The RNA base sequence will be CGAUUAGGC
This answer assumes that the DNA sequence in the question is the sequence on the template strand.
The way to work it out is to take the complementary base of each base in the DNA:
the complement of G is C
the complement of C is G
the complement of A is U in RNA (T in DNA)
the complement of T is A
Answer is actually (E) ATACA because if you use TATGA and do the complement, which is a=t and c=g
Incorrect nucleotides added during DNA replication can be repaired by enzymes that detect and remove the mismatched nucleotides, a process known as mismatch repair. This mechanism helps maintain the accuracy of the DNA sequence.
DNA replication is a semi-conservative process. The DNA is split into two strands. Nucleotides are then attached to each strand by complementary base pairing, where A attaches to T and G attaches to C. The newly formed strand is hence identical to the old strand and the base sequence of DNA can hence be conserved during replication.
The arrangement of nucleotides in DNA determines the sequence of amino acids in a protein through the process of transcription and translation. During transcription, RNA is synthesized from DNA, and during translation, the sequence of RNA nucleotides is decoded into a specific sequence of amino acids, forming a protein specified by the DNA sequence.
DNA Polymerase is the enzyme which adds new nucleotides during replication.
DNA polymerase is the enzyme responsible for assembling complementary nucleotide bases during DNA replication. It adds new nucleotides to the growing DNA strand based on the template strand.
Incorrect nucleotides added during DNA replication can be repaired by enzymes that detect and remove the mismatched nucleotides, a process known as mismatch repair. This mechanism helps maintain the accuracy of the DNA sequence.
DNA polymerase is the enzyme responsible for connecting nucleotides together during DNA replication. It adds complementary nucleotides to the newly synthesized DNA strand.
True. DNA polymerase enzymes are responsible for adding nucleotides to synthesize a new DNA strand during replication, ensuring that the correct base sequence is maintained.
The DNA segment ttacgc would pair with the complementary RNA sequence aaugcg during replication. In RNA, adenine (A) pairs with uracil (U) instead of thymine (T).
DNA replication is a semi-conservative process. The DNA is split into two strands. Nucleotides are then attached to each strand by complementary base pairing, where A attaches to T and G attaches to C. The newly formed strand is hence identical to the old strand and the base sequence of DNA can hence be conserved during replication.
The arrangement of nucleotides in DNA determines the sequence of amino acids in a protein through the process of transcription and translation. During transcription, RNA is synthesized from DNA, and during translation, the sequence of RNA nucleotides is decoded into a specific sequence of amino acids, forming a protein specified by the DNA sequence.
DNA polymerase is the enzyme responsible for positioning nucleotides during DNA replication. DNA polymerase can add nucleotides to the growing DNA strand in the 5' to 3' direction and proofread for errors in base pairing.
DNA Polymerase is the enzyme which adds new nucleotides during replication.
DNA polymerase is the enzyme responsible for assembling complementary nucleotide bases during DNA replication. It adds new nucleotides to the growing DNA strand based on the template strand.
Not necessarily. Mutations can result from a variety of changes to the DNA sequence, including substitutions, deletions, or insertions of nucleotides. These changes can be spontaneous errors during DNA replication, exposure to mutagens, or environmental factors.
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A change in the nucleotide sequence of DNA is called a mutation.Mutations take several forms:* substitution: one base is replaced by another* deletion: one or more nucleotides disappear from the sequence and the rest close up* insertion: one or more nucleotides appear between what had been adjacent nucleotides* duplication: a form of insertion in which a sequence of nucleotides is copied and now appears twice instead of once. Mutations can be caused by certain types of radiation, including ultraviolet (UV), and certain chemical compounds, which are therefore referred to as mutagenic.Mutations are particularly likely to occur at a point during replication of DNA when the two strands are separated.