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转基因小鼠唾液腺中的组织特异性表达。

Tissue-specific expression in the salivary glands of transgenic mice.

作者信息

Mikkelsen T R, Brandt J, Larsen H J, Larsen B B, Poulsen K, Ingerslev J, Din N, Hjorth J P

机构信息

Department of Molecular Biology, University of Aarhus, Denmark.

出版信息

Nucleic Acids Res. 1992 May 11;20(9):2249-55. doi: 10.1093/nar/20.9.2249.

DOI:10.1093/nar/20.9.2249
PMID:1594444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC312338/
Abstract

Using a DNA construct, named Lama, derived from the murine parotid secretory protein (PSP) gene, we have obtained salivary gland specific gene expression in transgenic mice. Lama is a PSP minigene and allows analysis of the PSP gene 5' regulatory region by transgenesis. We show here that the regulatory region included in Lama with 4.6 kb of 5' flanking sequence is sufficient to direct expression specifically to the salivary glands. The expression level in the parotid gland is only about one percent of the PSP mRNA level, while that of the sublingual gland is near the PSP mRNA level. This suggests significant differences in the PSP gene regulation in the two glands. In addition, Lama is a secretory expression vector in which cDNAs or genomic fragments can be inserted. We demonstrate that the Lama construct can direct the expression of a heterologous cDNA encoding the C-terminal peptide of human factor VIII to salivary glands and that the corresponding peptide is secreted into saliva.

摘要

利用一种名为Lama的DNA构建体,其源自小鼠腮腺分泌蛋白(PSP)基因,我们在转基因小鼠中实现了唾液腺特异性基因表达。Lama是一个PSP小基因,可通过转基因分析PSP基因的5'调控区。我们在此表明,Lama中包含的具有4.6 kb 5'侧翼序列的调控区足以将表达特异性地导向唾液腺。腮腺中的表达水平仅约为PSP mRNA水平的1%,而舌下腺的表达水平接近PSP mRNA水平。这表明两个腺体中PSP基因调控存在显著差异。此外,Lama是一种分泌表达载体,可插入cDNA或基因组片段。我们证明,Lama构建体可将编码人因子VIII C末端肽的异源cDNA的表达导向唾液腺,且相应肽分泌到唾液中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b96/312338/b8bdfba5a509/nar00083-0052-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b96/312338/03f4d121874f/nar00083-0050-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b96/312338/ea73e949520e/nar00083-0050-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b96/312338/6f7fbc502d9d/nar00083-0051-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b96/312338/b8bdfba5a509/nar00083-0052-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b96/312338/03f4d121874f/nar00083-0050-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b96/312338/ea73e949520e/nar00083-0050-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b96/312338/6f7fbc502d9d/nar00083-0051-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b96/312338/b8bdfba5a509/nar00083-0052-a.jpg

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Purification and characterization of a highly purified human factor VIII consisting of a single type of polypeptide chain.由单一类型多肽链组成的高纯度人凝血因子VIII的纯化与特性分析。
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Improvement of anti-nutritional effect resulting from β-glucanase specific expression in the parotid gland of transgenic pigs.转基因猪腮腺中β-葡聚糖酶特异性表达对抗营养作用的改善
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A systems biology approach identifies a regulatory network in parotid acinar cell terminal differentiation.一种系统生物学方法确定了腮腺腺泡细胞终末分化中的调控网络。
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Expression of the retinoblastoma protein RbAp48 in exocrine glands leads to Sjögren's syndrome-like autoimmune exocrinopathy.视网膜母细胞瘤蛋白RbAp48在外分泌腺中的表达会导致干燥综合征样自身免疫性外分泌病。
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Enzyme linked immunosorbent assay (ELISA) for the measurement of factor VIII coagulant antigen (CAg) using haemophilic antibodies.使用血友病抗体通过酶联免疫吸附测定法(ELISA)测量凝血因子 VIII 凝血抗原(CAg)
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