the aberrantly spliced β-globin mRNA may aggravate the disease.
出处 《Journal of Genetics and Genomics》 SCIE CAS CSCD 北大核心 2008年第10期595-601,共7页 遗传学报(英文版)
基金 the National Basic Research Program of China (973 Program) (No 2004CB518806) the National High-tech R&D Program (863 Program) (No 2007AA021206) the National Natural Science Foundation of China (No 30571777) the Chinese National and Shanghai Leading Academic Disci-pline Project (No B204)
关键词 Β-THALASSEMIA small interfering RNA (siRNA) HEMOGLOBIN β-thalassemia small interfering RNA (siRNA) hemoglobin
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