Replication and Recombination

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28 Terms

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dna ligase

An enzyme that facilitates the joining of DNA strands together by forming phosphodiester bonds. It plays a crucial role in DNA replication and repair, sealing nicks in the sugar-phosphate backbone.

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<p>replication</p>

replication

The biological process of copying DNA to produce two identical DNA molecules, essential for cell division.

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translesion synthesis

A DNA damage tolerance process that allows the DNA replication machinery to synthesize DNA over a lesion or damaged region, enabling the continuation of replication despite the presence of DNA damage.

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primase

An enzyme that synthesizes short RNA primers necessary for DNA replication. Primase provides a starting point for DNA polymerase to begin synthesis of the new DNA strand.

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proofreading

A critical process during DNA replication that corrects errors by removing and replacing incorrectly paired nucleotides, ensuring high fidelity in DNA synthesis.

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okazaki fragment

Short segments of DNA synthesized on the lagging strand during DNA replication. They are later joined together by DNA ligase to form a continuous strand.

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ligation

The process of joining two DNA fragments together, typically performed by the enzyme DNA ligase, which seals the sugar-phosphate backbone of the DNA.

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<p>replication bubble</p>

replication bubble

The structure formed when DNA unwinds and separates during the process of DNA replication, allowing for the simultaneous synthesis of new DNA strands.

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<p>replication fork</p>

replication fork

The Y-shaped structure that forms at the junction where the double-stranded DNA separates into two single strands during DNA replication, allowing for new strand synthesis.

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continous

DNA synthesis that occurs in the same direction as the replication fork, resulting in a continuous strand of DNA being formed.

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discontinuous

DNA synthesis that occurs in the opposite direction to the replication fork, resulting in the formation of short segments called Okazaki fragments.

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helicase

An enzyme that unwinds the DNA double helix at the replication fork, separating the two strands to allow for replication.

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<p>crossing over</p>

crossing over

A process during meiosis where homologous chromosomes exchange genetic material, leading to genetic diversity in gametes.

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branch migration

the process where recombined homologous chromosomes move apart, allowing for the exchange of genetic material to be extended along the length of the chromosomes.

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<p>leading strand</p>

leading strand

the leading strand is the DNA strand that is synthesized continuously during replication in the 5' to 3' direction, allowing for rapid copying of the template strand.

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<p>lagging strand</p>

lagging strand

the lagging strand is the DNA strand that is synthesized discontinuously during replication in short segments called Okazaki fragments, which are later joined together, allowing it to be copied in the 5' to 3' direction.

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origin of replication

the origin of replication is the specific site on a DNA molecule where replication begins, marked by the unwinding of the double helix and the assembly of the necessary proteins and enzymes for DNA synthesis.

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initiator protein

a protein that binds to the origin of replication to initiate the process of DNA replication by unwinding the double helix and recruiting additional enzymes.

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primer

a short single-stranded nucleic acid sequence that provides a starting point for DNA synthesis during replication, allowing DNA polymerase to begin the addition of nucleotides.

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strand displacement

a mechanism during DNA replication where a newly synthesized strand displaces an existing strand, allowing for the formation of a new double helix.

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resolution

the process of separating the two daughter DNA molecules after replication, ensuring that each new DNA molecule is complete and intact.

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5’-3’ polymerase activity

refers to the ability of DNA polymerase to synthesize a new DNA strand by adding nucleotides in the 5’ to 3’ direction, which is essential for DNA replication.

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3’-5’ exonuclease activity

is a proofreading function of DNA polymerase that allows it to remove incorrectly paired nucleotides from the newly synthesized DNA strand, enhancing the fidelity of DNA replication.

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5’-3’ exonuclease activity

is a function of DNA polymerase that allows the enzyme to remove nucleotides from the RNA primer or from the newly synthesized DNA strand, facilitating the removal of primers during replication.

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telomere

is a repetitive nucleotide sequence at the ends of chromosomes that protects them from deterioration or fusion with neighboring chromosomes, playing a crucial role in chromosome stability.

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<p>telomerase </p>

telomerase

is an enzyme that adds repetitive nucleotide sequences to the ends of telomeres, thereby extending their length and helping to maintain chromosome stability during cell division.

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<p>holliday junction</p>

holliday junction

is a crucial intermediate structure formed during homologous recombination, characterized by the crossover of two double-stranded DNA molecules, facilitating genetic exchange.

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<p>heteroduplex</p>

heteroduplex

is a DNA molecule formed from strands of different origins during homologous recombination, often resulting in genetic variations.