Petit E, Huber M, Rochat A, Bodemer C, Teillac-Hamel D, Müh J P, Revuz J, Barrandon Y, Lathrop M, de Prost Y, Hohl D, Hovnanian A
Wellcome Trust Centre for Human Genetics, University of Oxford, UK.
Eur J Hum Genet. 1997 Jul-Aug;5(4):218-28.
We have investigated 8 patients from 7 unrelated families with lamellar ichthyosis (LI) for defects in the keratinocyte transglutaminase (TGK) gene. We have characterized three novel homozygous mutations and a previously reported splice acceptor site mutation. One patient showed a C-to-T change in the binding site for the transcription factor Sp1 within the promoter region. Another patient had a Gly 143-to-Glu mutation in exon 3 and a third patient, affected with a particular form of LI sparing the four limbs, demonstrated a Val382-to-Met mutation within exon 7. These three patients exhibited drastically reduced transglutaminase activity and an absence of detectable TGK polypeptide, as assessed by immunofluorescence and immunoblotting. Northern blot analysis showed that the Sp1 site mutation was associated with profound reduction of TGK transcript levels whereas normal transcript levels were observed for the two missense mutations. We hypothesize that the Sp1 site mutation impairs transcription of the TGK gene, whereas the two missense mutations induce structural changes leading to protein instability. Linkage to TGK was excluded in another family and no evidence for TGK defect was found in 3 other patients. These results further support the involvement of TGK in some patients with LI. They identify a TGK mutation as a cause for non-generalized LI and further delineate the molecular mechanisms underlying TGK deficiency in LI.
我们对来自7个不相关家族的8例板层状鱼鳞病(LI)患者进行了角质形成细胞转谷氨酰胺酶(TGK)基因突变检测。我们鉴定出3个新的纯合突变和1个先前报道的剪接受体位点突变。1例患者在启动子区域转录因子Sp1的结合位点发生了C到T的改变。另1例患者外显子3发生了Gly 143到Glu的突变,第3例患有特殊形式的LI(四肢未受累)的患者,外显子7出现了Val382到Met的突变。通过免疫荧光和免疫印迹评估,这3例患者的转谷氨酰胺酶活性大幅降低,且未检测到可检测的TGK多肽。Northern印迹分析表明,Sp1位点突变与TGK转录水平的显著降低相关,而两个错义突变的转录水平正常。我们推测,Sp1位点突变损害了TGK基因的转录,而两个错义突变导致结构改变,进而导致蛋白质不稳定。在另一个家族中排除了与TGK的连锁关系,在另外3例患者中未发现TGK缺陷的证据。这些结果进一步支持了TGK与部分LI患者发病有关。它们确定了TGK突变是导致非全身性LI的原因,并进一步阐明了LI中TGK缺乏的分子机制。