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Investigating the role of the U2 and U6 snRNAs in exon ligation during pre-mRNA splicing

Investigating the role of the U2 and U6 snRNAs in exon ligation during pre-mRNA splicing
研究 U2 和 U6 snRNA 在前 mRNA 剪接过程中外显子连接中的作用
批准号:
BB/E000436/1
负责人:
Raymond O'Keefe
金额:
$35.07万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2006
资助国家:
英国
项目状态:
已结题
起止时间:
2006 至 --

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中文摘要
翻译
细胞的DNA被复制到前信使RNA(前信使RNA)中,细胞将其用作蛋白质生产的模板。DNA中包含的所有信息并不是制造蛋白质所必需的,因此,在制造蛋白质之前必须去除不需要的信息。不想要的信息通过类似于剪辑电影中不想要的帧的过程从前信使核糖核酸中移除或‘拼接’。这种前信使核糖核酸的‘剪接’是非常重要的,因为它必须准确地发生,才能产生功能蛋白。即使是一个核苷酸的错误也可能对最终产生的蛋白质产生灾难性的影响。“剪接”的过程是由一个叫做剪接体的大型RNA/蛋白质复合体完成的。剪接体与前信使核糖核酸相互作用,识别并“拼接”出不想要的区域。越来越多的证据表明,剪接体的RNA成分对剪接的实际切割过程至关重要。在这项研究拨款的期限内将开展的工作将解决剪接体的RNA组件如何相互作用以及如何与前-mRNA相互作用,以识别并‘拼接’出不需要的区域。这是一项基础研究,将有助于我们了解一个关键的细胞过程。
英文摘要
The DNA of a cell is copied into a pre-messenger RNA (pre-mRNA) that the cell uses as a template for protein production. All the information contained in DNA is not required for making proteins, therefore, unwanted information must be removed before a protein is made. The unwanted information is removed, or 'spliced', from pre-mRNA by a process similar to the editing of unwanted frames from a film. This 'splicing' of the pre-mRNA is very important because it must occur accurately in order for functional proteins to be produced. A mistake by even one nucleotide could have disastrous effects on the final protein produced. The process of 'splicing' is carried out by a large RNA/protein complex called the spliceosome. The spliceosome interacts with the pre-mRNA to identify and 'splice' out the unwanted regions. An increasing amount of evidence points to the RNA components of the spliceosome as being critical for the actual cutting process of splicing. The work that will be undertaken during the tenure of this research grant will address how the RNA components of the spliceosome interact with each other and the pre-mRNA to identify then 'splice' out the unwanted regions. This is basic research that will contribute to our knowledge of a critical cellular process.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1007/978-1-62703-113-4_19
发表时间: 2012
期刊: Methods in molecular biology (Clifton, N.J.)
影响因子: --
作者: [Kershaw, Christopher J, O'Keefe, Raymond T]
通讯作者: O'Keefe, Raymond T
DOI: 10.1093/nar/gkm1098
发表时间: 2008-02
期刊: Nucleic acids research
影响因子: 14.9
作者: [McGrail JC, O'Keefe RT]
通讯作者: O'Keefe RT
DOI: 10.1042/bst0381110
发表时间: 2010-08
期刊: Biochemical Society transactions
影响因子: 3.9
作者: [Hogg R, McGrail JC, O'Keefe RT]
通讯作者: O'Keefe RT
Understanding pre-mRNA splicing regulation with novel inhibitors
  • 批准号:
    BB/S00047X/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $77.07万
  • 财政年份:
    2019
  • 负责人:
    Raymond O'Keefe
  • 依托单位:
Understanding the role of U5 snRNP gene mutation in pre-messenger RNA splicing and craniofacial development
  • 批准号:
    BB/N000358/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $57.44万
  • 财政年份:
    2016
  • 负责人:
    Raymond O'Keefe
  • 依托单位:
Regulation of pre-mRNA splicing fidelity by the Nineteen Complex (NTC)
  • 批准号:
    BB/I019510/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $40.04万
  • 财政年份:
    2012
  • 负责人:
    Raymond O'Keefe
  • 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
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
  • 批准号:
    82371070
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    赵培泉
  • 依托单位: