Answer: All the statements of the question are correct.
Sickle cell disease is an autosomal recessive disorder that is characterized by formation of defective hemoglobin protein, which results in sickle shaped RBC ( red blood cell).
This disease is caused by mutation in the gene that is responsible for the protein hemoglobin ( which transport oxygen throughout body).
It is inherited by the offspring when both the mutated copy of genes ( one from each parent) are passed to him.
Carriers of the disease exhibit increased resistance to malarial parasites by controlling the level of free haem in the blood ( through enzyme heme oxygenase that produces a toxic carbon monoxide gas). The resistance thus developed, is a mutation.
Therefore, all the statements in the given question are correct.
Answer:
it mostly controls all activites
Explanation:
the cell is main structural and functional unit of life in an animal body so without an animal cell the body won't function at all
D. a viral disease because it is known and unknown and spreads.
Answer:
The correct answer is the third option- the large ribosomal unit.
Explanation:
The translation is the second process of the protein synthesis in which transcribed mRNA molecule and transfer RNA or tRNA and ribosomes assemble together and complete synthesis of peptide chain or protein.
The assembly of initiator tRNA to ribosome subunits at the start codon of the mRNA is the initiation complex of the translation. The initiator tRNA is basically a met-tRNA molecule.
The initiator tRNA is bound to small subunit (30S) at 5' cap and scan for the start codon of mRNA.
Start codon bind to initiator RNA and in the end larger ribosomal unit assemble to this complex to complete the initiation complex of translation.
Thus, the correct answer is option - the large ribosomal subunit
