There is no variety in asexual reproduction
Through electrochemical processes
Answer: DF508 mutation. A Genetic, Hereditary, Autosomal and Recessive Mutation.
Explanation:
Cystic fibrosis (CF) is a recessive autosomal lethal disease, it is most common on Caucasoid populations. Its diagnosis is suggested by the clinical features of chronic obstructive pulmonary disease, persistent pulmonary colonization (particularly with mucoid Pseudomonas strains), meconium ileus, pancreatic insufficiency with or familiarity history of the disease. The FC gene is large, with about 250 Kb of genomic DNA, 27 exons representing about 5% of genomic DNA; encodes a 6.5 kb transcribed mRNA. This mRNA is transcribed into a protein of 1480 amino acid called CFTR (Regulator Transmembrane Conductance Cystic Fibrosis). When a three-base pair deletion, adenosine-thymine-thymine (ATT) identified in the CFTR gene, exon 10, it results in the loss of a single amino acid phenylalanine at position 508 of the protein. This mutation is called DF508; “D” stands for deletion and “F” for phenylalanine amino acid.
1.Movement.
All living things move in some way.
2.Respiration is a chemical reaction that happens within cells to release energy from food.
3.Sensitivity.
The ability to detect changes in the surrounding environment.
4. Growth.
5.Reproduction.
Excretion
6. Nutrition.
Answer: The probability of getting a short winged fruit fly in the F1 generation is 2/4 or 1/2.
Explanation:
By using a monohybrid punnett square you should be able to come to the same answer.
