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Porphobilinogen deaminase gene therapy

机译:胆色素原脱氨酶基因治疗

摘要

The present invention relates to nucleotide sequences coding for human porphobilinogen deaminase that are optimised for higher expression in mammalian cells. The invention further relates to DNA constructs comprising such optimised synthetic coding sequences for use in gene therapy of conditions caused by a deficiency in porphobilinogen deaminase, such as acute intermittent porphyria. Accordingly, the present invention relates to a nucleic acid or a nucleic acid construct comprising a nucleotide sequence coding for a human porphobilinogen deaminase, wherein at least 320 of the codons coding for the human porphobilinogen deaminase are identical to the codons in SEQ ID NO: 1 or wherein at least 305 of the codons coding for the human porphobilinogen deaminase are identical to the codons in SEQ ID NO: 3.
机译:本发明涉及编码人卟啉胆碱原脱氨酶的核苷酸序列,其被优化用于在哺乳动物细胞中的更高表达。本发明进一步涉及包含这种优化的合成编码序列的DNA构建体,用于基因治疗胆色素原脱氨酶缺乏引起的疾病,例如急性间歇性卟啉症。因此,本发明涉及一种核酸或核酸构建体,其包含编码人血胆色素原脱氨酶的核苷酸序列,其中至少320个编码人血胆色素原脱氨酶的密码子与SEQ ID NO:1中的密码子相同。或其中至少305个编码人卟啉胆碱原脱氨酶的密码子与SEQ ID NO:3的密码子相同。

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