Organisation of the mouse and human 5T4 oncofoetal leucine-rich glycoprotein genes and expression in foetal and adult murine tissues

被引:33
作者
King, KW [1 ]
Sheppard, FC [1 ]
Westwater, C [1 ]
Stern, PL [1 ]
Myers, KA [1 ]
机构
[1] Christie Hosp, Paterson Inst Canc Res, CRC Immunol Grp, Cell & Tumour Biol Sect, Manchester M20 9BX, Lancs, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 1999年 / 1445卷 / 03期
关键词
5T4 oncofetal antigen; leucine rich repeat glycoprotein; human gene; mouse gene; genomic organization; tissue expression;
D O I
10.1016/S0167-4781(99)00055-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human 5T4 oncotrophoblast leucine-rich glycoprotein may contribute to the process of placentation or metastasis by modulating cell adhesion, shape and motility. To understand better the role of 5T4 in development and cancer, the gene structure has been elucidated from both human and mouse genomic clones and mRNA expression has been studied in foetal and adult mouse tissues. The protein coding region is located within the second of two exons, the first exon comprising solely of 5'-untranslated region. Upstream there are no TATA or CAAT boxes, but there are a number of potential Spl binding sites. The murine and human proteins show a homologous domain organisation of the leucine rich repeats (LRR) and associated N- and C-terminal flanking regions, although the hydrophilic sequence which intervenes between the two LRR domains contains six additional amino acids in the mouse. The signal peptide, transmembrane region and cytoplasmic tail sequences are identical as are 6 out of the 7 potential N-linked glycosylation sites. Mouse 5T4 transcripts are abundant in placenta and also highly expressed in embryos while in adult tissues transcripts are restricted to brain and ovary. These patterns of expression and the genomic organisation are discussed in relation to possible function and other recently described LRR containing proteins. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:257 / 270
页数:14
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