Rothenburg Stefan, Haag Friedrich, Koch-Nolte Friedrich, Carter Christine, Graham Margaret, Butcher Geoffrey W
Signal Transduction Group, Institute for Immunology, H23W, Universitäts-Klinikum Eppendorf, Martinistr. 52, 20246 Hamburg, Germany.
Immunogenetics. 2005 Nov;57(10):739-49. doi: 10.1007/s00251-005-0026-9. Epub 2005 Nov 8.
ART2 (RT6) belongs to the family of mono-ADP-ribosyltransferases (ARTs). ART2 is a T-cell differentiation marker expressed by the majority of mature peripheral T cells in the rat. The two known ART2 allotypes display approximately 95% amino acid identity. We sequenced the ART2 coding regions from 18 inbred rat strains and found two additional alleles, termed Art2 ( a2 ) and Art2 ( b2 ). Monoclonal antibody Gy12/61 specifically reacted with Art2 ( a2 ) but not Art2 ( a1 ) lymph node cells. Expression of ART2 allotypes in Jurkat cells confirmed this specificity. A polymerase chain reaction (PCR) assay using restriction fragment length polymorphisms is described, which allows the easy discrimination of Art2 alleles. All four laboratory rat alleles, as well as an additional sequence variant, were found amongst 18 wild rat DNA samples. PCR analysis confirmed the selective presence of a rodent identifier (ID) element in the Art2 ( a ) but not the Art2 ( b ) alleles in all rats studied. Analysis of Art2 ( a1 ) and Art2 ( b2 ) genes showed greater divergence in coding than in non-coding regions. Together with the finding of a high number of non-synonymous mutations leading mostly to non-conservative amino acid substitutions clustered on the side facing away from the cell surface, this suggests that the Art2 polymorphism has been subject to selection.
ART2(RT6)属于单磷酸腺苷核糖基转移酶(ARTs)家族。ART2是一种T细胞分化标志物,由大鼠大多数成熟外周T细胞表达。已知的两种ART2同种异型显示出约95%的氨基酸同一性。我们对18个近交系大鼠品系的ART2编码区进行了测序,发现了另外两个等位基因,分别称为Art2(a2)和Art2(b2)。单克隆抗体Gy12/61与Art2(a2)特异性反应,但不与Art2(a1)淋巴结细胞反应。ART2同种异型在Jurkat细胞中的表达证实了这种特异性。本文描述了一种利用限制性片段长度多态性的聚合酶链反应(PCR)检测方法,该方法能够轻松区分Art2等位基因。在18个野生大鼠DNA样本中发现了所有四个实验室大鼠等位基因以及另一个序列变体。PCR分析证实,在所有研究的大鼠中,啮齿动物识别(ID)元件选择性地存在于Art2(a)等位基因而非Art2(b)等位基因中。对Art2(a1)和Art2(b2)基因的分析表明,编码区的差异大于非编码区。再加上发现大量非同义突变主要导致非保守氨基酸替换聚集在远离细胞表面的一侧,这表明Art2多态性受到了选择。