Dna replication

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[[DNA|DNA]] replication is a process where a complementary new DNA strand was synthesised from a template DNA strand.
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[DNA] replication is the process of copying a DNA molecule to produce two identical copies. This is the main method of transmitting parental characteristics to progeny.
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DNA replication is [semi conservative], as proposed by [Watson and Crick] in 1953. This means that the parental [DNA] unwinds to give two strands, each of which is then used as a [template] to synthesis a new [complementary strand]. Thus in each new DNA molecule, one strand is the conserved parental strand and the other is the new complement.
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The replication process is a complex enzyme catalysed mechanism with the involvement of associated proteins and RNA. It varies in [prokaryotes] and [eukaryotes] but the main mechanism remains analogous.
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Replication initiation begins at specific sites within the DNA called [origin of replication]. Circular prokaryotic DNA have one origin of replication while linear eukaryotic DNA have multiple origins. The origin of replication has protein binding sites to which an[ initiator protein] can bind. This protein recruits another enzyme called [helicase] and a special group of proteins called single [stranded DNA binding proteins]. The initiator protein also uses [ATP] to unwind the DNA slightly.
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The helicase binds to the unwound DNA and continues to unwind further and moves the replication fork along. As the helicase unwinds, the separated strands are prevented from rewinding by the [single stranded binding proteins].
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Next, the [enzyme] [primase] synthesises a short sequence of RNA [primer] complementary to the template. At the [3’ end] of the [leading strand] which runs 3’ to 5’. This primer is used as the starting point for [DNA polymerase III] to begin forming the complementary DNA strand in the 5’ to 3’ direction.
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The [lagging strand] runs in the 5’ to 3’ direction so the [complementary strand] has to run in the 3’ to 5’ direction. However, since DNA polymerase III can only add new [nucleotides] to the 3’ hydroxyl group of the previous nucleotide it can only synthesise strands in the 5’ to 3’ direction so synthesis on of a complement for the lagging strand is discontinuous.
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For this reason, multiple primers need to be formed on the lagging strand so DNA polymerase can synthesize in the 5’ to 3’ direction from every primer. These fragments of DNA are called [Okazaki fragments].
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Following polymerase III, another enzyme called [polymerase I] with [5’ to 3’ exonuclease activity], begins to remove the primers by replacing the [ribonucleotides] with [deoxyribonucleotides]. On the complement of the lagging strand, the fragments of DNA sequence are linked together by [DNA ligase].
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In eukaryotes, the end of replication is marked by the action of an enzyme [telomerase] which forms [telomeres] at the ends of the new DNA molecules.
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References:

Revision as of 21:21, 27 November 2014

[DNA] replication is the process of copying a DNA molecule to produce two identical copies. This is the main method of transmitting parental characteristics to progeny.

DNA replication is [semi conservative], as proposed by [Watson and Crick] in 1953. This means that the parental [DNA] unwinds to give two strands, each of which is then used as a [template] to synthesis a new [complementary strand]. Thus in each new DNA molecule, one strand is the conserved parental strand and the other is the new complement.

The replication process is a complex enzyme catalysed mechanism with the involvement of associated proteins and RNA. It varies in [prokaryotes] and [eukaryotes] but the main mechanism remains analogous.

Replication initiation begins at specific sites within the DNA called [origin of replication]. Circular prokaryotic DNA have one origin of replication while linear eukaryotic DNA have multiple origins. The origin of replication has protein binding sites to which an[ initiator protein] can bind. This protein recruits another enzyme called [helicase] and a special group of proteins called single [stranded DNA binding proteins]. The initiator protein also uses [ATP] to unwind the DNA slightly.

The helicase binds to the unwound DNA and continues to unwind further and moves the replication fork along. As the helicase unwinds, the separated strands are prevented from rewinding by the [single stranded binding proteins]. Next, the [enzyme] [primase] synthesises a short sequence of RNA [primer] complementary to the template. At the [3’ end] of the [leading strand] which runs 3’ to 5’. This primer is used as the starting point for [DNA polymerase III] to begin forming the complementary DNA strand in the 5’ to 3’ direction.

The [lagging strand] runs in the 5’ to 3’ direction so the [complementary strand] has to run in the 3’ to 5’ direction. However, since DNA polymerase III can only add new [nucleotides] to the 3’ hydroxyl group of the previous nucleotide it can only synthesise strands in the 5’ to 3’ direction so synthesis on of a complement for the lagging strand is discontinuous. For this reason, multiple primers need to be formed on the lagging strand so DNA polymerase can synthesize in the 5’ to 3’ direction from every primer. These fragments of DNA are called [Okazaki fragments].

Following polymerase III, another enzyme called [polymerase I] with [5’ to 3’ exonuclease activity], begins to remove the primers by replacing the [ribonucleotides] with [deoxyribonucleotides]. On the complement of the lagging strand, the fragments of DNA sequence are linked together by [DNA ligase].

In eukaryotes, the end of replication is marked by the action of an enzyme [telomerase] which forms [telomeres] at the ends of the new DNA molecules.

References:

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