Answer:
(A). Result in different amino acids to be read due to frame shifts
Explanation:
Insertion or deletion mutations (or Indel mutations) can be defined as mutations in DNA due to insertion (addition) or deletion of nucleotide bases in DNA.
These mutations lead to change in reading frames (sequence of codons), which leads to formation of protein having completely different amino acid sequence. Hence, these mutations are also cause frameshift mutations.
This is due due to triplet nature of genetic codes as insertion or deletion of one or more bases (but not three) would change change in codon sequence and mutated sequence can form a non-functional or truncated protein.
Thus, the correct answer is option (A).
<h3><u>Answer;</u></h3>
D) it lacks a nuclear membrane and resides inside the nucleus
<h3><u>Explanation;</u></h3>
- <em><u>Nucleolus is a type of cell organelle that is located in the nucleus of an tom. </u></em>Nucleus is the control center of an atom, it controls all the cellular activities taking place in the cell.
- <em><u>Nucleolus is made up of ribosomal RNA and proteins. The main function of the nucleolus is to assemble or formation of ribosomes. </u></em>Ribosomes are cell organelles that are found in the cytoplasm either attached on the endoplasmic reticulum or freely floating in the cytoplasm, where the process of protein synthesis takes place.
Answer:
the correct answer is 25%
Explanation:
the whole amount of squares is 100%. to get a homozygous dominant you must have two capital letters. only one box has two capital letters so that makes 25%
Answer:
The three genes in coupling are in repulsion.
Explanation:
Coupling happens when the dominant alleles and the recessive alleles are on the same homologous chromosome, while the repulsion happens when one chromosome has one dominant allele and one recessive allele and another homologous chromosome also has dominant and recessive alleles.
If the progeny has:
nb+ ls+ a/nb ls a ⇒ nb+ ls+ a
nb ls a+/nb ls a ⇒ nb ls a+
Where nb+ ls+ a is the dominant alleles and nb and nb+ is in middle.
ls+ nb+ are on the same chromosome (both dominant)
ls nb are on the same chromosome (both recessive)
ls nb, these two are in coupling with each other, but ls+ and a are on the chromosome and ls+ or nb+ are dominant, while nb+ and a are recessive on form a, thus, ls and nb, they are in repulsion with a.
B: receptor, sensory, interneuron, motor, effector
