Gene Expression Flashcards

1
Q

Universal

A

Same triplet codes for the same amnio acids in all organisms

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2
Q

Non overlapping

A

Each base is read once in a triplet

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3
Q

Degenerate

A

More than one triplet codes for each amino acid

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4
Q

3 types of mutagenic agents and examples and what they do

A
  1. High energy radiation which damage DNA molecule and chemicals alter DNA structure/ effect DNA replication= x rats, gamma rays
  2. DNA reactive chemicals= nitrous oxide removes a NH2 from cytosine converting it into uracil
  3. Biological Agents = Viruses and bacteria
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5
Q

Stem cell definition

A

They are undifferentiate that can divide into any type of cell continually and become specialised

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6
Q

4 types of stem cells

A

Pluripotent
Totipotent
Multipotent
Unipotent

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7
Q

Stem cell

A

Cells that can differentiate by mitosis into two genetically identical cells one remains of the stem cell on the other differentiate into a specialised cell by translating part of the DNA.

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8
Q

Totipotent

A

They can divide and differentiate into any type in cell and produce a whole new organism found up to 8 cell stages in early mammalian embryo for a limited time

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9
Q

Pluripotent

A

Divide unlimited times and differentiate into any type of cell found in an embryo

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10
Q

Multi potent

A

Divide a limited number of times and differentiate into a limited number of different type types of cell found in mature mammal tissues e.g. bone marrow

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11
Q

Uni potent

A

Divide a limited number of times and differentiate into one cell type found in hard as cardiomycocytes

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12
Q

Applicational stem cells to medical research

A
  1. Producing tissues for skin graft.
  2. Research introduce an organs for transplant.
  3. Research into how cells become specialised.
  4. Use of stem cells to cure diseases such as Parkinson’s disease.
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13
Q

Ethical concerns about using stem cells in IPC

A
  1. Not right to use stem cells from embryos as embryos are human.
  2. Embryos have no moral rights
  3. Donors consent.
  4. Animal testing.
  5. Cancer
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14
Q

Promoter region

A

One or more basic sequence is found before a gene that control the expression of that gene

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15
Q

Transcription factors

A

Proteins which when activated by to the promoter region of a gene stimulating RNA polymerase to begin transcription of that target gene

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16
Q

Oestrogen acting as a transcription factor

A
  1. Oestrogen diffuses through the phospholipid cell membrane as its lipid soluble.
  2. Diffuses through the nuclear envelope.
  3. Binds to the oestrogen receptor protein.
  4. Changes the tertiary structure.
  5. Releases the transcription factor.
  6. Transcription factor by to the DNA.
  7. At the promoter region.
  8. This allows stimulation of RNA to transcribe the gene.
  9. This increases transcription or mRNA is produced.
17
Q

How does interfering RNA work?

A
  1. Enzyme cuts mRNA into SI RNA.
  2. One strand of SI RNA combines with another enzyme.
  3. The sRNA enzyme complex will bind via complementary base pairing to named gene proteins mRNA.
  4. Once abound the enzyme will cut up the mRNA so it could no longer be transcribed or no ribosome can bind
  5. So reduction of translation of name protein.
  6. So reduces name protein in cell cell less name protein function.
18
Q

Why can’t some protein still be made even if there is interfering RNA

A

More mRNA has been transcribed and there is interfering RNA so not all mRNA is bound to RNAi
So not Emma, all of mRNA is destroyed

19
Q

Epigenetic definition

A

Heritable changes in gene function
Without changes to the base sequence of DNA

20
Q

What is methylation?

A

Addition of methyl groups added to DNA which tightens the DNA so no RNA polymerase can translate the DNA

21
Q

What is acetylation

A

Addition off acetal groups to histones proteins which results in them becoming loosely packed so DNA is less coiled

22
Q

Gene switched off

A

No translation or transcription

23
Q

Gene switched on

A

There is transcription and translation

24
Q

Describe and explain the epigenetic modification that keeps the gene switched off

A
  1. Increase methylation means name transcription factor cannot bind to promotor a region of DNA.
  2. Decrease acetylation of his protein tails results in DNA more tightly packed.
  3. Less expression of gene.
  4. So RNA polymerase cannot bind to DNA next promoter.
  5. So less mRNA of named gene produced
  6. So less named protein function.
25
Q

Describe and explain the Epigenetics modification that keep the genes turned on

A
  1. Decrease methylation means transcription factor binds to promote a region of DNA.
  2. Increased acetylation of his stone protein tales means DNA more loosely packed.
  3. More expression of gene.
  4. More RNA by a DNA promoter region.
  5. Scribes names protein producing more mRNA.
  6. More protein.
  7. More name protein function.
26
Q

Tumour suppressor gene

A

Genes that code for a protein that stops cell division

27
Q

Proto-oncogene

A

Gene that code for a protein that starts cell division

28
Q

Cancer

A

Uncontrolled rapid mitosis

29
Q

Tumour

A

Mass of abnormal cells from uncontrolled mitosis

30
Q

Malignant tumour

A

Cells that have metastasised and can spread around the body

31
Q

Benign tumours

A

Cells that are metastasised and will not spread around other parts of the body

32
Q

Does tumour suppressor gene need to be turned off or on?

A

No, a cell cycle needs to start

33
Q

Describe how tumor could form because of epigenetic modifications to Tumor suppressor genes

A
  1. More methylation of a suppressor gene DNA promoter region
  2. Less acetylation of histones proteins around humans oppressed genes.
  3. Less expression of named tumour suppressor gene.
  4. Less transcription of gene.
  5. Less mRNA formed.
  6. Less translation.
  7. Less named protein that stop cell cycle.
  8. Leads to uncontrolled cell division.
34
Q

Describe how humours could form because of epigenetic modifications to proto-oncogenes

A
  1. Needs to be expressed cell cycle starts.
  2. Less methylation of Proto onco DNA at promoter region.
  3. More acetylation of histone proteins around named Proto onco gene
    1. More expression of named proton once gene .
  4. More transcription of gene
  5. More mRNA formed.
  6. More translation of its mRNA.
  7. More name protein that starts cell cycle.
  8. Lead to uncontrolled cell division.
35
Q

Describe the result of mutations to promote a regions of tumour suppressed genes and proto-oncogenes

A
  1. Mutation in promoter regions for both tumour suppressor gene and proton onco genes
  2. Transcription factor cannot bind.
  3. So RNA polymerase is not stimulated.
  4. So no transcription of gene.
  5. So no mRNA formed.
  6. So no translation.
  7. Less protein.
  8. Can’t start or uncontrolled cell division.
36
Q

Describe the result of mutations to exons in tumour suppressed genes or proto-oncogenes

A
  1. Change in amino acid sequence.
  2. Change in structure due to different placement of hydrogen ionic and Dulfi bonds between all groups of amino acids.
  3. Protein cannot do its function.
  4. Faulty protein leads to increase or decrease in cell division.
37
Q

Gene

A

A base sequence of nucleotides that form a polypeptide chain

38
Q

A observed ratio is distinctly different to
expected phenotype ratios. The data
showed two phenotypes with a large
number of individuals and two
phenotypes with very low number of
individuals. . Explain this data

A

Genes are linked