RNA processing mechanisms control lymphocyte development and activation
RNA加工机制控制淋巴细胞的发育和激活
基本信息
- 批准号:BB/J00152X/1
- 负责人:
- 金额:$ 367.89万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2012
- 资助国家:英国
- 起止时间:2012 至 无数据
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
One of the well recognised features of ageing is an increased susceptibility to infection that is caused by a decline in the function of the immune system. Our immune system forms during foetal development and the early neonatal period and is made up of many types of cells including the white blood cells. These are continuously replenished throughout the life-course from specialised stem cells called haematopoietic stem cells that are found in the bone marrow. The white blood cells can be further divided into lymphocytes and non lymphocytes. Amongst the lymphocytes are B cells which produce antibodies and specialised cells that kill virally infected cells. A class of lymphocyte that develops in an organ called the thymus is called the T cell and this cell co-ordinates the function of antibody producing and killer lymphocytes. One important feature of lymphocytes is that they hold a memory of previous encounters with infections. This has been used to create vaccines which make us immune to diseases without having to suffer the disease. While vaccines work well in young individuals they work poorly, or not at all, in the elderly. Because of the importance of lymphocytes they have been much studied and we have plenty of information on the different stages of development the cells go through as they mature and become stimulated by encounter with antigen (the technical term immunologists use for anything that stimulates the immune system). We know much about the signalling processes that take place inside the cell when receptors on the surface of lymphocytes are triggered. We also know much about a class of genes that encode proteins, called transcription factors, which act as on/off switches for genes in the DNA. Transcription factors convert the information encoded in the DNA sequence of genes into a message, called mRNA, which specifies the order in which amino acids are incorporated into proteins. Our project is aimed at understanding how the mRNA is regulated subsequent to its production. We suspect special proteins, called mRNA binding proteins, physically interact with the mRNA and control how long it remains in the cell and the rate at which it can give rise to new proteins. This type of regulation is called post-transcriptional control and is far less well understood. Our study will ask what the function of these mRNA binding proteins is in lymphocytes and will reveal how they work. Our gaol is to understand how mRNA binding proteins interact with signalling pathways and ultimately with transcription factors to control lymphocytes and the immune response.
衰老的一个众所周知的特征是免疫系统功能下降导致对感染的易感性增加。我们的免疫系统在胎儿发育和新生儿早期形成,由包括白细胞在内的多种细胞组成。这些细胞在整个生命过程中不断地从骨髓中发现的称为造血干细胞的专门干细胞中补充。白细胞又可分为淋巴细胞和非淋巴细胞。淋巴细胞中有产生抗体的B细胞和杀死病毒感染细胞的特化细胞。在胸腺器官中发育的一类淋巴细胞被称为T细胞,这种细胞协调产生抗体和杀伤淋巴细胞的功能。淋巴细胞的一个重要特征是它们对以前的感染有记忆。这已经被用来制造疫苗,使我们对疾病免疫,而不必遭受疾病。虽然疫苗对年轻人很有效,但对老年人却效果很差,或者根本不起作用。由于淋巴细胞的重要性,人们对它们进行了大量的研究,我们对细胞发育的不同阶段有了大量的了解,这些细胞在成熟过程中经历了不同的阶段,并受到抗原的刺激(抗原是免疫学家用来形容任何刺激免疫系统的东西的技术术语)。当淋巴细胞表面的受体被触发时,我们对细胞内发生的信号传导过程了解很多。我们也很了解一类编码蛋白质的基因,称为转录因子,它在DNA中充当基因的开关。转录因子将基因DNA序列中编码的信息转化为信使rna,信使rna指定了氨基酸与蛋白质结合的顺序。我们的项目旨在了解mRNA在其产生后是如何被调节的。我们怀疑一种叫做mRNA结合蛋白的特殊蛋白质与mRNA发生物理相互作用,并控制mRNA在细胞中停留的时间和产生新蛋白质的速度。这种类型的调节被称为转录后控制,人们对其知之甚少。我们的研究将探讨这些mRNA结合蛋白在淋巴细胞中的功能,并揭示它们是如何工作的。我们的目标是了解mRNA结合蛋白如何与信号通路相互作用,最终与转录因子相互作用,以控制淋巴细胞和免疫反应。
项目成果
期刊论文数量(10)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Uncovering the Role of RNA-Binding Proteins in Gene Expression in the Immune System.
- DOI:10.3389/fimmu.2018.01094
- 发表时间:2018
- 期刊:
- 影响因子:7.3
- 作者:Díaz-Muñoz MD;Turner M
- 通讯作者:Turner M
Deletion of AU-rich elements within the Bcl2 3'UTR reduces protein expression and B cell survival in vivo.
- DOI:10.1371/journal.pone.0116899
- 发表时间:2015
- 期刊:
- 影响因子:3.7
- 作者:Díaz-Muñoz MD;Bell SE;Turner M
- 通讯作者:Turner M
The RNA-binding protein HuR is essential for the B cell antibody response.
- DOI:10.1038/ni.3115
- 发表时间:2015-04
- 期刊:
- 影响因子:30.5
- 作者:
- 通讯作者:
Cell cycle RNA regulons coordinating early lymphocyte development.
细胞周期RNA调节,协调早期淋巴细胞发育。
- DOI:10.1002/wrna.1419
- 发表时间:2017-09
- 期刊:
- 影响因子:0
- 作者:Galloway A;Turner M
- 通讯作者:Turner M
Tia1 dependent regulation of mRNA subcellular location and translation controls p53 expression in B cells.
