哺乳动物进化和人类突变负担在Rab GTPases中
Unmani Sidor1,2, Graham M Hughes1, Jeremy C Simpson1,2
1School of Biology and Environmental Science, University College Dublin, Dublin 4, Ireland.
Biochemistry and biophysics reports
|March 9, 2026
概括
拉布GTPases对于细胞功能至关重要. 这项研究表明,子在更多哺乳动物物种中进化,在人类中积累了更多有害的突变,特别是在Switch I领域,影响了疾病的相关性.
科学领域:
- 分子生物学分子生物学
- 进化生物学 进化生物学
- 遗传学 是一个遗传学.
背景情况:
- 拉布GTPases调节膜贩运,并与神经退行和癌症有关.
- 之前的研究主要集中在单独的鼠身上,并没有研究到家族层面的进化和突变模式.
研究的目的:
- 在哺乳动物进化过程中调查Rab GTPases的进化模式.
- 整合进化发现与人类疾病相关突变在Rabs.
- 在人口层面评估Rab蛋白域的变异耐受性.
主要方法:
- 在62种胎盘哺乳动物中分析了54种Rab蛋白,使用分支站点模型进行序列演变.
- 结合了UniProt. 的进化数据与人类Rab突变数据.
- 定义的域级指标:约束得分,损害耐受性和突变负担.
主要成果:
- 子在更多哺乳动物物种中进化,在人类中增加了有害突变的积累.
- 切换I域表现出显著的跨物种变异,并适应了与疾病相关的突变.
- 域级指标显示了Rab蛋白和域间对变异的不同耐受性.
结论:
- 拉布斯的进化分歧与人类的突变负担相关,特别是在功能关键领域,如Switch I.
- 交换机I域是理解Rab功能,进化和疾病关联的关键区域.
- 综合框架可以应用于其他参与人类疾病的蛋白质家族.
相关概念视频
The Ras Gene
7.4K
The Ras-gene-encoded proteins are regulators of signaling pathways controlling cell proliferation, differentiation, or cell survival. The Ras-gene family in humans constitutes three primary members—the HRas, NRas, and KRas. These genes code for four functionally distinct yet closely related proteins—the HRas, NRas, KRas4A, and KRas4B. The involvement of mutant Ras genes in human cancer was first discovered in 1982 and is among the most common causes of human tumorigenesis.
Ras is a...
Ras is a...
7.4K
Small GTPases - Ras and Rho
5.6K
Ras and Rho are small monomeric GTPases that act downstream of receptor tyrosine kinase (RTK) and regulate various cellular processes. These GTPases switch between active and inactive states by binding to guanine nucleotides.
Three regulatory proteins control their activity:
Three regulatory proteins control their activity:
5.6K
Mutations in Microorganisms
929
Mutations are heritable changes in an organism’s genome involving alterations in the base sequence of DNA or RNA. These changes can influence cellular processes and phenotypic traits, potentially transforming the unaltered wild type into a mutant form. Such changes, termed forward mutations, are pivotal in shaping the genetic diversity of organisms.RNA viruses exhibit the highest mutation rates due to the absence of robust proofreading mechanisms during genome replication. In contrast,...
929
Mismatch Repair
6.8K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
6.8K
Mismatch Repair
44.4K
Overview
44.4K
Rab Proteins
5.3K
Rab proteins constitute the largest family of monomeric GTPases, of which 70 members are present in humans. Rab proteins and their effectors regulate consecutive stages of vesicle transport such as vesicle transport, docking, and fusion to the correct recipient membrane.
Rab proteins switch between a cytosolic, GDP-bound inactive state and a membrane-anchored, GTP-bound active state. By themselves, Rabs show slow rates of GDP/GTP exchange and GTP hydrolysis. Thus, Rab proteins are considered...
Rab proteins switch between a cytosolic, GDP-bound inactive state and a membrane-anchored, GTP-bound active state. By themselves, Rabs show slow rates of GDP/GTP exchange and GTP hydrolysis. Thus, Rab proteins are considered...
5.3K


