Koch-Nolte F, Klein J, Hollmann C, Kühl M, Haag F, Gaskins H R, Leiter E, Thiele H G
Department of Immunology, University Hospital, Hamburg, Germany.
Int Immunol. 1995 May;7(5):883-90. doi: 10.1093/intimm/7.5.883.
Rt6 is a T cell-restricted GPI-anchored membrane protein and a member of the family of mono(ADP-ribosyl)transferases. One of the two murine Rt6 genes is deleted in NZW mice. This finding is reminiscent of the deletion of one of the TCR beta genes in the same mouse strain and it is an intriguing possibility that these gene deletions arose by a common genetic mechanism. The Rt6 locus retained by the NZW mouse (designated Rt6-1) is polymorphic among inbred strains of laboratory mice. The NZW mouse shows several strain-specific restriction fragment length variants in this Rt6 locus and five amino acid substitutions occur in the predicted native Rt6 polypeptide of the NZW mouse relative to the corresponding polypeptides of NZB and BALB/c mice. Whereas transcript levels of the two Rt6 genes appear to be normal in spleen and intestine of NZB mice, the corresponding tissues of NZW mice show reduced levels of transcripts from the Rt6 locus retained in this mouse strain. Moreover, reduced levels of Rt6 mRNA also occur in spleen and intestine of (NZB x NZW)F1 hybrid animals, indicating that F1 animals have inherited a dominant factor from the genetic background of the NZW mouse, resulting in low levels of Rt6 expression. It is conceivable that the alterations in the Rt6 genes of the NZW mouse and/or the factor(s) affecting defective Rt6 expression constitute part of the genetic contribution of the NZW mouse to the autoimmune lupus-like disease in (NZB x NZW)F1 animals.(ABSTRACT TRUNCATED AT 250 WORDS)
Rt6是一种T细胞限制性糖基磷脂酰肌醇锚定膜蛋白,属于单(ADP - 核糖基)转移酶家族。在新西兰白兔(NZW)小鼠中,两个鼠源Rt6基因中的一个发生了缺失。这一发现让人联想到同一小鼠品系中TCRβ基因之一的缺失,而且这些基因缺失可能是由共同的遗传机制引起的,这是一个有趣的可能性。NZW小鼠保留的Rt6基因座(命名为Rt6 - 1)在实验室小鼠的近交系中具有多态性。NZW小鼠在这个Rt6基因座上显示出几种品系特异性的限制性片段长度变体,相对于新西兰黑鼠(NZB)和BALB/c小鼠的相应多肽,NZW小鼠预测的天然Rt6多肽中有五个氨基酸取代。虽然NZB小鼠脾脏和肠道中两个Rt6基因的转录水平似乎正常,但NZW小鼠的相应组织中,该小鼠品系保留的Rt6基因座的转录水平降低。此外,(NZB×NZW)F1杂交动物的脾脏和肠道中Rt6 mRNA水平也降低,这表明F1动物从NZW小鼠的遗传背景中继承了一个显性因子,导致Rt6表达水平较低。可以想象,NZW小鼠Rt6基因的改变和/或影响Rt6表达缺陷的因子构成了NZW小鼠对(NZB×NZW)F1动物自身免疫性狼疮样疾病遗传贡献的一部分。(摘要截断于250字)