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推定的癌蛋白DEK是青少年类风湿性关节炎中的一种自身抗原,它是与急性髓性白血病相关的嵌合蛋白的一部分。

The putative oncoprotein DEK, part of a chimera protein associated with acute myeloid leukaemia, is an autoantigen in juvenile rheumatoid arthritis.

作者信息

Sierakowska H, Williams K R, Szer I S, Szer W

机构信息

Department of Biochemistry, New York University School of Medicine 10016.

出版信息

Clin Exp Immunol. 1993 Dec;94(3):435-9. doi: 10.1111/j.1365-2249.1993.tb08214.x.

DOI:10.1111/j.1365-2249.1993.tb08214.x
PMID:8252804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1534440/
Abstract

The 45-kD autoantigen associated with juvenile rheumatoid arthritis (JRA) has been isolated from HeLa cell nuclei and purified about 2500-fold to near homogeneity in a five-step chromatographic procedure. Purification of the antigen was monitored by immunoblot assays using a nearly monospecific anti-45-kD serum from a child with JRA. Tryptic peptide mapping and partial amino acid sequencing of the purified 45-kD antigen demonstrated its identity with the DEK protein. DEK is a 43-kD protein of unknown function expressed by the putative oncogene dek located on chromosome 6. As a result of a (6;9) translocation offociated with a rare subtype of acute myeloid leukaemia a chimeric protein containing most of DEK amino acids at the N-terminus is found in leukaemic cells (von Linden et al., Mol Cell Biol. 1992; 12: 1687-97). The 43-kD DEK was detected by immunoblotting with serum from a patient with JRA in a variety of rat tissues, and was most abundant in the spleen and in bone marrow.

摘要

与青少年类风湿性关节炎(JRA)相关的45-kD自身抗原已从HeLa细胞核中分离出来,并通过五步色谱法纯化了约2500倍,达到近乎纯一的状态。使用来自一名JRA患儿的近乎单特异性的抗45-kD血清,通过免疫印迹分析监测抗原的纯化过程。对纯化的45-kD抗原进行胰蛋白酶肽图谱分析和部分氨基酸测序,结果表明它与DEK蛋白相同。DEK是一种43-kD的蛋白质,功能未知,由位于6号染色体上的假定癌基因dek表达。由于与一种罕见的急性髓性白血病亚型相关的(6;9)易位,在白血病细胞中发现了一种在N端含有大部分DEK氨基酸的嵌合蛋白(冯·林登等人,《分子细胞生物学》。1992年;12:1687 - 97)。用JRA患者的血清通过免疫印迹法在多种大鼠组织中检测到了43-kD的DEK,且在脾脏和骨髓中含量最为丰富。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ce/1534440/19cda568e37d/clinexpimmunol00020-0049-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ce/1534440/6b1625971d30/clinexpimmunol00020-0046-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ce/1534440/864900003dfe/clinexpimmunol00020-0047-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ce/1534440/7f57a4aa92d9/clinexpimmunol00020-0048-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ce/1534440/19cda568e37d/clinexpimmunol00020-0049-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ce/1534440/6b1625971d30/clinexpimmunol00020-0046-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ce/1534440/864900003dfe/clinexpimmunol00020-0047-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ce/1534440/7f57a4aa92d9/clinexpimmunol00020-0048-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ce/1534440/19cda568e37d/clinexpimmunol00020-0049-a.jpg

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本文引用的文献

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J Biol Chem. 1986 Aug 25;261(24):11266-73.
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In vitro replication of duplex circular DNA containing the simian virus 40 DNA origin site.含有猿猴病毒40型DNA起始位点的双链环状DNA的体外复制
Proc Natl Acad Sci U S A. 1985 Sep;82(17):5710-4. doi: 10.1073/pnas.82.17.5710.
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Antibodies to histones H1 and H5 in sera of patients with juvenile rheumatoid arthritis.
阿尔茨海默病中的新型分子机制:DEK在疾病发病机制中的潜在作用。
Front Aging Neurosci. 2022 Oct 6;14:1018180. doi: 10.3389/fnagi.2022.1018180. eCollection 2022.
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In silico gene expression and pathway analysis of DEK in the human brain across the lifespan.在人类大脑的整个生命周期中 DEK 的计算机基因表达和途径分析。
Eur J Neurosci. 2022 Sep;56(6):4720-4743. doi: 10.1111/ejn.15791. Epub 2022 Aug 25.
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Loss of DEK Expression Induces Alzheimer's Disease Phenotypes in Differentiated SH-SY5Y Cells.DEK表达缺失在分化的SH-SY5Y细胞中诱导阿尔茨海默病表型。
Front Mol Neurosci. 2020 Nov 16;13:594319. doi: 10.3389/fnmol.2020.594319. eCollection 2020.
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