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人类OX40同源物:ACT35抗原的cDNA结构、表达及染色体定位

The human OX40 homolog: cDNA structure, expression and chromosomal assignment of the ACT35 antigen.

作者信息

Latza U, Dürkop H, Schnittger S, Ringeling J, Eitelbach F, Hummel M, Fonatsch C, Stein H

机构信息

Institute of Pathology, Free University of Berlin, FRG.

出版信息

Eur J Immunol. 1994 Mar;24(3):677-83. doi: 10.1002/eji.1830240329.

Abstract

Tissue distribution and expression on mitogen and virally stimulated lymphocytes render the ACT35 molecule a human lymphocyte activation antigen which as yet could not be clustered. Expression cloning of the ACT35 antigen from a pCDM8 library of the HUT-102 cell line revealed strong homology of the cDNA and its encoded protein sequence with the formerly described rat OX40 antigen. The 1.4-kb nucleotide sequence and the deduced 277-amino acid sequence of the single transmembrane protein were 65% and 63% identical, in human and in rat, respectively. Conservation included one N-linked glycosylation site and one protein kinase C phosphorylation site. When expressed in COS-1 cells, the cDNA presented properties comparable to the native ACT35 antigen and the rat OX40 molecule (relative molecular mass 48,000). Thus, the ACT35 protein corresponds to the hitherto unknown human OX40 antigen and is, therefore, another member of the tumor necrosis factor/nerve growth factor receptor (TNFR/NGFR) family. After applying fluorescence in situ hybridization, the human ACT35/OX40 gene could be mapped to chromosome band 1p36 and is, thus, linked to the genes for TNFR II and CD30.

摘要

ACT35分子在有丝分裂原和病毒刺激的淋巴细胞上的组织分布及表达,使其成为一种尚未能归类的人类淋巴细胞激活抗原。从HUT - 102细胞系的pCDM8文库中对ACT35抗原进行表达克隆,结果显示该cDNA及其编码的蛋白质序列与先前描述的大鼠OX40抗原有很强的同源性。该单跨膜蛋白的1.4kb核苷酸序列和推导的277个氨基酸序列在人和大鼠中分别有65%和63%的同一性。保守区域包括一个N - 连接糖基化位点和一个蛋白激酶C磷酸化位点。当在COS - 1细胞中表达时,该cDNA呈现出与天然ACT35抗原及大鼠OX40分子(相对分子质量48,000)相当的特性。因此,ACT35蛋白对应于迄今未知的人类OX40抗原,所以是肿瘤坏死因子/神经生长因子受体(TNFR/NGFR)家族的另一个成员。应用荧光原位杂交后,人类ACT35/OX40基因可定位于染色体带1p36,因此与TNFR II和CD30的基因相关联。

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