Because DNA Polymerase requires the OH on the 3' as an active site. It uses the OH on the 3' end of a nucleotide to attach a phosphate from the 5' end of the next nucleotide. It only works in this direction, and that is why DNA polymerase works 5' to 3'.
DNA polymerase requires a primer to initiate the synthesis of new DNA strands because it can only add nucleotides onto an existing strand of DNA. The primer provides a starting point for the polymerase to begin adding nucleotides and building the new DNA strand.
RNA primase is used to synthesize short RNA primers that are needed for DNA replication by DNA polymerase. This RNA primer can be easily replaced by DNA once DNA polymerase starts synthesizing the new DNA strand. This is different from DNA primase which synthesizes RNA primers during the synthesis of Okazaki fragments on the lagging strand during DNA replication in prokaryotes and eukaryotes.
The enzyme responsible for extending the new DNA strand by adding nucleotides is DNA polymerase. It reads the template strand and adds complementary nucleotides to form a new DNA strand. DNA polymerase can only add nucleotides in the 5' to 3' direction.
During DNA duplication, an RNA primer is used because DNA polymerase can only add new nucleotides to an existing nucleic acid strand rather than initiating synthesis. The RNA primer provides a starting point for DNA polymerase to bind and begin adding complementary nucleotides to synthesize a new DNA strand. This primer is later removed and replaced with DNA nucleotides to complete the replication process.
RNA polymerase attaches to unwound DNA during transcription by recognizing and binding to specific promoter sequences on the DNA strand. Once bound, the RNA polymerase begins to synthesize a complementary RNA strand using the DNA template.
A primer molecule is required for DNA polymerase to initiate the addition of nucleotides. This primer provides a starting point for DNA polymerase to begin adding nucleotides in the correct sequence. Once the primer is in place, DNA polymerase can add nucleotides complementary to the template strand.
DNA polymerase requires a primer to initiate the synthesis of new DNA strands because it can only add nucleotides onto an existing strand of DNA. The primer provides a starting point for the polymerase to begin adding nucleotides and building the new DNA strand.
A primer (oligonucleotide of a specific sequence) is required for Taq polymerase to extend the template strand by adding complementary nucleotides. The function of the primer is to anneal to the template strand at a very specific site and facilitate the initiation of strand elongation mediated by Taqploymerase.
RNA primase is used to synthesize short RNA primers that are needed for DNA replication by DNA polymerase. This RNA primer can be easily replaced by DNA once DNA polymerase starts synthesizing the new DNA strand. This is different from DNA primase which synthesizes RNA primers during the synthesis of Okazaki fragments on the lagging strand during DNA replication in prokaryotes and eukaryotes.
No, initiation of transcription does not require a primer. Transcription begins at the promoter region of a gene, where RNA polymerase binds and starts synthesizing a complementary RNA strand using the template DNA strand. In contrast, DNA replication requires a primer to initiate synthesis.
The enzyme responsible for extending the new DNA strand by adding nucleotides is DNA polymerase. It reads the template strand and adds complementary nucleotides to form a new DNA strand. DNA polymerase can only add nucleotides in the 5' to 3' direction.
With a small piece of primer,and active polymerase(enzyme) it replicates the complementary strand of the DNA
During DNA duplication, an RNA primer is used because DNA polymerase can only add new nucleotides to an existing nucleic acid strand rather than initiating synthesis. The RNA primer provides a starting point for DNA polymerase to bind and begin adding complementary nucleotides to synthesize a new DNA strand. This primer is later removed and replaced with DNA nucleotides to complete the replication process.
DNA polymerase is an enzyme that helps to make new matching DNA strand by adding nucleotides one at a time and joining each new nucleotide to the previous nuEach new nucleotidecleotide in the growing DNA strand.
RNA polymerase attaches to unwound DNA during transcription by recognizing and binding to specific promoter sequences on the DNA strand. Once bound, the RNA polymerase begins to synthesize a complementary RNA strand using the DNA template.
DNA polymerase cannot begin the synthesis of new DNA.To synthesis a new strand of DNA ,RNA primer is required.The complementary RNA nucleotides,that are added opposite to the single strand of parent DNA are the RNA primer.
For DNA polymerase to link nucleotides together, the first nucleotide must be attached to a primer, which is a short segment of RNA or DNA that provides a free 3' hydroxyl group for the DNA polymerase to start adding nucleotides. DNA polymerase can only extend nucleotides from an existing primer or strand, using it as a template for complementary base pairing.