D1 Continuity and Change : Molecules Flashcards

DNA replication, protein synthesis and mutations

1
Q

histones

A

Proteins around which eukaryotic DNA is wrapped, forming structures called nucleosomes. This organisation helps to regulate gene expression and protect the structural integrity of DNA.

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2
Q

nucleosomes

A

A structural unit of eukaryotic chromatin, consisting of DNA wrapped around a core of histone proteins.§

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3
Q

helicase

A

An enzyme that unwinds and separates the DNA double helix during DNA replication.

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4
Q

polymerase chain reaction (PCR)

A

A laboratory technique used to amplify a specific DNA sequence, producing multiple copies of it.

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5
Q

primers

A

A short DNA or RNA sequence that serves as a starting point for DNA synthesis by DNA polymerase.

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6
Q

taq polymerase

A

A heat-stable DNA polymerase commonly used in PCR reactions.

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7
Q

3 phases of taq polymerase

A
  • denaturation = DNA heated + strands separate
  • annealing = temp lowered so primers can bind to complementary sequences on DNA template
  • extension = DNA polymerase extends the primers by synthesising new DNA strands
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8
Q

gel electrophoresis

A

A technique used to separate and analyse DNA fragments based on their size and charge using an electric field and a gel matrix.

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9
Q

phosphodeister bonds

A

The covalent bond that forms between the phosphate group of one nucleotide and the sugar of the adjacent nucleotide in a DNA or RNA strand.

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10
Q

replication fork

A

The Y-shaped structure formed during DNA replication where the DNA double helix is unwound and new strands are synthesised.

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11
Q

leading strand

A

The DNA strand that is synthesised continuously in the 5ʹ to 3ʹ direction during DNA replication.

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12
Q

lagging strand

A

The DNA strand that is synthesised discontinuously in short fragments called Okazaki fragments during DNA replication.

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13
Q

okazaki fragments

A

Short DNA fragments that are synthesised on the lagging strand during DNA replication and later joined together.

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14
Q

DNA primase

A

An enzyme that synthesises short RNA primers needed for DNA replication.

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15
Q

DNA Polymerase I

A

An enzyme involved in DNA repair that removes RNA primers and replaces them with DNA.

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16
Q

DNA polymerase III

A

The primary DNA polymerase responsible for DNA synthesis during replication in prokaryotic cells.

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17
Q

DNA ligase

A

An enzyme that catalyses the joining of DNA fragments by forming phosphodiester bonds between them.

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18
Q

single strand binding proteins

A

Proteins that bind to and stabilise single-stranded DNA during DNA replication or repair.

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19
Q

gyrase

A

An enzyme involved in DNA replication that helps relieve the tension and supercoiling generated ahead of the replication fork.

20
Q

transcription

A

Process by which the genetic information encoded in DNA is copied into RNA.

21
Q

mRNA§

A

Messenger RNA, a type of RNA that carries the genetic information from DNA in the nucleus to ribosomes in the cytoplasm, where it is used as a template to synthesise proteins.

22
Q

translation

A

Process by which ribosomes use the genetic information carried by mRNA to synthesise proteins.

23
Q

tRNA

A

A type of RNA molecule that acts as an adaptor during translation, bringing amino acids to the ribosome and aligning them in the correct order based on the mRNA sequence.

24
Q

codon

A

A set of three adjacent nucleotides in DNA or mRNA that code for a particular amino acid.

25
Q

anticodon

A

A sequence of three nucleotides in tRNA that is complementary to a specific codon in mRNA, allowing the tRNA to recognise and bind to the corresponding codon.

26
Q

degeneracy

A

Refers to the redundancy in the genetic code, which allows for multiple codons to code for the same amino acid.

27
Q

3 types of mutations

A

frameshift
- insertion
- deletion
substitution

28
Q

introns

A

Non-coding regions or intervening sequences within a gene that are transcribed into RNA but are removed during post-transcriptional processing.

29
Q

telomere

A

Repeated nucleotide sequences located at the ends of chromosomes that protect the genetic information from degradation and maintain chromosome stability during DNA replication.

30
Q

exons

A

Coding regions within a gene that contain the instructions for synthesising a protein and are retained in the mature RNA molecule.

31
Q

pre-mRNA

A

The initial RNA molecule transcribed from DNA, which contains both introns and exons.

32
Q

a 5’ cap

A

A modified guanine nucleotide added to the 5’ end of pre-mRNA during post-transcriptional modification, providing stability and assisting in mRNA processing and transport.

33
Q

poly-A tail

A

Multiple adenine nucleotides added to the 3´ end of a mRNA transcript to protect and stabilise the molecule.

34
Q

splicing

A

The process of removing introns from pre-mRNA and joining the exons together to produce mature mRNA that can be translated into a protein.

35
Q

3 stages of translation

A
  • initiation = ribosome assembles and starts new chain
  • elongation = adding amino acids
  • termination = ribosome recognises a stop codon and releases chain
36
Q

single nucleotide polymorphisms (SNPs)

A

Replacement of a single nucleotide with another, producing variation within a species. These are often found in non-coding regions of DNA

37
Q

synonymous substitutions

A

A neutral mutation that does not change the amino acid sequence due to the degeneracy of the genetic code.

38
Q

non-synonymous substitutions

A

A mutation that causes a change in the amino acid sequence.

39
Q

mutagens

A

Agents that can cause mutations.

40
Q

3 chemical mutagens

A
  • mustard gas
  • nitrous acid
  • formaldehyde
41
Q

3 effects of mutations

A
  • beneficial
  • harmful
  • silent
42
Q

genetic engineering

A

The process of altering the DNA of an organism in order to introduce new characteristics, remove unwanted traits or modify existing ones.

43
Q

gene knockout

A

A technique in which a specific gene is intentionally made inoperative to study its function.

44
Q

CRISPR

A

A specific region of DNA that is found in bacteria that contains short, repeated sequences and unique spacer sequences that are incorporated from foreign DNA encountered by the bacteria.

45
Q

cas9

A

An endonuclease enzyme that can be used to cut DNA at specific target sites on a chromosome.