ACTN3基因rs1815739多态性在下颌骨形态发生中的作用及影响

IF 2.4 3区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Ashwin Mathew George, Jayaseelan Vijayashree Priyadharsini, Sumathi Felicita, Shantha Sundari, Aravind Kumar Subramanian
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引用次数: 0

摘要

目的:α-肌动素-3 (ACTN3)基因的遗传多态性影响面部骨骼轮廓,α-肌动素蛋白的活性影响咬肌的收缩特性。本研究通过停止密码子(将577RR改变为577XX)检测了ACTN3 rs1815739多态性与下颌形态发生变化之间的关联。材料与方法:将250名受试者分为三组。对照组(第一组)100例骨骼I类错颌畸形患者。实验组(2组)150例骨性ⅱ类错颌伴颌突后畸形患者,根据牙体高度(短牙体高度- 2a组)和(长牙体高度- 2b组)分为两组,每组75例。分析受试者唾液样本,鉴定rs1815739基因型。取组织样本定量研究不同等位基因的mRNA表达。结果:具有危险纯合TT基因型的ACTN3基因多态性仅与短体高相关。高度可变的多态性位点显示了祖先等位基因胞嘧啶(C)被胸腺嘧啶(T)抑制蛋白合成所取代。结论:ACTN3 577XX多态性在德拉威人人群中骨骼ⅱ类错颌和短支高的个体中更为常见。它导致咬肌蛋白表达减少,从而导致矢状面和垂直面尺寸的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of ACTN3 Gene rs1815739 Polymorphism and Its Effects on Mandibular Morphogenesis.

Objectives: Genetic polymorphism of the α-actinin-3 (ACTN3) gene has an influence on the facial skeletal profile, with the activity of the α-actinins protein influencing the contractile properties of the masseteric muscles. This study examines the association between the ACTN3 rs1815739 polymorphism through a Stop Codon (changing 577RR to 577XX) resulting in variations in mandibular morphogenesis.

Materials and methods: Two hundred and fifty subjects were categorised into three groups. The control group (Group 1) comprised 100 patients with skeletal Class I malocclusion. The experimental group (Group 2) had 150 subjects with skeletal Class II malocclusions and a retrognathic mandible, divided into two groups of 75 subjects each based on the ramal heights (short ramal height-Group 2a) and (long ramal height-Group 2b). Saliva samples of the subjects were analysed to identify the genotype of the rs1815739. Tissue samples were taken to quantify the mRNA expression in the different alleles studied.

Results: Polymorphism of the ACTN3 gene with risk homozygous TT genotype was linked only to subjects with short ramal height. The highly variable polymorphic site exhibited a substitution of the ancestral allele cytosine (C) with thymine (T) inhibiting protein synthesis. The mRNA expression was also found to be reduced (p < 0.05) in the short ramal height group.

Conclusion: ACTN3 577XX polymorphism is more common among individuals with skeletal Class II malocclusion and short ramal height in the Dravidian population. It results in decreased protein expression in the masseteric muscle, which contributes to variations in sagittal and vertical facial dimensions.

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来源期刊
Orthodontics & Craniofacial Research
Orthodontics & Craniofacial Research 医学-牙科与口腔外科
CiteScore
5.30
自引率
3.20%
发文量
65
审稿时长
>12 weeks
期刊介绍: Orthodontics & Craniofacial Research - Genes, Growth and Development is published to serve its readers as an international forum for the presentation and critical discussion of issues pertinent to the advancement of the specialty of orthodontics and the evidence-based knowledge of craniofacial growth and development. This forum is based on scientifically supported information, but also includes minority and conflicting opinions. The objective of the journal is to facilitate effective communication between the research community and practicing clinicians. Original papers of high scientific quality that report the findings of clinical trials, clinical epidemiology, and novel therapeutic or diagnostic approaches are appropriate submissions. Similarly, we welcome papers in genetics, developmental biology, syndromology, surgery, speech and hearing, and other biomedical disciplines related to clinical orthodontics and normal and abnormal craniofacial growth and development. In addition to original and basic research, the journal publishes concise reviews, case reports of substantial value, invited essays, letters, and announcements. The journal is published quarterly. The review of submitted papers will be coordinated by the editor and members of the editorial board. It is policy to review manuscripts within 3 to 4 weeks of receipt and to publish within 3 to 6 months of acceptance.
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