性饮食改变了KMT2D卡布基综合征中的核糖体蛋白失调
Erica Tsang1, Velda X Han2, Chloe Flutter3
1Kids Neuroscience Centre, The Children's Hospital at Westmead, Faculty of Medicine and Health, University of Sydney, NSW, Australia; The Children's Hospital at Westmead Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
EBioMedicine
|May 20, 2024
概括
性饮食可以通过表观遗传变化纠正核糖体和免疫失调来改善卡布基综合征. 这种饮食通过通过体影响基因表达,对神经发育障碍有很大的希望.
科学领域:
- 遗传学 是一个遗传学.
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 神经科学是一个神经科学.
背景情况:
- 卡布基综合征 (KS) 是一种由KMT2D突变引起的遗传疾病,影响染色质结构和基因表达.
- 来自性饮食的类素作为激素脱乙酶抑制剂,可能抵消KS相关的表观遗传变化.
- 临床前研究表明,性饮食可以通过子表观遗传学在KS模型中拯救神经发生.
研究的目的:
- 调查卡布基综合征背后的分子机制.
- 探索基因饮食对KS分子路径和临床结果的影响.
主要方法:
- 采用单细胞RNA测序和基于质谱的蛋白质组学.
- 分析了KS (n=4) 和对照 (n=4) 个体的分子概况.
主要成果:
- 在KS中KMT2D突变与RNA和蛋白质水平上的核糖体蛋白质失调有关.
- 蛋白质组学揭示了KS的免疫失调和补偿性组织蛋白结合蛋白.
- 一名KS患者在基因饮食中表现出更好的认知能力和更正的转录组失调.
结论:
- 在KS中氨酸甲基转移酶缺乏与核糖体和免疫系统功能障碍有关.
- 食可以诱导表观遗传变化,改善KS的临床结果.
- 将多学科数据与临床发现相结合,对于理解神经发育障碍和治疗效果至关重要.
相关概念视频
Inborn Errors of Metabolism
155
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
155
Overview of Protein Metabolism
1.0K
Proteins are broken down into amino acids during digestion. Unlike fats and carbohydrates, which are stored for later use, proteins are not. Instead, amino acids are either used to produce ATP through oxidation or contribute to the creation of new proteins for the growth and repair of the body. Any surplus amino acids from the diet are converted into glucose or triglycerides rather than excreted.
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
1.0K
Translation
141.9K
Lesson: Translation
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of...
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of...
141.9K
Covalently Linked Protein Regulators
6.8K
Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
These groups modify specific amino acids in a protein....
6.8K
Protein Modifications in the RER
5.1K
Modification of secretory and transmembrane proteins entering the rough ER begins in the ER lumen. These modifications aid in protein folding and stabilize the acquired tertiary structure. Protein modifications in the rough ER co-occur at different stages of protein folding.
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal...
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal...
5.1K
PI3K/mTOR/AKT Signaling Pathway
3.5K
The mammalian target of rapamycin (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast, mTORC2 consists of a...
3.5K


