Molecular Genetic Analysis and Growth Hormone Treatment in a Three-Generation Chinese Family with Tricho-Rhino-Phalangeal Syndrome I

桑格测序 外显子组测序 身材矮小 生物 遗传学 分子生物学 基因 HEK 293细胞 突变 内分泌学
作者
Yaqin Yan,Shan Huang,Lianjing Huang,Jingyi Zhang,Sujuan Li,Cai Zhang,Xiaoping Luo
出处
期刊:Hormone Research in Paediatrics [S. Karger AG]
卷期号:97 (1): 28-39
标识
DOI:10.1159/000530414
摘要

<b><i>Introduction:</i></b> Tricho-rhino-phalangeal syndrome (TRPS) is a rare genetic disorder characterized by craniofacial and skeletal abnormalities, which is caused by variants in the <i>TRPS1</i> gene. <b><i>Methods:</i></b> Clinical information and follow-up data were collected. Whole-exome sequencing (WES) was performed for variants and validated by Sanger sequencing. Bioinformatic analysis was performed to predict the pathogenicity of the identified variant. Moreover, wild-type and mutated <i>TRPS1</i> vectors were constructed and transfected into human embryonic kidney (HEK) 293T cells. Immunofluorescence experiments were performed to assess the localization and expression of the mutated protein. Western blot analysis and RT-qPCR were used to detect the expression of downstream genes. <b><i>Results:</i></b> The affected family members had typical craniofacial phenotype including sparse lateral eyebrows, pear-shaped nasal tip, and large prominent ears, plus skeletal abnormalities including short stature and brachydactyly. WES and Sanger sequencing identified the <i>TRPS1</i> c.880_882delAAG variant in affected family members. In vitro functional studies showed that the <i>TRPS1</i> variant did not affect the cellular localization and the expression of <i>TRPS1</i>, but the transcriptional repression effect of the <i>TRPS1</i> on the <i>RUNX2</i> and <i>STAT3</i> was disturbed. The proband and his brother have been treated with growth hormone (GH) for 2 years until now, and we have observed the improvement of the linear growth in both. <b><i>Conclusions:</i></b> The variant of c.880_882delAAG in <i>TRPS1</i> was responsible for the pathogenesis of the Chinese family with TRPS I. The treatment of GH could be beneficial for the height outcome in TRPS I patients, and earlier initiation and longer duration of the therapy in prepubertal or early pubertal stage could be associated with better height outcomes.
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