Connecting the worlds of engineering and regenerative medicine is no small feat and I hope that our last blog, which connected the human brain and the controller of an automation system, opened your eyes and allowed you to make some realistic associations between two distinct processes. With these blogs, we are propelling the industry forward by familiarizing both engineers and scientists with the worlds of a “different” industry.
Answer:Human height
Explanation:
Inheritance patterns are often more complex than predicted by simple mendalian genetics. When Mendel studied some phenotypic characters, like the human skin color and height, they were found to be an addictive effect of two or more genes on a single phenotypic character. These are called quantitative characters, which usually indicates polygenic inheritance.
The human height is an example of quantitative character, it is controlled by at least 3 genes having 6 alleles. 3 genes with 6 alleles from both parent can give rise to wide range of phenotypic character (heights).
The mutation in the somatic cells is known as somatic mutations. As they do not take place in the cells, which give rise to gametes, thus, the mutation is not inherited to the next generation by the sexual means.
On the other hand, the genetic mutations take place in the germline cells, that is, egg and sperm, because of this the mutations possesses the tendency to get passed on from one generation to another.
Thus, mutations are only passed on to offspring when they take place in germ cell DNA. The other kind of cells, the somatic cells refers to the rest of the cells in the body and mutations, which takes place in these cells do not get inherited further to the offspring.
Hence, the correct statements are mutations to gametes can be passed on to an organism's offspring and mutations to somatic cells are only present in the type of cell in which the mutation occurred.