It's not sickle-cell itself, but rather being a heterozygous carrier of the disease. People with one dominant and one recessive allele for the disease are immune to malaria without the crippling effects of having sickle-cell anemia. I don't think that it can even represent codominance, though.
The sickle cell allele is caused by a mutation in the HBB gene, which encodes a protein called hemoglobin. This mutation causes an abnormal form of hemoglobin (HbS) to be produced, leading to the characteristic sickle shape of red blood cells in individuals with sickle cell disease.
SS,Ss
V
Yes, the genotype SC refers to individuals who have inherited one sickle cell allele (S) and one C allele, resulting in a sickle cell trait that is different from having sickle cell disease. This genotype can lead to some symptoms similar to sickle cell disease under certain conditions.
Sickle-cell anemia can only be transmitted if both partners have the disease.
Sickle cell disease is an example of codominance, not heterozygous dominance. In individuals who are heterozygous for the sickle cell allele, they exhibit a milder form of the disease called sickle cell trait, which demonstrates codominance of the normal and mutant hemoglobin alleles.
False, Sickle Cell Disease :))
Overdominance is when the heterozygote has an advantage over both the recessive and dominant homozygotes. Sickle cell disease is an example of this. When the individual is homozygous for the sickle cell allele, sickle cell disease is shown. When the the individual is homozygous for the wildtype allele, they appear normal. However, when the individual is heterozygous, he or she appears normal and will also be resistent to malaria.
The absence of the selection pressure malaria. Without selection, in the form of the malarial environment, the sickle cell allele will be lost in the overall US population. Even the heterozygous condition is somewhat deleterious and, statistically without malarial selection pressure the allele will be selected out.
Because individuals who inherit the gene from only one parent produce red blood cells which are distorted. This distortion makes the cells unpalatable to malaria parasites, without seriously harming the individual. This tends to protect against malaria and that protection causes selection for this allele. Individuals who get the sickle cell gene from both parents suffer serious distortion of the red blood cells. This protects against malaria, but also reduces the oxygen-carrying capacity of the red cells to a dangerous degree. This causes a disease called sickle-cell anaemia, which causes selection against the gene. In malarial regions a balance is established. When a population with sickle cell alleles moves to an area with effectively no malaria present, the sickle cell alleles are steadily selected against. This shifts the balance steadily towards low levels.
Normally, the 6th position of the beta chain of hemoglobin is a Glutamic acid, encoded on the DNA as GAG. The sickle cell mutation has the sequence GTG, resulting in a Valine in the 6th position instead.