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Difference Between Replication And Transcription

DNA serves as the molecular basis of heredity whereas Replication creates identical DNA strands. Check this article to know more about the Difference Between Replication And Transcription.
authorImageJasdeep Bhatia16 Mar, 2024
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Difference Between Replication And Transcription

Difference Between Replication And Transcription: DNA replication is the procedure used to produce two daughter strands, each comprising half of the DNA double helix. During the S phase of the cell cycle, this takes place. DNA Helicase and DNA Polymerase are the enzymes involved in this process.

On the other hand, transcription is the procedure used to convert genetic data from DNA to RNA. The cell's G1 and G2 stages are where this process takes place. RNA polymerase is its catalyser. Check out this post to see how they vary from one another.

Introduction

Complementary nucleotides must bind to DNA during DNA replication and transcription to produce new DNA and RNA strands. DNA replicates to create two identical copies of the entire genome for cell division. Transcription, on the other hand, is the initial stage of gene expression, which results in the production of crucial proteins for cell function. Transcription only produces RNA from brief DNA sequences. The main difference between transcription and DNA replication is that the former entails making an exact genome copy. In contrast, the latter entails converting the genetic material of a particular DNA segment into RNA.

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DNA Replication

The process of making two identical copies of one DNA molecule is known as DNA replication. In DNA replication, the genetic information kept in the DNA is passed down through the progeny. Both DNA strands act as templates for replication. As a result, it is believed that DNA replication takes place in a semiconservative way. Each chromosome's origin of replication is where DNA replication begins. The DNA polymerases enzyme family is responsible for the process. A short strand of RNA known as a primer is needed for DNA polymerase to start the replication process. The genome's double helix unwinding creates the replication forks. Several enzymes are connected to the replication at the replication fork. At the replication fork, DNA replication happens in both directions.

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The leading strand is the term used to describe the constantly synthesised new DNA strand. The other strand, known as the lagging strand, is composed of bits known as Okazaki fragments. By incorporating nucleotides that are complementary to the template, DNA polymerase creates the new strand. Starting at the 3′ ends of the preexisting nucleotide chain, nucleotides are added in the 3′ to 5′ direction. The phosphodiester link between the proximal phosphate group and the 3′ OH of the pentose ring of the entering nucleotide creates the sugar-phosphate backbone. The additional enzymes involved in DNA replication are topoisomerase, helicase, DNA primase, and DNA ligase. The telomeric regions of chromosomes are where DNA replication comes to an end. Because the mismatch incorporation rate is less than 1 per 107 integrated nucleotides, DNA polymerases frequently maintain excellent fidelity. Additionally, students offer a 3 to 5-foot proofreading exercise where they can correct any end-to-integrated inconsistencies. On the other hand, mismatches can be corrected by post-replication mismatch repair mechanisms. The final incorporation rate is less than one error per 109 integrated nucleotides. DNA is replicated in vitro using synthetic DNA primers and DNA polymerases derived from bacteria. The polymerase chain reaction is the name of the molecular biological technique used for in vitro DNA replication (PCR). Taq polymerase is the name of the enzyme utilised in PCR. In PCR, DNA primer pairs are commonly used to separate DNA fragments from a known sequence.

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Transcription

By using the enzyme RNA polymerase, a DNA sequence is copied into RNA during transcription. To start the gene expression, genes are translated into mRNAs. By reading the antisense DNA strand from 3′ to 5′, RNA polymerase synthesises the mRNA main transcript. The resultant strand of RNA is antiparallel and complementary to the template. It is synthesised in the direction of 5′ to 3′. Coding sequences and regulatory sequences are both parts of a gene. While regulatory sequences control the expression of genes, coding sequences encode the amino acid sequence of a protein. With the help of transcription factors, RNA polymerase binds to the promoter to begin transcription. The unwinding double-stranded promoter's approximately 14 bases make up the transcription bubble created by the binding. Nucleotides are added by RNA polymerase after the transcription initiation site is chosen. The 3′ ends of the main transcript are appended to a polyadenylated tail at the point where the transcription ends.

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Post-transcriptional alterations refer to the splicing of exons, polyadenylation, and 5′ end capping in eukaryotes. Genes can also produce non-coding RNAs, rRNAs, and tRNAs, essential for synthesising, regulating, and processing proteins.

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Difference Between Replication And Transcription

Replication Transcription
Two identical copies of the original double-stranded DNA molecule is created via DNA replication. One original DNA strand makes up each of the new strands. Using double-stranded DNA, transcription creates a single-stranded RNA molecule.
It passes on its full DNA to its progeny. It produces RNA copies of a certain gene.
Enzymes are DNA primase, DNA ligase, topoisomerase, and helicase. Enzymes are RNA polymerase and transcriptase, a form of DNA helicase.
It takes place as the cell prepares to divide during the S phase. The cell must synthesise proteins in the G1 and G2 phases.
Hydrogen bonds hold a newly synthesised DNA strand to its template. Transcripted RNA emerges from its template.
An RNA primer is needed by DNA polymerase to start the replication process. Primers are not needed for RNA polymerase.
The lagging strand produces pieces of Okazaki. Except the Okazaki fragments, transcription only happens in the 5′ to 3′ direction.
There are two daughter strands created. The production of mRNA, tRNA, rRNA, and non-coding RNA like microRNA.
In the nucleus, same DNA is still there. A larger portion of the product enters the cytoplasm.
Through progeny, replicated DNA is conserved. Even before they start to work, the majority of RNAs are destroyed.
DNA that has just been created gets unprocessed. Post-transcriptional changes are made to transcribe RNAs.

Difference Between Replication And Transcription <span style=

Why does DNA replication occur?

For DNA replication to begin, there are two processes. A protein known as an initiator initially unravels a short section of the DNA double helix before unraveling the remaining portion. When the helicase protein breaks the hydrogen bonds between the bases on the DNA strands, the two strands of DNA are forced apart.

What function does DNA replication serve before cell division?

A double-stranded DNA molecule is split into two identical DNA molecules during DNA replication. Because every time a cell splits, the two new daughter cells must have the same genetic material, or DNA, as the parent cell, replication is crucial.

Where do transcription and replication take place?

Translation takes place in the cytoplasm, whereas replication and transcription take place in the nucleus.

What enzyme is involved in transcription and replication?

The primary enzyme required for replication is DNA polymerase. A section of DNA is used as a template during transcription to create an RNA sequence. RNA polymerase is the primary enzyme responsible for the transcription. mRNA, rRNA, and tRNA are the three forms of RNA that are created during transcription.

What is the best way to stop transcription?

Until it receives a signal to stop, RNA polymerase will keep on transcription. The final step in the transcription process is called termination, which occurs when the polymerase transcribes a terminator sequence of DNA.
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