与PIK3C2A相关的临床表型和细胞表化与功能性SHH初级乳头缺陷相关
Adella Karam1, Clarisse Delvallée1, Bénédicte Gérard2
1Laboratoire de Génétique médicale, UMR_S INSERM U1112, Institut de Génétique Médicale D'alsace (IGMA), Université de Strasbourg, Strasbourg, France.
Clinical genetics
|June 21, 2025
概括
PIK3C2A基因变异导致影响发育的罕见综合征. 这项研究确定了与白内障和聋相关的新变异,扩大了已知的PIK3C2A相关疾病谱.
科学领域:
- 遗传学 遗传学 是一个
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 酸丁醇-3-酶 (PI3K) 对于细胞信号传递至关重要.
- 一个II类PI3K的PIK3C2A,调节细胞生长,运动和毛功能.
- PIK3C2A变体与眼骨牙综合征 (OCSKD) 有关.
研究的目的:
- 在一个患有新型PIK3C2A相关综合征的家庭中研究PIK3C2A基因.
- 描述这种新呈现的临床和分子特征.
- 了解已识别的PIK3C2A变体的功能后果.
主要方法:
- 三元外体序列测序用于识别遗传变异.
- 患者皮肤纤维细胞的功能测试.
- 分析蛋白质水平,酶活性和细胞表型 (,增殖).
主要成果:
- 确定了两个新型化合物异构性PIK3C2A变体.
- 患者的纤维细胞显示正常的PIK3C2A蛋白水平,但酶活性有缺陷.
- 在患者细胞中观察到皮形成/功能受损和增殖能力下降.
结论:
- 这项研究扩大了PIK3C2A相关疾病的临床和突变谱.
- 这些发现突显了PIK3C2A在视觉和听觉发育中的作用.
- 功能性研究对于了解PIK3C2A变种的致病性至关重要.
相关概念视频
Microtubules in Signaling
1.8K
The primary cilium, made up of microtubules, acts as antennae on the cell surfaces for relaying external stimuli into the cells. These fine hair-like structures are present, generally one per cell. These are non-motile cilia in a 9+0 microtubules arrangement, where the central pair of microtubules are absent. The primary cilia arise from the basal body embedded in the cell membrane. Intraflagellar transport (IFT) carries requisite proteins from the cytoplasm to the cilium because the primary...
1.8K
Hedgehog Signaling Pathway
7.5K
The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
7.5K
Cytoskeletal Linker Proteins - Plakins
2.4K
Plakins are large proteins with binding domains for microtubules, microfilaments, intermediate filaments, and membrane-associated protein complexes at cell junctions. Plakin functions are evolutionarily conserved and are primarily involved in organizing the different components of the cytoskeleton by crosslinking them to each other and connecting them to the cell-matrix and cell adhesion complexes. They are also known to interact with signal transducers, serve as scaffolds for signaling...
2.4K
Pleiotropy
41.2K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
41.2K
Notch Signaling Pathway
4.5K
The Notch signaling pathway is a major intracellular signaling pathway that is highly conserved over a broad spectrum of metazoan species. It stands unique from other intracellular signaling mechanisms in animals because notch protein itself acts as the receptor as well as the primary signaling molecule.
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
4.5K


