首页> 外国专利> AGENT FOR TREATMENT OF HUMAN BODY STATES RELATED TO P4HA1 GENE REDUCED EXPRESSION AND/OR REDUCED QUANTITY OF PROLYL 4-HYDROXYLASE ALPHA 1 PROTEIN ON BASIS OF GENE-THERAPEUTIC SUBSTANCES WITH P4HA1 GENE, METHOD OF MANUFACTURE AND OPERATION

AGENT FOR TREATMENT OF HUMAN BODY STATES RELATED TO P4HA1 GENE REDUCED EXPRESSION AND/OR REDUCED QUANTITY OF PROLYL 4-HYDROXYLASE ALPHA 1 PROTEIN ON BASIS OF GENE-THERAPEUTIC SUBSTANCES WITH P4HA1 GENE, METHOD OF MANUFACTURE AND OPERATION

机译:基于P4HA1基因的基因治疗性物质治疗P4HA1基因减少的人体态的相关药物,脯氨酰4-羟化酶α1蛋白的表达和/或数量减少,其制备方法和操作

摘要

FIELD: biology.;SUBSTANCE: invention relates to molecular biology, biotechnology, genetic engineering and medicine and is a means for treating conditions of the human body associated with a decrease in the expression of the P4HA1 gene and/or a decrease in the amount of protein spilled 4-hydroxylase alpha 1, based on gene therapy substances with the P4HA1 gene, at least one gene therapeutic substance selected from the group of gene therapeutic substances, each representing a genetic construct based on a vector plasmid comprising the cDNA of the P4HA1 gene, with the coding sequence of the protein spilled 4-hydroxylase alpha 1, with deletions 5'- and 3'-non-translated regions, namely the unmodified cDNA gene obtained from the site P4HA1 SEQ ID No: 1, or a modified cDNA of the P4HA1 gene, wherein the modified cDNA of the P4HA1 gene is SEQ ID No: 2, or SEQ ID No: 3, or SEQ ID No: 4, or SEQ ID No: 5, or SEQ ID No: 6, or SEQ ID No: 7, or a combination of these genetic constructs, each of which also contains regulatory elements that provide a high level of expression of the P4HA1 gene in eukaryotic cells.;EFFECT: invention effectively increases the amount of protein spilled 4-hydroxylase alpha 1 in eukaryotic cells and to obtain a highly effective agent for the treatment of human body conditions associated with a decrease in the level of expression of the P4HA1 gene and/or a decrease in the amount of the prolyl 4-hydroxylase alpha 1 protein.;7 cl, 20 dwg, 18 ex
机译:技术领域本发明涉及分子生物学,生物技术,基因工程和医学,并且是用于治疗与P4HA1基因表达减少和/或P4HA1基因表达减少有关的人体疾病的手段。基于具有P4HA1基因的基因治疗物质,至少一种选自基因治疗物质的基因治疗物质的蛋白溢出的4-羟化酶α1,每种基因治疗物质均代表基于包含P4HA1基因cDNA的载体质粒的遗传构建体,具有溢出的4-羟化酶α1蛋白的编码序列,具有5'-和3'-非翻译区的缺失,即从位点P4HA1 SEQ ID No:1获得的未修饰的cDNA基因,或P4HA1基因,其中P4HA1基因的修饰cDNA是SEQ ID No:2或SEQ ID No:3或SEQ ID No:4或SEQ ID No:5或SEQ ID No:6或SEQ ID否:7,或这些遗传结构的组合,每个h还包含调节元件,其在真核细胞中提供高水平的P4HA1基因表达。效果:本发明有效地增加了真核细胞中蛋白溢出的4-羟化酶α1的量,并获得了用于治疗真核细胞的高效药物。与P4HA1基因表达水平降低和/或脯氨酰4-羟化酶α1蛋白含量降低相关的人体疾病; 7 cl,20 dwg,18 ex

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