And analysis of the gene encoding the human neonatal Fc receptor

被引:25
作者
Mikulska, JE
Pablo, L
Canel, J
Simister, NE
机构
[1] Polish Acad Sci, Ludwik Hirszfeld Inst Immunol & Expt Therapy, PL-53114 Wroclaw, Poland
[2] Brandeis Univ, Rosenstiel Ctr Basic Biomed Sci, Waltham, MA 02254 USA
[3] Brandeis Univ, WM Keck Inst Cellular Visualizat, Waltham, MA 02254 USA
[4] Brandeis Univ, Dept Biol, Waltham, MA 02254 USA
来源
EUROPEAN JOURNAL OF IMMUNOGENETICS | 2000年 / 27卷 / 04期
关键词
D O I
10.1046/j.1365-2370.2000.00225.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The neonatal Fc receptor, FcRn, is expressed in human placental syncytiotrophoblast, capillary endothelium, intestinal epithelium, and other tissues. By analogy with its role in the mouse, human FcRn is expected to transport maternal IgG to the foetus, and protect circulating IgG from catabolism. The larger subunit of FcRn is homologous to the a chains of the major histocompatibility complex (MHC) class I proteins, but is encoded outside the MHC on chromosome 19. We report the isolation of clones encoding the a chain of human FcRn from chromosome 19-specific libraries. The sequence revealed a similar organization to classical and non-classical MHC, and MHC-related genes. Compared with classical MHC class I genes, the human FcRn a chain gene has expanded by acquiring many repetitive sequences in its introns, including multiple Alu elements in the fourth intron. Primer extension analysis showed that there are two transcription initiation sites in the upstream flanking sequence.
引用
收藏
页码:231 / 240
页数:10
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