Answer:
The genotype of the offspring would be heterogeneous.
Explanation:
In four O'clock plants in case of incomplete dominance, no colour is dominant. They are existing in an intermediate character / a new character. This new colour is pink, not white or red.
The white and red colour flowers are wild type and homogenous type. When the cross occurs and incomplete dominance happen, the F1 flower would be pink one but heterogeneous.
Because according to Mendel's deviation, there are such character appears where neither dominant nor the recessive are the only expressive traits. This has seen in incomplete dominance.
In codominance, which is the another Mendelian deviation, where both the characters has expressed. For example the rose flower having both red and white dots in it. The expression two colours / dominant and recessive characters in the flower is called codominance. Because both expresses at the same time. This codominance genotype is also heterogeneous.
Answer:
One of the common genetic disorders is sickle cell anemia, in which 2 recessive alleles must meet to allow for destruction and alteration in the morphology of red blood cells. This usually leads to loss of proper binding of oxygen to hemoglobin and curved, sickle-shaped erythrocytes. The mutation causing this disease occurs in the 6th codon of the HBB gene encoding the hemoglobin subunit β (β-globin), a protein, serving as an integral part of the adult hemoglobin A (HbA), which is a heterotetramer of 2 α chains and 2 β chains that is responsible for binding to the oxygen in the blood. This mutation changes a charged glutamic acid to a hydrophobic valine residue and disrupts the tertiary structure and stability of the hemoglobin molecule. Since in the field of protein intrinsic disorder, charged and polar residues are typically considered as disorder promoting, in opposite to the order-promoting non-polar hydrophobic residues, in this study we attempted to answer a question if intrinsic disorder might have a role in the pathogenesis of sickle cell anemia. To this end, several disorder predictors were utilized to evaluate the presence of intrinsically disordered regions in all subunits of human hemoglobin: α, β, δ, ε, ζ, γ1, and γ2. Then, structural analysis was completed by using the SWISS-MODEL Repository to visualize the outputs of the disorder predictors. Finally, Uniprot STRING and D2P2 were used to determine biochemical interactome and protein partners for each hemoglobin subunit along with analyzing their posttranslational modifications. All these properties were used to determine any differences between the 6 different types of subunits of hemoglobin and to correlate the mutation leading to sickle cell anemia with intrinsic disorder propensity.
Explanation:
Answer:
Spongy bone
Explanation:
The bone density is reduced and allows the end of bones to compress when stress is applied
Answer:
Extra glucose is stored in the liver as the large compound called glycogen.
Explanation:
