This is called a frameshift mutation....
Losing one nucleotide would cause the entire framework of codons (the 3 nucleotide set that codes for the amino acids) to move off by 1 which results in likely completely different amino acids being called for when the protein is built.
In the case of CF, the normal CFTR gene which codes for Cystic Fibrosis Transmembrane Receptor - a membrane protein, with a point mutation would not be made properly and is therefore not placed into the membrane of the cells of the offspring - this protein is very important in moving sodium into the cell - if this is messed up it results in disease.
Note that CF can result in a number of different types of mutations to the CFTR gene...a frameshift mutation is just one way.
Answer:
Option "C" is correct.
Explanation:
The reason is that, form the two experiments it was concluded that both O1 and O2 were recessive, so all these remaining options which says that any or both of them are dominant are incorrect.
There are so many examples for that in different areas, like biology experiment carried out in our lab recently.
Here's one link: https://www.creative-biogene.com/Services/Custom-Viral-Service/Replication-Competent-Virus-Testing.html
Answer:
Cell division is a process that makes our skin, tissues, muscles, sex cells. It is the building block of our body.
Explanation:
When parents cells ahs been divided into two or more than two daughter cells then it is called division of cells. The division of cells occur as a larger cell. When we talk about eukaryotic cells, these cells divided into two distinct types of the cells, the vegetative cells.
The daughter cells are the identical to the parents cells genetically. There are two types of division such as mitosis and meiosis. When parents cells divides in daughter cells and daughter cells divided further, this process called the cells cycle. The mitosis cell division occur interphase. Meiosis cell division occur in two phase meiosis I and meiosis II.
