I think it's B: DNA replication
Parietal lobe and frontal lobe
Answer: Small intestines
Explanation: Digestion of carbohydrates begins in the mouth mechanically and through salivary amylase. It passes down to the stomach by parastalsis, digested further and goes to the small intestines where their absorption begins. Carbohydrates are a source of glucose, that most organs use as their primary energy source. Indigestible carbohydrates and fibers travels down to the large intestines where they are digested by bacteria or eliminated as waste through the anus.
The small intestines consist of microvilli that increase surface area for maximum nutrient absorption. Carbohydrates are absorbed by the small intestines via the jejunum, taken to the blood stream then transported to the liver where glycolysis and most metabolic pathways take place, for energy production.
<span>The answer is a lioness teaching her young how to hunt
An action could be considered as a reproductive strategy is it's being done to ensure the continuation of the next generation.
Teaching the young lion to hunt will definitely improve the young lion capability's to survive and help their survivability</span>
In human gene therapy, a genetically modified virus (a.k.a. a viral vector) can alter the genetic variation of a cell, but not all viral vectors do.
The process often begins with the delivery of or creation of a segment of viral double stranded DNA (containing the gene you want to introduce). Then typically an enzyme known as an integrase cuts the ends of the segment of viral DNA and also cuts open the cell's DNA. Then the viral DNA is integrated/ inserted into the cell's DNA. The connecting ends are ligated together and adjusted so that the nucleotide base pairs match up.
This in the future may affect the gene pool for instance if the viral DNA (your gene) was inserted in the middle of another gene or important regulatory sequence of the cell DNA, and this alteration may be passed on into offspring and become present in the gene pool, which could have bad effects.
The effects on the gene pool really depends on what the virus ends up doing. For example, it may fix the function of a damaged gene which is the goal, and allow for a working gene to be in the gene pool, which would be good. The problem with gene therapy is that it's difficult to predict 100% what the virus will do every time it is given to a patient.
But it's very important to consider that it will only affect the gene pool if the virus is able to enter and alter germ cells (reproductive cells). If the virus, enters somatic cells (regular body cells) this will not be passed on to future generations. So viruses can be designed to avoid germ cells and avoid this gene pool issue. Also, some viral vectors use viruses that do not integrate their DNA, the cells just express the viral DNA (create the desired protein from it) and over time the viral DNA is degraded/ lost which wouldn't pose this threat.
This is long, but I hope it helped!
