解码单基因TGFBR1和TGFBR2突变的临床多样性:对分子机制和次胚性相互作用的见解

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2025-06-19 eCollection Date: 2025-01-01 DOI:10.3389/fcell.2025.1580274
Fadia Abu-Sailik, Nesrin Gariballa, Bassam R Ali
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引用次数: 0

摘要

一些常染色体显性单基因疾病已被证实与转化生长因子-β (TGFβ)信号通路的关键受体TGFBR1和TGFBR2突变有关。尽管这些疾病具有共同的心血管结缔组织表现,但不同的突变表现出显著不同的临床表现,导致不同的疾病,包括Loeys-Dietz综合征Marfan综合征2型(MFS2)和胸主动脉瘤和夹层(TAAD)。此外,一些突变导致Shprintzen-Goldberg综合征,其特征是骨骼畸形和智力残疾,以及心血管受损伤,或血管Ehlers-Danlos综合征(vEDS),与主动脉和内脏自发破裂有关。此外,多发性自愈鳞状上皮瘤(MSSE)是一种罕见的家族性皮肤癌,与这些基因的突变有关。在这些疾病中观察到的这种显着的表型变异性可归因于各种因素,包括突变的性质(包括其在蛋白质中的位置),突变的可变功能影响(亚胚性),信号通路之间复杂相互作用的破坏程度,以及修饰基因或环境因素的影响。除了单倍不全外,tgf - β信号的损伤还可能在其他情况下加剧,例如显性负效应,即突变等位基因通过形成无功能受体低聚物来破坏野生型蛋白的正常活性,阻碍其运输。这篇综述揭示了这些遗传性疾病,强调了与同一基因突变相关的广泛临床表现,其病理生理学和潜在的分子机制。最重要的是,它强调了我们目前理解中的关键差距,同时为未来的研究提出了令人信服的方向。这篇综述还强调了迫切需要解开复杂的基因型-表型相关性,这可能为更精确的诊断和治疗策略铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decoding clinical diversity in monogenic TGFBR1 and TGFBR2 mutations: insights into the interplay of molecular mechanisms and hypomorphicity.

Several autosomal-dominant monogenic disorders have been conclusively associated with mutations in TGFBR1 and TGFBR2, key receptors of the Transforming Growth Factor-β (TGFβ) signaling pathway. Although these disorders share a common cardiovascular connective tissue manifestation, different mutations present with strikingly distinctive clinical presentations leading to distinct disorders, including Loeys-Dietz syndrome Marfan syndrome type 2 (MFS2), and Thoracic Aortic Aneurysms and Dissections (TAAD). In addition, some mutations lead to Shprintzen-Goldberg syndrome which is characterized by skeletal deformities and intellectual disabilities in addition to the cardiovascular involvement, or vascular Ehlers-Danlos Syndrome (vEDS) that is associated with spontaneous rupture of the main arteries and internal organs. Furthermore, Multiple Self-healing Squamous Epithelioma (MSSE), a rare familial skin cancer, is linked to mutations in these genes. This significant phenotypic variability observed in these disorders could be attributed to various factors, ranging from the nature of the mutation including its location within the protein, the variable functional impact of the mutations (hypomorphicity), the level of disruption to the intricate interactions between signaling pathways, and the influence of modifier genes or environmental factors. In addition to haploinsufficiency, the impairment of TGFβ signaling could be exacerbated in other scenarios, such as the dominant-negative effects, in which a mutant allele disrupts the normal activity of the wild-type protein by forming non-functional receptor oligomers, hindering their trafficking. This review sheds light on these hereditary disorders, highlighting the broad spectrum of their clinical presentations associated with mutations in the same gene, their pathophysiology, and underlying molecular mechanisms. Most crucially, it underscores the critical gaps in our current understanding while proposing compelling directions for future research. This review also emphasizes the pressing need to unravel the complex genotype-phenotype correlations, which could pave the way for more precise diagnostic and therapeutic strategies.

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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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