When the plant change its direction towards sunlight
The genetic basis for lactose intolerance is a change in the nucleotide sequence outside of the lactase gene.
Lactose is normally hydrolyzed and broken down in the small intestine.
Lactose intolerance is due to mutations in the MCM6 gene, which regulates the expression of the lactase gene associated with the persistence of enzyme activity in adults.
The lactase enzyme is synthesized from the expression of the LCT gene.
The expression of the LCT gene is regulated by a protein complex (MCM), which is partly encoded by a specific sequence of the MCM6 gene located on chromosome 2q21.
A genetic alteration of this gene, specifically in position 13910, is responsible for the persistence or non-persistence of lactase in the adult.
The nucleotide sequence C / C (Cytosine / Cytosine) would be the one present in the non-persistence of lactase.
Therefore, we can conclude that lactose intolerance is due to a decrease or absence of the activity of the lactase enzyme and that it is due to a change in the nucleotide sequence that helps to control the expression of the LCT gene.
Learn more about lactose intolerance here: brainly.com/question/17178339
Answer:
The majority of the cell membrane is composed of PHOSPHOLIPIDS.
Explanation:
Phospholipids are a type of lipid that is found in the cell membrane of cells. This type of lipid are a good fit for cell membrane because they have the capacity to form bi layers. The lipids are divided into tail and head regions; the head is hydrophilic in nature while the tail is hydrophobic in nature. The hyrophilic head is made up of phosphate group while the hydrophobic tail is made up of fatty acid molecules.
Answer:
its si
Explanation:
Silicon is a chemical element with the symbol Si and atomic number 14. It is a hard, brittle crystalline solid with a blue-grey metallic lustre, and is a tetravalent metalloid and semiconductor. It is a member of group 14 in the periodic table: carbon is above it; and germanium, tin, and lead are below it.