Avoiding replication trainwrecks - are accessory replicative helicases needed to underpin replication of protein-bound DNA?
Avoiding replication trainwrecks - are accessory replicative helicases needed to underpin replication of protein-bound DNA?
批准号:
BB/G005915/1
负责人:
Peter McGlynn
金额:
$38.52万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2009
资助国家:
英国
项目状态:
已结题
起止时间:
2009 至 --
中文摘要
一个有机体要生长,它的细胞必须分裂和繁殖。但是,一个细胞要分裂成两个细胞,需要复制该细胞内的遗传物质。这使得两个子细胞都能继承遗传蓝图的完整副本。没有这个蓝图,细胞就不能正常工作,最终会死亡。不幸的是,复制细胞的遗传物质是一个非常复杂的过程,部分原因是即使是细菌这样的简单生物体也需要大量的DNA来携带遗传密码。这一过程的复杂性及其至关重要性导致了非常复杂的细胞机器的进化,这些机器可以复制细胞中发现的大量DNA。这些细胞机器可以非常快速和准确地复制DNA。然而,我们现在知道,这些机器并不完美,在试图复制遗传密码时经常发生故障。它们为什么会坏掉?一个主要的问题是环境中的某些化学物质以及太阳紫外线等辐射对DNA的损害。但另一个问题可能是由细胞本身引起的。携带遗传密码的DNA实际上并不孤立地存在于细胞内,而是完全被称为蛋白质的分子所包裹。这些蛋白质几乎对细胞内的每一个过程都是必不可少的,因此在这些蛋白质的必要性和复制DNA的必要性之间存在冲突。我们自己和其他人的工作已经证明,这些蛋白质可以阻止DNA被复制。我们最近发现,细胞内的某些酶(称为DNA解旋酶)可能有助于DNA的复制,通过促进DNA复制机通过蛋白质-DNA复合物的运动。这项研究的目的是确定这些酶是否确实促进DNA的复制,以及这些酶的哪些功能是实现这种功能所必需的。这将通过研究这些酶的分离和细胞内的情况下实现。这些研究可能有助于我们了解细胞如何在面对许多潜在的障碍时复制其遗传物质。DNA复制的阻断对细胞来说可能是灾难性的。DNA复制失败会阻止细胞分裂产生两个可行的子细胞。但堵塞也会导致DNA复制过程中的错误。这些错误会导致子细胞发生突变和随之而来的功能障碍。在包括人类在内的复杂生物体中,这些功能障碍可能以遗传疾病和癌症的形式出现。我们的工作将有助于了解如何将这些风险降至最低。
英文摘要
For an organism to grow it is necessary that the cells of that organism divide and multiply. But for a cell to divide into two requires that the genetic material within that cell is copied. This allows both daughter cells to inherit a complete copy of the genetic blueprint. Without this blueprint a cell cannot function correctly and will die ultimately. Unfortunately, copying the genetic material of a cell is a very complex process, in part because there is a huge amount of DNA needed to carry the genetic code of even a simple organism such as a bacterium. The complexity of this process, and its critical importance, has led to the evolution of very complex cellular machines that can duplicate the large amounts of DNA found in cells. These cellular machines can copy the DNA very rapidly and very accurately. However, we now know that these machines are not perfect and often break down whilst trying to copy the genetic code. Why do they break down? One major problem is damage to the DNA caused by certain chemicals in the environment and also by radiation such as ultraviolet light from the sun. But another problem might be caused by the cell itself. The DNA carrying the genetic code does not actually exist in isolation within the cell but is completely coated in molecules called proteins. These proteins are essential for nearly every process within the cell and so a conflict exists between the necessity for these proteins and the need to copy the DNA. Our own, and others', work has demonstrated that these proteins can stop the DNA from being copied. We have recently discovered that certain enzymes within a cell (called DNA helicases) might help during duplication of DNA by facilitating the movement of DNA copying machines through protein-DNA complexes. This study aims to establish whether these enzymes do promote copying of DNA and what features of these enzymes are needed for such a function. This will be achieved by studying these enzymes in isolation and also within the context of the cell. These studies may help us to understand how cells duplicate their genetic material in the face of many potential blocks. Blockage of DNA copying is potentially catastrophic for a cell. Failure to copy the DNA prevents a cell from dividing to give two viable daughter cells. But blockage can also lead to errors during this DNA copying process. These errors can cause mutations and consequent malfunctions in daughter cells. In complex organisms, including humans, these malfunctions can take the form of genetic diseases and the onset of cancer. Our work will help understand how these risks might be minimised.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1093/nar/gkq889
发表时间:
2011-02
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Atkinson J, Gupta MK, Rudolph CJ, Bell H, Lloyd RG, McGlynn P]
通讯作者:
McGlynn P
DOI:
10.1093/nar/gkq975
发表时间:
2011-03
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Atkinson J, Gupta MK, McGlynn P]
通讯作者:
McGlynn P
Helicases that underpin replication of protein-bound DNA in Escherichia coli.
