展开蛋白质反应调节器ATF6中的突变会导致听力和视力丧失综合征
Eun-Jin Lee1,2,3, Kyle Kim1,3, Monica Sophia Diaz-Aguilar1,2,3,4
1Departments of Pathology and.
The Journal of clinical investigation
|November 21, 2024
概括
激活转录因子6 (ATF6) 缺乏导致渐进性听力损失和耳毛细胞损伤. 这突出了ATF6的特点.
科学领域:
- 细胞生物学 细胞生物学
- 遗传学 是一个遗传学.
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
背景情况:
- 激活转录因子6 (ATF6) 调节了未折叠的蛋白质反应 (UPR),对ER功能至关重要.
- 功能丧失的ATF6突变会导致黑色,这是一个形光感受器疾病.
- 对ATF6功能障碍对其他组织和疾病的更广泛影响基本上是未知的.
研究的目的:
- 调查ATF6在耳健康和神经感官听力中的作用.
- 探索ATF6相关听力损失背后的细胞和分子机制.
主要方法:
- 研究了具有ATF6疾病等位基因的患者的听力投诉.
- 使用Atf6-/-小鼠来模拟听力缺陷.
- 在Atf6-/-小鼠的尾管上进行了转录组学分析.
主要成果:
- 在患者和Atf6-/-小鼠中发现了渐进的感觉神经听力损失.
- 在受影响的小鼠中观察到无组织的立体和外部毛细胞损失.
- 在Atf6-/-内发现了显著的UPR诱导,特别是通过PERK通路,在Atf6-/-内.
结论:
- ATF6对于保持耳健康和听觉功能至关重要.
- ATF6的失活会导致渐进的神经感官听力损失,可能是影响光受体和毛发细胞的综合征的一部分.
- 细胞内膜网膜压力是耳损伤的关键机制,这表明改变生活方式以减少ER压力可能会使患者受益.
相关概念视频
The Unfolded Protein Response
4.4K
The ER is the hub of protein synthesis in a cell. It has robust systems to quality control protein folding and also for degradation of terminally misfolded proteins. Under normal conditions, a small proportion of misfolded proteins that cannot be salvaged need to be transported to the cytoplasm by the ER-associated degradation or ERAD pathways. However, if the ERAD cannot handle the misfolded proteins, the cell activates the unfolded protein response or UPR to adjust the protein folding...
4.4K
Mutations
80.2K
Overview
80.2K
Translation
141.5K
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...
141.5K
Genetic Lingo
101.1K
Overview
101.1K
Pleiotropy
39.8K
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,...
39.8K
Alternative RNA Splicing
21.0K
Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
21.0K


