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:
Using some dilutions of the mother solution
Explanation:
If there is a valid process by which the mother solution can be diluted with precision, the results must be in the range that are "normal".
If there are different dilutions that shows different results, but by graphing and extrapolating they show the same results as the mother solution, then the first measurement is correct.
This is also a method used to calibrate an instrument or to confirm the concentration of the mother solution.
check the graph.
Hope this info is useful.
Answer:
Protein synthesis, RNA sequestration, RNA transport and to control transcriptional gene.
Explanation:
The role of non-coding RNAs in transcriptional regulation as well as proteins synthesis etc. Non-coding RNAs is responsible for controlling different processes like protein synthesis, RNA sequestration, RNA transport and to control transcriptional gene through epigenetic regulation and chromatin remodeling. By interacting with DNA, RNA and proteins, non-coding RNAs can regulate chromatin structure and function and the transcription of neighboring.
Due to their structure and function they are differ from each other