The influence of genotype on the outcome of gene transfer in beta-thalassemia

基因型对β-地中海贫血基因转移结果的影响

• 批准号: 8441629
• 负责人: STEFANO RIVELLA
• 金额: $ 39.82万
• 依托单位: WEILL MEDICAL COLL OF CORNELL UNIV
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-04-05 至 2015-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8441629
• 关键词: Acute Erythroblastic Leukemia; Address; Affect; Alleles; Alternative Splicing; Animal Model; Ankyrins; Beta Cell; Bypass; Cells; Clinic; Clinical Trials; Code; Data; Disease; Effectiveness; Elements; Erythroid Cells; Erythroid Progenitor Cells; Fetal Hemoglobin; Gene Mutation; Gene Transfer; Genes; Genetic; Genetic Transcription; Genetic Translation; Genomics; Genotype; Globin; Goals; Hemoglobin concentration result; Hereditary Disease; Human; Individual; Introns; Knockout Mice; Knowledge; Lead; Lentivirus Vector; Life; Locus Control Region; Mediating; Messenger RNA; Modality; Modeling; Modification; Molecular; Mus; Mutate; Mutation; Mutation Spectra; Nonsense Codon; Outcome; Parents; Patients; Phenotype; Polyribosomes; Production; Protein Biosynthesis; Proteins; RNA Decay; RNA Splicing; RNA chemical synthesis; Research; Role; Small Nuclear RNA; Subfamily lentivirinae; Testing; Transcript; Transgenic Organisms; Translating; Translations; Viral; alpha Globin; base; beta Globin; beta Thalassemia; cellular transduction; disease phenotype; effective therapy; expression vector; gene therapy; gene transfer vector; improved; lentiviral-mediated; mRNA Decay; mRNA Stability; mutant; novel; promoter; public health relevance; small hairpin RNA; success; therapeutic effectiveness; vector

DESCRIPTION (provided by applicant): Beta-thalassemia is caused by a large spectrum of genetic mutations in the beta-globin gene. These mutations can be classified as beta 0 and beta +, depending upon whether the corresponding allele leads to no or low beta-globin chain synthesis respectively. Depending on the combination of these specific mutations, patients are classified into three principal groups with no, very low or moderately low beta-globin production (beta 0/0, 0/+ and +/+, respectively). Our research, along with that of others, showed that it is possible to rescue beta-thalassemia in mice by lentiviral-mediated transfer of the human beta-globin gene, its promoter, introns and large elements of the locus control region. Based on these studies, clinical trials have been proposed or are underway. However these original studies did not take in consideration the genotypic variability in beta-thalassemia patients. Our goal is to understand whether the outcome of gene transfer is influenced by the mutations in the beta-globin gene. Based on these studies, we will investigate the correlation between genotype and phenotype and generate more efficient gene transfer vectors for the cure of beta-thalassemia. The original studies utilized mice with deleted beta-globin genes. Therefore, these mice do not reproduce the large spectrum of mutations observed in beta-thalassemia patients. Our preliminary data demonstrate that the type of beta-globin gene mutation has a dramatic effect on the expression of the lentiviral mediated wild-type beta-globin. Specifically, we have found that transduction of erythroid progenitor cells (ErPC) from a subset of beta-thalassemic patients (mostly beta 0/0) leads to high beta- globin protein levels proportional to the amount of vector utilized. However, hemoglobin levels in transduced beta +/+ cells increased only slightly or not at all. In beta 0/+ we observed mixed results. We observed a good correlation between the presence of transcripts insensitive to non-sense mediated mRNA decay (NMD) and inhibition of the translation of the transgenic beta-globin mRNA. We propose to better understand the mechanism by which mutant beta-globin mRNAs regulate the expression or translation of normal beta-globin genes, and utilize this knowledge to generate more effective therapies to treat beta-thalassemia. Our preliminary data already suggests one mechanism which may bypass the deleterious effects of the mutated globin gene on a wild-type allele. As opposed to a parent lentiviral vector which does not increase globin expression in beta +/+ cells, modification of this vector with a genomic element from the ankyrin locus completely reversed the phenotype in beta +/+ ErPCs, achieving high level of hemoglobin synthesis. Based on this and other preliminary data, we hypothesize that mutant beta-globin mRNA compete with the normal beta-globin mRNA for translation. Therefore, we have formulated the following aims: Aim 1: To understand the effect of endogenous mutant beta-globin mRNAs on the expression of the transduced normal beta-globin gene. Aim 2: To develop novel expression vectors that restore the ability of the lentiviral mediated beta- globin mRNA to be translated.

描述（由申请人提供）：β-地中海贫血是由β-珠蛋白基因中的大量基因突变引起的。这些突变可以分为β 0和β +，这取决于相应的等位基因是否分别导致没有或低β-珠蛋白链合成。根据这些特定突变的组合，患者被分为三个主要组，没有，非常低或中度低β-珠蛋白生产（β 0/0，0/+和+/+，分别）。我们的研究与其他人的研究沿着表明，通过慢病毒介导的人β-珠蛋白基因、其启动子、内含子和基因座控制区的大元件的转移，有可能挽救小鼠中的β-地中海贫血。基于这些研究，已经提出或正在进行临床试验。然而，这些原始研究没有考虑β-地中海贫血患者的基因型变异性。我们的目标是了解基因转移的结果是否受到β-珠蛋白基因突变的影响。基于这些研究，我们将研究基因型和表型之间的相关性，并产生更有效的基因转移载体用于治疗β-地中海贫血。最初的研究使用了缺失β-珠蛋白基因的小鼠。因此，这些小鼠不会重现在β-地中海贫血患者中观察到的大范围突变。我们的初步数据表明，β-珠蛋白基因突变的类型对慢病毒介导的野生型β-珠蛋白的表达具有显着的影响。具体地，我们已经发现，来自β-地中海贫血患者亚组（主要是β 0/0）的红系祖细胞（ErPC）的转导导致与所用载体的量成比例的高β-珠蛋白水平。然而，转导的β +/+细胞中的血红蛋白水平仅略微增加或根本没有增加。在beta 0/+中，我们观察到混合结果。我们观察到对无义介导的mRNA衰变（NMD）不敏感的转录物的存在与转基因β-珠蛋白mRNA的翻译的抑制之间存在良好的相关性。我们建议更好地了解突变β-珠蛋白mRNA调节正常β-珠蛋白基因表达或翻译的机制，并利用这些知识来产生更有效的治疗β-地中海贫血的疗法。我们的初步数据已经提示了一种机制，它可以绕过突变的珠蛋白基因对野生型等位基因的有害影响。与不增加β +/+细胞中珠蛋白表达的亲本慢病毒载体相反，用来自锚蛋白基因座的基因组元件修饰该载体完全逆转了β +/+ ErPC中的表型，实现了高水平的血红蛋白合成。基于此和其他初步数据，我们假设突变的β-珠蛋白mRNA与正常的β-珠蛋白mRNA竞争翻译。因此，我们制定了以下目标：目标1：了解内源性突变β-珠蛋白mRNA对转导的正常β-珠蛋白基因表达的影响。目的2：开发新的表达载体，恢复慢病毒介导的β-珠蛋白mRNA的翻译能力。