支持大肠杆菌中蛋白质结合 DNA 复制的解旋酶。
DOI:
10.1042/bst0390606
发表时间:
2011
期刊:
Biochemical Society transactions
影响因子:
3.9
作者:
[McGlynn P]
通讯作者:
McGlynn P
Speeding and stuttering: analysing the dynamics of DNA replication at the single molecule level
-
批准号:BB/K00168X/1
-
项目类别:Research Grant
-
资助金额:$38.38万
-
财政年份:2013
-
负责人:Peter McGlynn
-
依托单位:
Recombination and the clearance of replicative blocks - to bypass or not to bypass?
-
批准号:BB/J014826/1
-
项目类别:Research Grant
-
资助金额:$40.73万
-
财政年份:2013
-
负责人:Peter McGlynn
-
依托单位:
Why does transcription present a major barrier to genome duplication?
-
批准号:BB/I001859/2
-
项目类别:Research Grant
-
资助金额:$19.32万
-
财政年份:2012
-
负责人:Peter McGlynn
-
依托单位:
Why does transcription present a major barrier to genome duplication?
-
批准号:BB/I001859/1
-
项目类别:Research Grant
-
资助金额:$36.88万
-
财政年份:2011
-
负责人:Peter McGlynn
-
依托单位:
Conflicts between DNA replication fork progression and transcriptional regulation
-
批准号:BB/C008316/1
-
项目类别:Research Grant
-
资助金额:$30.49万
-
财政年份:2006
-
负责人:Peter McGlynn
-
依托单位:
High performance motoring - replication fork movement in a complex environment
-
批准号:G0501626/1
-
项目类别:Research Grant
-
资助金额:$40.47万
-
财政年份:2006
-
负责人:Peter McGlynn
-
依托单位:
国内基金
海外基金
登录
查看更多内容
SETD3甲基化修饰MCM复合体调控DNA复制的分子机制
-
批准号:32200584
-
项目类别:青年科学基金项目(C类)
-
资助金额:20.0万元
-
批准年份:2022
-
负责人:赵梦洁
-
依托单位:
新的FANCM关联蛋白复合物FMAP150-FMAP160调控FANCM修复停滞复制叉的作用及机制
-
批准号:32070716
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2020
-
负责人:ZHIJIANG YAN
-
依托单位:
小鼠Pold4介导的基因组稳定性在肺癌发生发展中的功能和机制研究
-
批准号:31900512
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2019
-
负责人:周忠诚
-
依托单位:
植物基因重组频率的遗传调控
-
批准号:31930018
-
项目类别:重点项目
-
资助金额:300.0万元
-
批准年份:2019
-
负责人:程祝宽
-
依托单位:
基于DNA纤维荧光原位杂交技术的DNA交联损伤修复研究
-
批准号:31871365
-
项目类别:面上项目
-
资助金额:59.0万元
-
批准年份:2018
-
负责人:黄静
-
依托单位:
对Rad18和Rad5的结构和功能研究
-
批准号:31070653
-
项目类别:面上项目
-
资助金额:8.0万元
-
批准年份:2010
-
负责人:向嵩
-
依托单位:
miRNA-501和let-7a促进HBV复制的机制研究
-
批准号:30970149
-
项目类别:面上项目
-
资助金额:30.0万元
-
批准年份:2009
-
负责人:时永全
-
依托单位: