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人癌表达的细胞表面糖蛋白Trop-2编码基因的克隆。

Cloning of the gene encoding Trop-2, a cell-surface glycoprotein expressed by human carcinomas.

作者信息

Fornaro M, Dell'Arciprete R, Stella M, Bucci C, Nutini M, Capri M G, Alberti S

机构信息

Istituto di Ricerche Farmacologiche Mario Negri--Consorzio Mario Negri Sud, Santa Maria Imbaro, Chieti, Italy.

出版信息

Int J Cancer. 1995 Sep 4;62(5):610-8. doi: 10.1002/ijc.2910620520.

DOI:10.1002/ijc.2910620520
PMID:7665234
Abstract

We have cloned by expression the cDNA encoding Trop-2, a cell-surface glycoprotein expressed by most human carcinomas. Formal proof of the identity of the clone is the hybridization to DNA and RNA from genomic TROP2 transfectants. TROP2 is a single-copy gene in human cells, hybridizes to a single 1.8-kb mRNA from expressing sources and encodes a 35,709 Da type-1 transmembrane protein with a single transmembrane domain. TROP2 is essentially identical to GA733-1. Thus, we have proven that GA733-1, for which a protein product had not been identified, is a functional gene. TROP2 is also homologous to TROP1/KSA/GA733-2, confirming the serological similarities between the 2 molecules. The homology between the Trop-1 and Trop-2 peptides is clustered in 2 extracytoplasmic domains and in the transmembrane/cytoplasmic region. Twelve cysteines and a potential cytoplasmic tyrosine phosphorylation site are also conserved. Trop-1 and Trop-2 are homologous to serum IGF-II-binding proteins and appear as signal transducers. Thus, they likely represent novel cell-surface receptors and may play a role in regulating the growth of carcinoma cells. On the other hand, we have found no evidence for a role of Trop-2 and Trop-1 as homophilic adhesion molecules.

摘要

我们通过表达克隆了编码Trop-2的cDNA,Trop-2是一种在大多数人类癌症中表达的细胞表面糖蛋白。该克隆身份的正式证明是与基因组TROP2转染子的DNA和RNA杂交。TROP2是人类细胞中的单拷贝基因,与来自表达源的单一1.8 kb mRNA杂交,并编码一种具有单个跨膜结构域的35,709 Da 1型跨膜蛋白。TROP2与GA733-1基本相同。因此,我们证明了尚未鉴定出蛋白质产物的GA733-1是一个功能基因。TROP2也与TROP1/KSA/GA733-2同源,证实了这两种分子之间的血清学相似性。Trop-1和Trop-2肽之间的同源性集中在两个胞外结构域以及跨膜/胞质区域。十二个半胱氨酸和一个潜在的胞质酪氨酸磷酸化位点也保守存在。Trop-1和Trop-2与血清IGF-II结合蛋白同源,并表现为信号转导分子。因此,它们可能代表新型细胞表面受体,并可能在调节癌细胞生长中发挥作用。另一方面,我们没有发现Trop-2和Trop-1作为同嗜性粘附分子发挥作用的证据。

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