topic 7 : modern genetics Flashcards

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1
Q

what is a genome

A

all of the DNA of an organism including mitochondrial/chloroplast DNA

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2
Q

what is the PCR used for

A

amplify DNA sample. used for dna sequencing and dna profiling

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3
Q

what is DNA sequencing

A

determine nucleotide sequence

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4
Q

what is DNA profiling

A

identifies unique sections of DNA to identify an individual

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5
Q

How is PCR done

A
  1. Reaction mixture contains: DNA sample, primers (short section of complementary DNA, its used as a starting point for the free nucleotides to then continue making the complementary chain), free nucleotides, Taq DNA polymerase (taken from organisms living in extreme heat environments so that the enzyme does not denature at high temp)
  2. The mixture is heated 99C to break the H bonds between the complementary bases of the DNA (DNA unzips)
  3. The mixture is then cooled 55C to allow the primers to join to the complementary section of the DNA – annealing
  4. Mixture is heated again to 70C (optimum temp for Taq polymerase) for the phosphodiester bonds to form between the free nucleotides
  5. This is repeated several times to produce many molecules of the DNA sample
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6
Q

why is DNA sequencing used

A

used to predict the amino acid sequence and to determine the links between genetically connected individuals. This is done by gel electrophoresis

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7
Q

How is DNA sequencing done

A
  1. The sample of DNA is divided into four separate sequencing reactions. Each of the reactions contain the 4 standard nucleotides, DNA polymerase, primers and fluorescently labelled terminator nucleotides
  2. The primers initiate the formation of complementary strands
  3. Terminator nucleotides cause the replication to be terminated
  4. As a result, several fragments of complementary strands are produced which are all different in size
  5. Gel electrophoresis is used to separate the fragments
  6. Fragments are viewed under UV light to enable the base sequence to be read
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8
Q

what is DNA profiling used for

A

used for forensics to identify individuals and paternity testing

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9
Q

how is dna profiling done

A
  1. Fragments of DNA are cut by restriction enzymes
  2. The fragments are separated using gel electrophoresis
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10
Q

how is gel electrophoresis done

A
  1. Fragments of DNA are placed in agar, and they are dyed with ethidium bromide so they are visible under UV light
  2. DNA is negatively charged so it moves and is attracted towards the positive electrode at the end of the electrophoresis equipment
  3. Fragments of DNA have different masses, so the lighter fragments move quicker and the heavier fragments move slower
  4. This produces the appearance of various “bands” which can be analysed to identify the DNA sequence
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11
Q

what is gene expression

A

The process by which a gene gets turned on in a cell to make RNA and proteins.

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12
Q

what are transcription factors

A

proteins which bind to specific base sequences on DNA
- they sometimes initiate protein synthesis and other times they prevent protein synthesis

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13
Q

what are promotor sequences

A
  1. They are found upstream of the gene they act on
  2. Enable the binding of RNA polymerase and hence promotes transcription
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14
Q

what are enhancer sequences

A
  1. Regulate DNA structure by changing the structure of chromatin
  2. This allows/prevent RNA polymerase from binding
  3. Open: gene expression is active, Closed: gene expression is inactive
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15
Q

what is epigenetics

A

heritable and reversible modifications to the DNA that do not involve changes to the nucleotide sequence.

  1. Study of changes in organisms due to the changes in gene expression rather than the change in the actual DNA code
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16
Q

what is DNA methylation

A

when a Ch3 group is added to a CpG site (cytosine next to a guanine) on DNA. It prevents transcription and it has an effect on histone structure to make the DNA more/less accessible to RNA polymerase

17
Q

what is a histone protein

A

type of protein found in chromosomes. Histones bind to DNA, help give chromosomes their shape, and help control the activity of genes.

18
Q

what is histone modification

A
  1. Methylation to cause the activation/inactivation of transcription
  2. Acetylation: addition of a COCH3 group which allows transcription
19
Q

what is non-coding RNA

A

does not code for amino acids, but instead affects transcription or modifies the products of transcription

  1. E.g. ncRNA coats an X chromosome which causes it to super coil and condense to become stable and inactive Barr body – this maintains the balance the products of genes
20
Q

what is RNA splicing

A
  1. After transcription, the mRNA produced is immature: pre mRNA
  2. Introns (non coding regions) are removed
  3. The exons (coding regions) are joined together by an enzymes called spliceosomes
  4. Mature mRNA is produced