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中国锁骨颅骨发育不全患者中新型RUNX2突变的分析。

Analysis of novel RUNX2 mutations in Chinese patients with cleidocranial dysplasia.

作者信息

Zhang Xianli, Liu Yang, Wang Xiaozhe, Sun Xiangyu, Zhang Chenying, Zheng Shuguo

机构信息

Department of Preventive Dentistry, Peking University School and Hospital of Stomatology, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, Beijing, PR China.

出版信息

PLoS One. 2017 Jul 24;12(7):e0181653. doi: 10.1371/journal.pone.0181653. eCollection 2017.

Abstract

Cleidocranial dysplasia (CCD) is an autosomal dominant inheritable skeletal disorder characterized by cranial dysplasia, clavicle hypoplasia and dental abnormalities. This disease is mainly caused by heterozygous mutations in RUNX2, a gene that encodes an osteoblast-specific transcription factor. In the present study, mutational analyses of RUNX2 gene were performed on four unrelated Chinese patients with CCD. Four different RUNX2 mutations were detected in these patients, including one nonsense mutation (c.199C>T p.Q67X) and three missense mutations (c.338T>G p.L113R, c.557G>C p.R186T and c.673C>T p.R225W). Among them, two mutations (c.199C>T p.Q67X and c.557G>C p.R186T) were novel and the other two had been reported in previous literatures. Except for Q67X mutation located in the Q/A domain, other three mutations were clustered within the highly conserved Runt domain. Green fluorescent protein (GFP) and RUNX2 fusion protein analyses in vitro showed that nuclear accumulation of RUNX2 protein was disturbed by Q67X mutation, while the other two mutations (c.338T>G p.L113R and c.557G>C p.R186T) had no effects on the subcellular distribution of RUNX2. Luciferase reporter assay demonstrated that all the three novel RUNX2 mutations significantly reduced the transactivation activity of RUNX2 on osteocalcin promoter. Our findings enrich the evidence of molecular genetics that the mutations of RUNX2 gene are responsible for CCD.

摘要

锁骨颅骨发育不全症(CCD)是一种常染色体显性遗传性骨骼疾病,其特征为颅骨发育异常、锁骨发育不全和牙齿异常。这种疾病主要由RUNX2基因的杂合突变引起,RUNX2基因编码一种成骨细胞特异性转录因子。在本研究中,对4名无亲缘关系的中国CCD患者进行了RUNX2基因的突变分析。在这些患者中检测到4种不同的RUNX2突变,包括1种无义突变(c.199C>T p.Q67X)和3种错义突变(c.338T>G p.L113R、c.557G>C p.R186T和c.673C>T p.R225W)。其中,2种突变(c.199C>T p.Q67X和c.557G>C p.R186T)是新发现的,另外2种已在先前文献中报道。除了位于Q/A结构域的Q67X突变外,其他3种突变聚集在高度保守的Runt结构域内。体外绿色荧光蛋白(GFP)与RUNX2融合蛋白分析表明,Q67X突变干扰了RUNX2蛋白的核内积累,而其他2种突变(c.338T>G p.L113R和c.557G>C p.R186T)对RUNX2的亚细胞分布没有影响。荧光素酶报告基因检测表明,所有3种新发现的RUNX2突变均显著降低了RUNX2对骨钙素启动子的反式激活活性。我们的研究结果丰富了分子遗传学证据,即RUNX2基因突变是导致CCD的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa5f/5524338/6fa76d47c709/pone.0181653.g001.jpg

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