20 POINTS The following question has two parts. First, answer Part A. Then, answer Part B.

Caused by a mutation, sickle cell anemia is a disorder that affects hemoglobin, the red blood cell molecule that carries oxygen to cells throughout the body. The β chain of the hemoglobin protein is a single chain of amino acids and is 147 amino acids long. In humans, the gene that encodes for the β chain is located on chromosome 11. The diagrams show the DNA, RNA, and amino acid sequence of an unaffected person and a person with sickle cell anemia.

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Part A:

Where does the mutation that causes this disorder occur?

A
The mutation occurs on the DNA.

B
The mutation occurs on the RNA.

C
The mutation occurs on the ribosomes.

D
The mutation occurs on the amino acid.

Part B:

Which BEST describes the result of this mutation?

A
The entire sequence of amino acids is changed.

B
The RNA strand does not code for the correct amino acids.

C
The change in amino acids shortens the polypeptide sequence.

D
The alternation of a single nucleotide encodes for a different amino acid.

transcription is a process in which information is rewritten. it is something our cells must do, in a more specialized and narrowly defined way. in biology, transcription is the process of copying out the dna sequence of a gene in the similar alphabet of rna. it needs to happen in the nucleus because that's where the dna is. dna is always inside the nucleus unless the cell is dividing.

transcription is the first step in gene expression, which involves copying a gene's dna sequence to make an rna molecule. transcription is performed by rna polymerases. it has three stages: initiation, elongation, and termination. rna molecules must be processed after transcription in eukaryotes.

explanation:

long version:

the protein synthesis consists two processes which are, transcription and translation. transcription takes place in the nucleus. it uses dna as a template to make an rna molecule. rna then leaves the nucleus and goes to a ribosome in the cytoplasm, where translation occurs. transcription is the first part of the central dogma of molecular biology: dna → rna. it is the transfer of genetic instructions in dna to messenger rna (mrna). during transcription, a strand of mrna is made that is complementary to a strand of dna.  

these three stages are:

  initiation: in which   is the beginning of transcription.occuring when the enzyme rna polymerase binds to a region of a gene called the promoter. this signals the dna to unwind so the enzyme can ‘‘read’’ the bases in one of the dna strands. the enzyme is now ready to make a strand of mrna with a complementary sequence of bases.

    elongation: in which is the addition of nucleotides to the mrna strand. rna polymerase reads the unwound dna strand and builds the mrna molecule, using complementary base pairs. there is a brief time during this process when the newly formed rna is bound to the unwound dna. during this process, an adenine (a) in the dna binds to an uracil (u) in the rna.

    termination: in which is the ending of transcription, and occurs when rna polymerase crosses a stop (termination) sequence in the gene. the mrna strand is complete, and it detaches from dna.

nucleic acid molecules are incredibly complex, containing the code that guarantees the four different nucleotide units comprise dna, the nucleic acid of interest to the genealogist. and one of four nitrogen-containing molecules called nucleotides

sorry to break it to ya but no one can answer your question it's just

jk but i am serious about the part that most people cant answer it beacuse you did not mention the section you are talking about. but it would if you added some detail and were a bit more specific.