塔斯马尼亚魔鬼两种传染性癌症的演变
Maximilian R Stammnitz1, Kevin Gori1, Young Mi Kwon1
1Transmissible Cancer Group, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
概括
塔斯马尼亚恶魔有两种传染性癌症, 基因分析揭示了它们独特的进化路径和突变率, 突出了这些独特的癌症系的平行进化.
科学领域:
- 基因组学
- 进化生物学
- 癌症研究
背景情况:
- 塔斯马尼亚魔鬼因两种可传播的癌症而面临灭绝:魔鬼面部瘤1 (DFT1) 和魔鬼面部瘤2 (DFT2).
- 了解这些传染性癌症的遗传多样性和演变对于保护工作至关重要.
研究的目的:
- 研究DFT1和DFT2的遗传多样性和进化轨迹.
- 为了比较突变率并确定对这些传染性癌症的选择压力.
主要方法:
- 使用新的染色体水平基因组分析78个DFT1和41个DFT2.
- 时间解析的基因分析以估计出现日期.
- 亚克隆分析以评估种群异质性和突变率.
主要成果:
- DFT1在1986年 (1982年至1989年) 出现,而DFT2在2011年 (2009年至2012年) 出现.
- 在所有变种类别中,DFT2的突变率高于DFT1.
- 鉴定出一种具有缺陷DNA不匹配修复的多变异DFT1系.
- 在特定位置发现了阳性选择的证据,包括Y染色体损失和MGA无活化,但这两种癌症都不常见.
结论:
- 尽管DFT1和DFT2的起源和遗传特征不同,但它们的长期演变是平行的.
- 这些发现为单个宿主群体内的传染性癌症的进化动态提供了洞察力.
更多相关视频
05:45In Vitro Establishment of a Genetically Engineered Murine Head and Neck Cancer Cell Line using an Adeno-Associated Virus-Cas9 System
Published on: January 9, 2020
8.0K
07:13Initiation of Metastatic Breast Carcinoma by Targeting of the Ductal Epithelium with Adenovirus-Cre: A Novel Transgenic Mouse Model of Breast Cancer
Published on: March 26, 2014
23.4K
相关概念视频
Rous Sarcoma Virus (RSV) and Cancer
5.2K
Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
5.2K
Mechanisms of Retrovirus-induced Cancers
5.2K
Retroviruses are RNA viruses that have been shown to cause cancers in diverse species, including chickens, mice, cats, and monkeys. The RNA genomes of these viruses are first reverse-transcribed into single and then double-stranded DNA (dsDNA) copies. This dsDNA called proviral DNA then integrates into the host genome. Subsequently, the host cell transcribes the proviral DNA in concert with the chromosomal DNA. This leads to the production of viral RNA and proteins that assemble at the host...
5.2K
Retroviruses
12.6K
Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
12.6K
Viral Recombination
23.6K
Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
23.6K
Viral Mutations
32.7K
A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
32.7K
Convergent Evolution
28.1K
Evolution shapes the features of organisms over time, ensuring that they are suited for the environments in which they live. Sometimes, selection pressure leads to the rise of similar but unrelated adaptations in organisms with no recent common ancestors, a process known as convergent evolution.
28.1K
