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组织蛋白酶C在掌跖角化牙周综合征、青春期前牙周炎和侵袭性牙周炎中的作用。

The role of cathepsin C in Papillon-Lefèvre syndrome, prepubertal periodontitis, and aggressive periodontitis.

作者信息

Hewitt Chelsee, McCormick Derek, Linden Gerry, Turk Dusan, Stern Igor, Wallace Ian, Southern Louise, Zhang Liqun, Howard Rebecca, Bullon Pedro, Wong Melanie, Widmer Richard, Gaffar Khaled Abdul, Awawdeh Lama, Briggs Jim, Yaghmai Reza, Jabs Ethlin W, Hoeger Peter, Bleck Oliver, Rüdiger Stefan G, Petersilka Gregor, Battino Maurizio, Brett Peter, Hattab Faiez, Al-Hamed Mohamed, Sloan Philip, Toomes Carmel, Dixon Mike, James Jacqueline, Read Andrew P, Thakker Nalin

机构信息

Department of Medical Genetics University of Manchester, Manchester, UK.

出版信息

Hum Mutat. 2004 Mar;23(3):222-8. doi: 10.1002/humu.10314.

Abstract

We have previously reported that loss-of-function mutations in the cathepsin C gene (CTSC) result in Papillon-Lefèvre syndrome, an autosomal recessive condition characterized by palmoplantar keratosis and early-onset, severe periodontitis. Others have also reported CTSC mutations in patients with severe prepubertal periodontitis, but without any skin manifestations. The possible role of CTSC variants in more common types of non-mendelian, early-onset, severe periodontitis ("aggressive periodontitis") has not been investigated. In this study, we have investigated the role of CTSC in all three conditions. We demonstrate that PLS is genetically homogeneous and the mutation spectrum that includes three novel mutations (c.386T>A/p.V129E, c.935A>G/p.Q312R, and c.1235A>G/p.Y412C) in 21 PLS families (including eight from our previous study) provides an insight into structure-function relationships of CTSC. Our data also suggest that a complete loss-of-function appears to be necessary for the manifestation of the phenotype, making it unlikely that weak CTSC mutations are a cause of aggressive periodontitis. This was confirmed by analyses of the CTSC activity in 30 subjects with aggressive periodontitis and age-sex matched controls, which demonstrated that there was no significant difference between these two groups (1,728.7 +/- SD 576.8 micro moles/mg/min vs. 1,678.7 +/- SD 527.2 micro moles/mg/min, respectively, p = 0.73). CTSC mutations were detected in only one of two families with prepubertal periodontitis; these did not form a separate functional class with respect to those observed in classical PLS. The affected individuals in the other prepubertal periodontitis family not only lacked CTSC mutations, but in addition did not share the haplotypes at the CTSC locus. These data suggest that prepubertal periodontitis is a genetically heterogeneous disease that, in some families, just represents a partially penetrant PLS.

摘要

我们之前报道过,组织蛋白酶C基因(CTSC)的功能丧失突变会导致帕皮永-勒费弗尔综合征,这是一种常染色体隐性疾病,其特征为掌跖角化病和早发性重度牙周炎。其他人也报道过严重青春期前牙周炎患者存在CTSC突变,但无任何皮肤表现。尚未研究CTSC变异体在更常见的非孟德尔式早发性重度牙周炎(“侵袭性牙周炎”)中的可能作用。在本研究中,我们调查了CTSC在这三种病症中的作用。我们证明帕皮永-勒费弗尔综合征在遗传上具有同质性,其突变谱包括21个帕皮永-勒费弗尔综合征家系(包括我们之前研究中的8个家系)中的三个新突变(c.386T>A/p.V129E、c.935A>G/p.Q312R和c.1235A>G/p.Y412C),这为深入了解CTSC的结构-功能关系提供了线索。我们的数据还表明,功能完全丧失似乎是该表型表现所必需的,这使得弱CTSC突变不太可能是侵袭性牙周炎的病因。对30名侵袭性牙周炎患者和年龄及性别匹配的对照组进行的CTSC活性分析证实了这一点,结果表明两组之间无显著差异(分别为1728.7±标准差576.8微摩尔/毫克/分钟和1678.7±标准差527.2微摩尔/毫克/分钟,p = 0.73)。在两个青春期前牙周炎家系中仅在其中一个家系检测到CTSC突变;就经典帕皮永-勒费弗尔综合征中观察到的突变而言,这些突变并未形成一个单独的功能类别。另一个青春期前牙周炎家系中的患病个体不仅没有CTSC突变,而且在CTSC基因座上也没有共享单倍型。这些数据表明青春期前牙周炎是一种遗传异质性疾病,在一些家系中,它只是部分显性的帕皮永-勒费弗尔综合征。

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