由于PMPCB基因中的新型拼接变异导致发育回归和无氧的李氏综合征
Emma Matthews1, Ella F Whittle2, Faraan Khan3
1Atkinson-Morley Neuromuscular Centre, Department of Neurology, St George's University Hospitals NHS Foundation Trust, and Molecular and Clinical Sciences Research Institute, St George's University of London, London, UK. e.matthews@sgul.ac.uk.
这就是PMPCB基因.
科学领域:
- 神经遗传学 神经遗传学
- 分子生物学分子生物学
背景情况:
- 在PMPCB基因中的致病变体很少见,以前描述的只有五个孩子.
- 这些孩子出现了莱氏状综合征,基底质病变,缺氧,并且经常在幼儿时代死亡.
研究的目的:
- 报告PMPCB基因中的第一个拼接位变异.
- 描述一个患有PMPCB基因变异的成年患者的临床表现.
主要方法:
- 一个39岁的个体的临床病例描述.
- 迷你基因试验以确认已识别的变种的功能影响.
主要成果:
- 该研究在一名39岁的患者中发现了PMPCB基因中的新型拼接位变异.
- 这种变异被证实会导致异常拼接和12号外显子跳转.
- 患者在儿童中耳炎后表现出发育回归和无氧.
结论:
- 这是PMPCB基因中首次发现拼接部位变异的报告.
- PMPCB基因变异可以呈现出更广泛的临床谱,并影响到成年人的个体.
- 由于拼接位变异的异常拼接是PMPCB相关疾病的机制.
更多相关视频
08:22A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
Published on: December 1, 2017
08:22A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene
Published on: September 16, 2019
相关概念视频
Alternative RNA Splicing
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...
RNA Splicing
Pleiotropy
Inborn Errors of Metabolism
Genomic Imprinting and Inheritance
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
ATP Synthase: Structure
