Investigation of the role of the snoRNA U8 in human health and disease
Investigation of the role of the snoRNA U8 in human health and disease
批准号:
MR/V009273/1
负责人:
Yanick Crow
金额:
$77.4万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2021
资助国家:
英国
项目状态:
已结题
起止时间:
2021 至 --
中文摘要
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英文摘要
We want to understand the cause of a rare disease of the brain called leukoencephalopathy with calcifications and cysts (LCC). Although LCC most often affects children, it can actually present at any age, causing problems with seizures, movement and thinking over a period of several years. Patients eventually die of their illness because there is currently no known treatment for LCC.The name LCC comes from the changes that doctors see when they look at the brain scans of affected patients - white matter damage ('leukoencephalopathy'), calcium accumulation (in a particular pattern), and cysts ('holes' in the brain white matter). Because LCC is rare and poorly recognised, and because no diagnostic blood test has been available until recently, affected patients sometimes have a piece of the brain taken out to be looked at under a microscope. Studies of these samples suggest that the problem causing LCC involves the brain blood vessels. We recently discovered changes ('mutations') in a piece of our genetic material (our DNA) called SNORD118 as the cause of LCC. SNORD118 helps our cells to make a different type of genetic material referred to as RNA. The specific piece of RNA mutated in LCC is called U8. We know that U8 is important for producing proteins i.e. chemicals that are crucial for how our cells work. However, how these genetic and chemical changes lead to a problem in the cells of the brain blood vessels is still not known. To improve our understanding of the cause of LCC, we have developed a special zebrafish with a similar genetic problem as is seen in patients affected with LCC. Our recent work shows that this 'animal model' represents a very useful tool for studying how LCC happens in humans, already providing new clues about the function of U8. In this project we want to do more experiments, including using our zebrafish, to try to find out why U8 is so important for keeping the blood vessels in our brain healthy, and how problems with the working of U8 cause the disease LCC. We think that this could be relevant not only for the development of future treatments in LCC, but also for our understanding of more common diseases involving the brain blood vessels, such as stroke.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1101/gr.275900.121
发表时间:
2022-05
期刊:
GENOME RESEARCH
影响因子:
7
作者:
[Gabryelska, Marta M., Badrock, Andrew P., Lau, Jian You, O'Keefe, Raymond T., Crow, Yanick J., Kudla, Grzegorz]
通讯作者:
Kudla, Grzegorz
Genetic disorders of human neurological and immune function
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批准号:MC_UU_00035/11
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项目类别:Intramural
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资助金额:$581.93万
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财政年份:2023
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负责人:Yanick Crow
-
依托单位:
Replication-dependent histone pre-mRNA misprocessing and innate immune sensing
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批准号:MR/V000195/1
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项目类别:Research Grant
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资助金额:$79.91万
-
财政年份:2020
-
负责人:Yanick Crow
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依托单位:
Inhibition of reverse transcription in type I interferon mediated neuropathology
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批准号:MR/S034676/1
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项目类别:Research Grant
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资助金额:$219.09万
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财政年份:2020
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负责人:Yanick Crow
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依托单位:
ERA-NET NEURON: Investigation of the neuroinflammatory basis of the human type I
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批准号:MR/M501803/1
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项目类别:Research Grant
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资助金额:$35.62万
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财政年份:2015
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负责人:Yanick Crow
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依托单位:
国内基金
海外基金
PfAP2-R介导的PfCRT转录调控在恶性疟原虫对喹啉类药物抗性中的作用及机制研究
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批准号:82372275
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项目类别:面上项目
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资助金额:49.00万元
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批准年份:2023
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负责人:刘耀宝
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依托单位:
Sestrin2抑制内质网应激对早产儿视网膜病变的调控作用及其机制研究
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批准号:82371070
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项目类别:面上项目
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资助金额:49.00万元
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批准年份:2023
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负责人:赵培泉
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依托单位: