The new LAW of microRNA-mediated gene silencing
The new LAW of microRNA-mediated gene silencing
批准号:
BB/I007571/2
负责人:
Tyson Sharp
金额:
$60.13万
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
项目状态:
已结题
起止时间:
2012 至 --
中文摘要
MicroRNAs(MiRNAs)是最近被发现抑制基因表达的一类存在于人体所有细胞中的小RNA。它们的作用机制是深远和复杂的;每个miRNA可能控制许多基因,据估计,miRNAs调控多达三分之一的人类基因的表达。人类基因通过一种信使核糖核酸中间体以蛋白质的形式表达,该中间体是DNA编码基因的拷贝。然后,这种信使核糖核酸从细胞核进入细胞质,在那里密码被‘翻译’或被制造成蛋白质,从而被表达。MicroRNAs通过两种假设机制之一来抑制基因的表达:(1)与一条mRNA配对,并在其翻译为蛋白质的早期停止其表达,即起始阻断;(2)与靶mRNA配对--在其翻译为蛋白质的过程中停止表达,从而停止蛋白质的产生,即后起始阻断。在任何一种情况下,信使核糖核酸都不被翻译成蛋白质,而是(被抑制),但信使核糖核酸保持不变。MicroRNAs在不同的生物体、细胞发育阶段和疾病模型中表现出不同的表达模式,在调节基因表达方面发挥着重要作用。尽管近年来我们已经学到了很多关于miRNA生物学的知识,但我们仍然不知道细胞如何执行miRNA介导的基因沉默的确切机制(S),以及它如何在不同类型的miRNA沉默(启动或启动后阻断)之间做出决定。我的研究小组已经确定了两组不同的蛋白质,(1)被称为LIMD1,Ajuba,WTIP(法律)和(2)被称为Zysin,LPP,TRIP6(ZLT)。我们认为,这可能代表了使miRNA指导的基因沉默缺失的组件。此外,这两组蛋白质可以帮助细胞决定执行哪种类型的miRNA沉默。使用法律小组和使用启蒙阻滞剂,或使用ZLT组并诱导启蒙后阻滞剂。我们的研究旨在确定这些可能性,从而确定最终将对改善人类和动物健康产生长期影响的新生物学。
英文摘要
MicroRNAs (miRNAs) are a class of small RNAs within all the cells of our body that have recently been found to inhibit gene expression. Their mechanism of action is far reaching and complex; each miRNA may control many genes and it is estimated that miRNAs regulate expression of up to 1/3 of all human genes. Human genes are expressed as proteins via a mRNA intermediate which is a copy of the DNA encoded gene in question. This mRNA then travels from the nucleus to the cytoplasm where the code is 'translated' or made into protein and thus expressed. MicroRNAs operate to inhibit gene expression by one of two hypothesised mechanisms: (1) by pairing with a mRNA- and stopping the mRNA being expressed very early on in its translation into protein, initiation block and (2) pairing with target mRNA - stopping the mRNA being expressed in the middle of its translation into protein therefore halting protein production, post-initiation block. In either case the mRNA is not translated into protein but (repressed) but the mRNA remains intact. MicroRNAs show distinct expression patterns in different organisms, cell development stages, and disease models and play an important role in regulating gene expression. Even though we have learnt a great deal about miRNA biology in recent years we still do not know the precise mechanism(s) of how the cell performs miRNA-mediated gene silencing and furthermore how it decides between the different types of miRNA silencing (initiation or post-initiation block). My research group has identified two distinct groups of proteins, (1) called LIMD1, Ajuba, WTIP (LAW) and (2) called Zyxin, LPP, TRIP6 (ZLT). Which we believe may represent the missing components to enable miRNA-directed gene silencing. Furthermore, these two groups of protein may then help the cell decide which type of miRNA silencing to perform. Employ the LAW group and use initiation block, or the ZLT group and induce a post-initiation block. Our research is aimed at determining these possibilities and therefore new biology which will ultimately impact on improved human and animal health in the long term.
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DOI:
10.1016/j.celrep.2017.06.027
发表时间:
2017-07-05
期刊:
Cell reports
影响因子:
8.8
作者:
[Bridge KS, Shah KM, Li Y, Foxler DE, Wong SCK, Miller DC, Davidson KM, Foster JG, Rose R, Hodgkinson MR, Ribeiro PS, Aboobaker AA, Yashiro K, Wang X, Graves PR, Plevin MJ, Lagos D, Sharp TV]
通讯作者:
Sharp TV
DOI:
10.1016/j.biocel.2015.10.006
发表时间:
2015-12
期刊:
The international journal of biochemistry & cell biology
影响因子:
--
作者:
[Leonov G, Shah K, Yee D, Timmis J, Sharp TV, Lagos D]
通讯作者:
Lagos D
DOI:
10.18632/oncotarget.23676
发表时间:
2018-01-19
期刊:
Oncotarget
影响因子:
--
作者:
[Wang L, Howell MEA, McPeak B, Riggs K, Kohne C, Yohanon JU, Foxler DE, Sharp TV, Moorman JP, Yao ZQ, Ning S]
通讯作者:
Ning S
DOI:
10.1158/0008-5472.can-15-3134
发表时间:
2016-08-15
期刊:
Cancer research
影响因子:
11.2
作者:
[Feber A, Worth DC, Chakravarthy A, de Winter P, Shah K, Arya M, Saqib M, Nigam R, Malone PR, Tan WS, Rodney S, Freeman A, Jameson C, Wilson GA, Powles T, Beck S, Fenton T, Sharp TV, Muneer A, Kelly JD]
通讯作者:
Kelly JD
DOI:
10.1093/nar/gkw631
发表时间:
2016-11-16
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Warner MJ, Bridge KS, Hewitson JP, Hodgkinson MR, Heyam A, Massa BC, Haslam JC, Chatzifrangkeskou M, Evans GJ, Plevin MJ, Sharp TV, Lagos D]
通讯作者:
Lagos D
The Lexicon of miRISC: Deconstructing the functional complexity of the miRNA induced silencing complex
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批准号:BB/V009567/1
-
项目类别:Research Grant
-
资助金额:$67.22万
-
财政年份:2022
-
负责人:Tyson Sharp
-
依托单位:
Unravelling the Mechanism of the Lung Tumour Suppressor LIMD1 from Cellular Metabolism to Malignant Transformation.
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批准号:MR/N009185/1
-
项目类别:Research Grant
-
资助金额:$48.45万
-
财政年份:2016
-
负责人:Tyson Sharp
-
依托单位:
Characterisation of a new mechanism of regulation for HIF1 and the hypoxic response.
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批准号:BB/L027755/1
-
项目类别:Research Grant
-
资助金额:$42.72万
-
财政年份:2014
-
负责人:Tyson Sharp
-
依托单位:
Taiwan and UK International Partnership towards the advancement and discovery of novel microRNA species and regulatory proteins in stem cell biology.
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批准号:BB/L003945/1
-
项目类别:Research Grant
-
资助金额:$3.17万
-
财政年份:2013
-
负责人:Tyson Sharp
-
依托单位:
Pre-commercialisation validation of Stem Cell Generator as a highly efficient single transfection iPSC reprogramming vector
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批准号:BB/J010901/1
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项目类别:Research Grant
-
资助金额:$14.59万
-
财政年份:2012
-
负责人:Tyson Sharp
-
依托单位:
The new LAW of microRNA-mediated gene silencing
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批准号:BB/I007571/1
-
项目类别:Research Grant
-
资助金额:$74.11万
-
财政年份:2011
-
负责人:Tyson Sharp
-
依托单位:
Spatio-temporal structural and functional studies into the novel interaction between LIMD1 and clathrin heavy chain proteins
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批准号:BB/F006470/1
-
项目类别:Research Grant
-
资助金额:$41.79万
-
财政年份:2008
-
负责人:Tyson Sharp
-
依托单位:
国内基金
海外基金
低表面亮度星系的恒星形成指标之间的相关性以及Kennicutt-Schmidt Law的研究
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批准号:12003043
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项目类别:青年科学基金项目
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资助金额:24.0万元
-
批准年份:2020
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负责人:雷凤杰
-
依托单位:
约化群酉表示的branching law及其应用
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批准号:10971103
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项目类别:面上项目
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资助金额:24.0万元
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批准年份:2009
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负责人:朱富海
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依托单位: