全基因组再测序揭示了在化过程中选择的位置
Carl-Johan Rubin1, Michael C Zody, Jonas Eriksson
1Department of Medical Biochemistry and Microbiology, Uppsala University, Box 582, SE-75123 Uppsala, Sweden.
Nature
|March 12, 2010
概括
家显示出人类选择的遗传适应,通过基因组测序揭示出来. 关键的遗传变化,如甲状腺刺激激素受体 (TSHR) 位点,影响了肉类和蛋生产的特征.
科学领域:
- 进化遗传学的进化遗传学
- 动物基因组学 动物基因组学
- 化研究 化研究
背景情况:
- 家庭动物是理解表型演变的有价值的模型.
- 人类驱动的选择导致动物形态,生理和行为发生了重大变化.
- 识别这些变化的遗传支提供了对遗传变异在表型多样性中的作用的见解.
研究的目的:
- 为了确定在的化和专业化中涉及的遗传变异,包括选择性扫描和突变.
- 为了研究肉和层之间的差异化遗传基础.
- 增强家禽作为生物医学研究模型的实用性.
主要方法:
- 大规模并行测序基因组.
- 来自8个家禽种群和红色林鸟的基因组DNA分析.
- 单核酸多态 (SNP),删除和选择性扫描的识别.
主要成果:
- 发现了超过7,000,000个SNP和近1,300个删除.
- 在基因组中识别了众多可谓的选择性扫描.
- 在所有家中发现了对甲状腺刺激激素受体 (TSHR) 位点的显著选择性扫除,该位点对新陈代谢和繁殖至关重要.
- 肉的选择性扫除与与生长,食欲和新陈代谢相关的基因有关.
结论:
- 的化和专业化涉及显著的遗传选择,特别是在TSHR位点.
- 对于生长和代谢特征的选择在肉中是显而易见的.
- 功能丧失突变起到了很小的作用,但发现了两个功能性重要的编码删除.
相关概念视频
Genetics of Speciation
19.0K
Speciation is the evolutionary process resulting in the formation of new, distinct species—groups of reproductively isolated populations.
19.0K
Cis-regulatory Sequences
9.5K
Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
9.5K
Incomplete Dominance
19.1K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
19.1K
Multi-species Conserved Sequences
3.3K
Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scale studies have provided new insights into the evolutionary relationship between organisms.
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved...
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved...
3.3K
Genetic Screens
4.6K
Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
4.6K
Complementation Tests
4.9K
A complementation test is a simple cross to identify whether the two mutations are located on the same gene or different genes. It was first performed by Edward Lewis in the 1940s while working on fruit flies. He developed the test to identify the location and arrangement of different mutations on chromosomes.
Organisms heterozygous for different mutations are crossed pairwise in all combinations. If present on different genes, the mutations can complement each other by providing the missing...
Organisms heterozygous for different mutations are crossed pairwise in all combinations. If present on different genes, the mutations can complement each other by providing the missing...
4.9K


