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小鼠高亲和力FcγRI编码基因的结构与定位以及人FcγRI基因的染色体定位

Structure and mapping of the gene encoding mouse high affinity Fc gamma RI and chromosomal location of the human Fc gamma RI gene.

作者信息

Osman N, Kozak C A, McKenzie I F, Hogarth P M

机构信息

Austin Research Institute, Austin Hospital, Heidelberg, Australia.

出版信息

J Immunol. 1992 Mar 1;148(5):1570-5.

PMID:1531670
Abstract

We describe the isolation and characterization of the gene encoding the mouse high affinity Fc receptor Fc gamma RI. Using a mouse cDNA Fc gamma RI probe four unique overlapping genomic clones were isolated and were found to encode the entire 9 kb of the mouse Fc gamma RI gene. Sequence analysis of the gene showed that six exons account for the entire Fc gamma RI cDNA sequences including the 5'- and 3'-untranslated sequences. The first and second exons encode the signal peptide; exons 3, 4, and 5 encode the extracellular Ig binding domains; and exon 6 encodes the transmembrane domain, the cytoplasmic region, and the entire 3'-untranslated sequence. This exon pattern is similar to Fc gamma RIII and Fc epsilon RI but differs from the related Fc gamma RII gene which contains 10 exons and encodes the b1 and b2 Fc gamma RII. Southern blot analysis had shown that the mouse Fc gamma RI gene is a single copy gene with no RFLP in inbred strains of mice, but analysis of an intersubspecies backcross of mice showed that unlike other mouse FcR genes which are on mouse chromosome 1 the locus encoding Fc gamma RI, termed Fcg1, is located on chromosome 3. Interestingly, the Fcg1 locus is located near the end of a region with known linkage homology to human chromosome 1. Analysis of human x rodent somatic cell hybrid cell lines indicates that the human FCG1 locus encoding the human Fc gamma RI maps to chromosome I and therefore possibly linked to other FcR genes on this chromosome. These results suggest that the linkage relationships among these genes in the human genome are not preserved in the mouse.

摘要

我们描述了编码小鼠高亲和力Fc受体FcγRI的基因的分离与鉴定。使用小鼠cDNA FcγRI探针分离出四个独特的重叠基因组克隆,发现它们编码整个9 kb的小鼠FcγRI基因。该基因的序列分析表明,六个外显子构成了包括5'和3'非翻译序列在内的整个FcγRI cDNA序列。第一和第二个外显子编码信号肽;外显子3、4和5编码细胞外Ig结合结构域;外显子6编码跨膜结构域、细胞质区域以及整个3'非翻译序列。这种外显子模式与FcγRIII和FcεRI相似,但与相关的FcγRII基因不同,后者包含10个外显子,编码b1和b2 FcγRII。Southern印迹分析表明,小鼠FcγRI基因是单拷贝基因,在近交系小鼠中无RFLP,但对小鼠亚种间回交的分析表明,与位于小鼠1号染色体上的其他小鼠FcR基因不同,编码FcγRI的基因座(称为Fcg1)位于3号染色体上。有趣的是,Fcg1基因座位于与人类1号染色体具有已知连锁同源性的区域末端附近。对人-啮齿类体细胞杂交细胞系的分析表明,编码人FcγRI的人FCG1基因座定位于1号染色体,因此可能与该染色体上的其他FcR基因连锁。这些结果表明,这些基因在人类基因组中的连锁关系在小鼠中未得到保留。

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