- DOI:10.1038/s41467-017-00454-2
- 发表时间:2017-09-13
- 期刊:
- 影响因子:16.6
- 作者:Díaz-Muñoz MD;Kiselev VY;Le Novère N;Curk T;Ule J;Turner M
- 通讯作者:Turner M
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Martin Turner其他文献
Managing the aftermath of mania - Newcastle, 2 September 2005: Consensus Meeting Statement
管理狂热的后果 - 纽卡斯尔,2005 年 9 月 2 日:共识会议声明
- DOI:
- 发表时间:
2006 - 期刊:
- 影响因子:4.1
- 作者:
A. Young;J. Cookson;Brent Elliott;J. Hellewell;R. H. McAllister;James Newham;Alan Ogilvie;Jan Scott;S. Tyrer;Martin Turner - 通讯作者:
Martin Turner
Psychological predictors of adolescent depression and anxiety symptoms across one season in grassroots netball
草根篮球一赛季中青少年抑郁和焦虑症状的心理预测因素
- DOI:
- 发表时间:
2023 - 期刊:
- 影响因子:0
- 作者:
Lucy E Davies;Martin Turner;Rachel Hopley;Matthew Slater;Elizabeth C. Braithwaite - 通讯作者:
Elizabeth C. Braithwaite
Synergistic activation of PKD by the B cell antigen receptor and CD19 requires PI3K, Vav1 and PLCγ
- DOI:
10.1016/j.cellsig.2005.11.008 - 发表时间:
2006-09-01 - 期刊:
- 影响因子:
- 作者:
Elena Vigorito;Dorottya Kovesdi;Martin Turner - 通讯作者:
Martin Turner
RNA-binding proteins control gene expression and cell fate in the immune system
RNA 结合蛋白控制免疫系统中的基因表达和细胞命运
- DOI:
10.1038/s41590-017-0028-4 - 发表时间:
2018-01-18 - 期刊:
- 影响因子:27.600
- 作者:
Martin Turner;Manuel D. Díaz-Muñoz - 通讯作者:
Manuel D. Díaz-Muñoz
VAV proteins as signal integrators for multi-subunit immune-recognition receptors
变风量(VAV)蛋白作为多亚基免疫识别受体的信号整合体
- DOI:
10.1038/nri840 - 发表时间:
2002-07-01 - 期刊:
- 影响因子:60.900
- 作者:
Martin Turner;Daniel D. Billadeau - 通讯作者:
Daniel D. Billadeau
Martin Turner的其他文献
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{{ truncateString('Martin Turner', 18)}}的其他基金
Mechanisms restraining the accumulation of antibody secreting cells
抑制抗体分泌细胞积累的机制
- 批准号:
BB/W015242/1 - 财政年份:2023
- 资助金额:
$ 367.89万 - 项目类别:
Research Grant
PTBP proteins in T cell activation: Cellular and molecular mechanisms of action
T 细胞激活中的 PTBP 蛋白:细胞和分子作用机制
- 批准号:
BB/P01898X/1 - 财政年份:2017
- 资助金额:
$ 367.89万 - 项目类别:
Research Grant
Testing the Mechanism of T lymphocyte selection in the thymus mediated by the zfp36 family of RNA binding proteins
测试 RNA 结合蛋白 zfp36 家族介导的胸腺中 T 淋巴细胞选择机制
- 批准号:
MR/N010434/1 - 财政年份:2016
- 资助金额:
$ 367.89万 - 项目类别:
Research Grant
Dissecting the molecular mechanisms of PI3K in Extra-Follicular Helper and Regulatory T cell differentiation
剖析 PI3K 在卵泡外辅助细胞和调节性 T 细胞分化中的分子机制
- 批准号:
BB/M021343/1 - 财政年份:2015
- 资助金额:
$ 367.89万 - 项目类别:
Research Grant
Developing The Oxford Study for Biomarkers in Motor Neuron Disease (BioMOx): Capturing pre-symptomatic events and advancing clinical translation
开展运动神经元疾病生物标志物牛津研究 (BioMOx):捕获症状前事件并推进临床转化
- 批准号:
MR/K01014X/1 - 财政年份:2013
- 资助金额:
$ 367.89万 - 项目类别:
Fellowship
transgenic expression of UPRT as a novel tool for tagging RNA in specific tissues of the mouse
UPRT 的转基因表达作为在小鼠特定组织中标记 RNA 的新工具
- 批准号:
BB/K013424/1 - 财政年份:2013
- 资助金额:
$ 367.89万 - 项目类别:
Research Grant
Sampling, biomarker OPtimization and Harmonization In ALS (SOPHIA)
ALS 中的采样、生物标志物优化和协调 (SOPHIA)
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MR/K000780/1 - 财政年份:2012
- 资助金额:
$ 367.89万 - 项目类别:
Research Grant
Cell-intrinsic roles of P110delta in primary and memory antibody responses
P110delta 在初级和记忆抗体反应中的细胞内在作用
- 批准号:
BB/I01246X/1 - 财政年份:2012
- 资助金额:
$ 367.89万 - 项目类别:
Research Grant
PI3Kdelta regulation of influenza virus morbidity
PI3Kdelta 对流感病毒发病率的调节
- 批准号:
G1001068/1 - 财政年份:2011
- 资助金额:
$ 367.89万 - 项目类别:
Research Grant
Methods for Producing T lymphocytes in vitro from Stem Cells
从干细胞体外产生 T 淋巴细胞的方法
- 批准号:
BB/H023690/1 - 财政年份:2010
- 资助金额:
$ 367.89万 - 项目类别:
Research Grant
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