Tandem repeats modify the structure of the canine CD1D gene

被引:4
|
作者
van Beeck, F. A. Looringh [1 ]
Leegwater, P. A. J. [2 ]
Herrmann, T. [3 ]
Broere, F. [1 ]
Rutten, V. P. M. G. [1 ,4 ]
Willemse, T. [1 ,2 ]
Van Rhijn, I. [1 ]
机构
[1] Univ Utrecht, Dept Infect Dis & Immunol, Fac Vet Med, NL-3584 CL Utrecht, Netherlands
[2] Univ Utrecht, Dept Clin Sci Compan Anim, Fac Vet Med, NL-3584 CM Utrecht, Netherlands
[3] Univ Wurzburg, Inst Virol & Immunobiol, D-97078 Wurzburg, Germany
[4] Univ Pretoria, Dept Vet Trop Dis, Fac Vet Sci, ZA-0110 Pretoria, South Africa
关键词
CD1; dog; microsatellite; NKT cells; simple sequence repeat; ANTIGEN PRESENTATION; GUINEA-PIG; RECOGNITION;
D O I
10.1111/age.12002
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Among the CD1 proteins that present lipid antigens to T cells, CD1d is the only one that stimulates a population of T cells with an invariant T-cell receptor known as NKT cells. Sequencing of a 722 nucleotide gap in the dog (Canis lupus familiaris) genome revealed that the canine CD1D gene lacks a sequence homologous to exon 2 of human CD1D, coding for the start codon and signal peptide. Also, the canine CD1D gene contains three different short tandem repeats that disrupt the expected gene structure. Because canine CD1D cDNA lacks sequences homologous to human exon 2 and 3, the functionality of canine CD1d protein may be affected, and this could have consequences for the development and activation of canine NKT cells.
引用
收藏
页码:352 / 355
页数:4
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