普莱奥特罗皮和完美的保存
1D. Waxman, Centre for the Study of Evolution and Centre for Theoretical Physics, University of Sussex, Brighton, BN1 UK. J. R. Peck, Centre for the Study of Evolution and School of Biological Sciences, University of Sussex, Brighton, BN1.
概括
一个数学模型表明,一个突变可以影响选择下的多个特征. 当三个或更多的特征受到影响时,单一的遗传序列可以成为主导,解释低遗传变异.
科学领域:
- 进化生物学是进化的生物学.
- 人口遗传学 人口遗传学
- 数学建模的数学建模
背景情况:
- 表型变异受遗传突变的影响.
- 稳定选择对多种表型特征起作用.
- 了解特征变异的遗传基础至关重要.
研究的目的:
- 开发一种数学模型,解释单个突变如何影响多个特征.
- 在稳定选择下,研究影响多个特征的突变的进化后果.
- 为观察到的低遗传变异和替代率提出假设解释.
主要方法:
- 开发了一种数学模型,其中包含了影响多个表型特征的单个突变.
- 在每个字符的选择稳定条件下分析模型.
- 允许广泛的突变,包括具有轻微表型影响的突变.
主要成果:
- 证明影响三种或更多特征的突变可以导致单个最佳遗传序列变得普遍.
- 表明受影响的字符的数量是决定进化结果的关键因素.
- 鉴定了减少遗传变异的条件.
结论:
- 一个影响多个特征的单一突变可以推动进化趋同到一个最佳的遗传序列.
- 该模型为在某些遗传位置观察到的低遗传变异和替代率提供了潜在的解释.
- 这些发现凸显了类在塑造进化轨迹中的重要性.
相关概念视频
Epistasis
In addition to multiple alleles at the same locus influencing traits, numerous genes or alleles at different locations may interact and influence phenotypes in a phenomenon called epistasis. For example, rabbit fur can be black or brown depending on whether the animal is homozygous dominant or heterozygous at a TYRP1 locus. However, if the rabbit is also homozygous recessive at a locus on the tyrosinase gene (TYR), it will have an unshaded coat that appears white, regardless of its TYRP1...
Pleiotropy
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
Hardy-Weinberg Principle
Diploid organisms have two alleles of each gene, one from each parent, in their somatic cells. Therefore, each individual contributes two alleles to the gene pool of the population. The gene pool of a population is the sum of every allele of all genes within that population and has some degree of variation. Genetic variation is typically expressed as a relative frequency, which is the percentage of the total population that has a given allele, genotype or phenotype.In the early 20th century,...
Law of Segregation
When crossing pea plants, Mendel noticed that one of the parental traits would sometimes disappear in the first generation of offspring, called the F1 generation, and could reappear in the next generation (F2). He concluded that one of the traits must be dominant over the other, thereby causing masking of one trait in the F1 generation. When he crossed the F1 plants, he found that 75% of the offspring in the F2 generation had the dominant phenotype, while 25% had the recessive phenotype.
Law of Independent Assortment
While Mendel’s Law of Segregation states that the two alleles for one gene are separated into different gametes, a different question of how different genes are inherited remains. For example, is the gene for tall plants inherited with the gene for green peas? Mendel asked this question by experimenting with a dihybrid cross; a cross in which both parents are homozygous for two distinct traits resulting in an F1 generation that are heterozygous for both traits.
Genome Copying Errors
DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their survival. Therefore, the copying errors are checked and repaired at three levels.


