Genetics Fundamentals and Mendelian Inheritance
Termini in questo insieme (20)
An allele is a variant form of a gene at a specific locus on a chromosome.
A gene is a unit of heredity that carries information for a specific trait and is made up of DNA.
Inheritance pattern involving a single gene with two alleles, demonstrating dominance and segregation of alleles.
Dominance occurs when one allele masks the expression of another allele at the same locus.
Segregation is the separation of alleles during gamete formation so each gamete carries only one allele.
Exceptions include lethal genes, co-dominance, incomplete dominance, and haploinsufficiency.
Co-dominance is when both alleles in a heterozygote are fully expressed, producing a distinct phenotype for each.
Incomplete dominance occurs when the heterozygote shows an intermediate phenotype between the two homozygotes.
Haploinsufficiency is when a single functional copy of a gene is insufficient to produce a normal phenotype.
Inheritance involving two genes with independent assortment of alleles, producing a 9:3:3:1 phenotypic ratio in F2.
Alleles of different genes assort independently during gamete formation, leading to genetic variation.
Recessive epistasis occurs when the recessive allele of one gene masks the expression of alleles of another gene.
Dominant epistasis happens when a dominant allele of one gene masks the expression of alleles of another gene.
An inhibitory gene suppresses the expression of another gene, affecting phenotype.
Multiple alleles refer to more than two alternative forms of a gene that can occupy the same locus.
The human blood group system (ABO) is a classic example involving multiple alleles.
They interact through dominance, co-dominance, and epistatic interactions to determine blood group phenotypes.
Cytoplasmic inheritance is the transmission of genetic material through cytoplasm, often maternally inherited.
Kappa particles in Paramecia are cytoplasmic elements inherited maternally.
Shell coiling in Limnea is an example of maternal inheritance through cytoplasmic factors.