吲哚变异和基因表达的关联分析确定了 MDM4 是骨骼肌肥大和力量型运动员状态的新基因位点。

IF 2.6 4区 医学 Q2 PHYSIOLOGY Experimental Physiology Pub Date : 2024-07-23 DOI:10.1113/EP091992
Hasan H Kazan, Anıl Kasakolu, Seyrani Koncagul, Mehmet A Ergun, George John, Rinat I Sultanov, Andrey V Zhelankin, Ekaterina A Semenova, Rinat A Yusupov, Nikolay A Kulemin, Andrey K Larin, Edward V Generozov, Celal Bulgay, Ildus I Ahmetov
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引用次数: 0

摘要

插入和缺失(indels)是人类基因组中第二常见的变异类型。然而,关于它们与运动相关表型之间关系的数据却很有限。本研究的目的是检测 18,370 个吲哚变异与力量型运动员身份之间的关联,随后对 357,246 人进行了额外研究。在发现阶段,与对照受试者(P = 7.8 × 10-9)和耐力运动员(P = 0.0012)相比,MDM4 基因 rs35493922 I/D 多态性的 D 等位基因在力量型运动员中比例过高。这些发现在独立的队列中得到了重复,显示与对照组(P = 0.016)和耐力组(P = 0.031)相比,力量型运动员的 D 等位基因频率更高。此外,在英国生物库中,D等位基因与更大的去脂质量呈正相关(P = 0.0013)。MDM4 编码一种抑制 p53 活性的蛋白质,而 p53 可诱导肌肉纤维萎缩。因此,我们发现与耐力运动员相比,MDM4 在力量型运动员外侧肌中的表达量明显更高(P = 0.0009),并且与快速肌纤维的百分比(P = 0.0062)和快速肌纤维所占的相对面积(P = 0.0086)呈正相关。MDM4 基因表达与快肌纤维比例增加之间的关系在另外两个队列中得到了证实。最后,我们发现 MDM4 DD 基因型与外侧肌 MDM4 基因表达增加和快肌纤维横截面积增大有关。总之,MDM4 被认为是肌肉纤维规格和大小的潜在调节因子,其吲哚变体与力量型运动员身份有关。重点:本研究的核心问题是什么?哪些吲哚变异具有功能性并与运动和锻炼相关的特征有关?主要发现及其重要性是什么?在测试的 18,370 个吲哚变异中,发现 MDM4 基因 rs35493922 I/D 多态性是功能性变异(影响基因表达),也是最重要的变异,缺失等位基因与力量型运动员身份、去脂质量和快肌纤维横截面积有关。此外,MDM4 的表达与快速肌纤维的百分比和快速肌纤维所占的相对面积呈正相关。
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Association analysis of indel variants and gene expression identifies MDM4 as a novel locus for skeletal muscle hypertrophy and power athlete status.

Insertions and deletions (indels) are the second most common type of variation in the human genome. However, limited data on their associations with exercise-related phenotypes have been documented. The aim of the present study was to examine the association between 18,370 indel variants and power athlete status, followed by additional studies in 357,246 individuals. In the discovery phase, the D allele of the MDM4 gene rs35493922 I/D polymorphism was over-represented in power athletes compared with control subjects (P = 7.8 × 10-9) and endurance athletes (P = 0.0012). These findings were replicated in independent cohorts, showing a higher D allele frequency in power athletes compared with control subjects (P = 0.016) and endurance athletes (P = 0.031). Furthermore, the D allele was positively associated (P = 0.0013) with greater fat-free mass in the UK Biobank. MDM4 encodes a protein that inhibits the activity of p53, which induces muscle fibre atrophy. Accordingly, we found that MDM4 expression was significantly higher in the vastus lateralis of power athletes compared with endurance athletes (P = 0.0009) and was positively correlated with the percentage of fast-twitch muscle fibres (P = 0.0062) and the relative area occupied by fast-twitch muscle fibres (P = 0.0086). The association between MDM4 gene expression and an increased proportion of fast-twitch muscle fibres was confirmed in two additional cohorts. Finally, we found that the MDM4 DD genotype was associated with increased MDM4 gene expression in vastus lateralis and greater cross-sectional area of fast-twitch muscle fibres. In conclusion, MDM4 is suggested to be a potential regulator of muscle fibre specification and size, with its indel variant being associated with power athlete status. HIGHLIGHTS: What is the central question of this study? Which indel variants are functional and associated with sport- and exercise-related traits? What is the main finding and its importance? Out of 18,370 tested indels, the MDM4 gene rs35493922 I/D polymorphism was found to be the functional variant (affecting gene expression) and the most significant, with the deletion allele showing associations with power athlete status, fat-free mass and cross-sectional area of fast-twitch muscle fibres. Furthermore, the expression of MDM4 was positively correlated with the percentage of fast-twitch muscle fibres and the relative area occupied by fast-twitch muscle fibres.

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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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