Cellular Control Flashcards

1
Q

Types of gene expression control

A

Transcriptional, post-transcriptional, translational and post-translational

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2
Q

Operon

A

Section of dna that contains a cluster of structural genes that are transcribed together, under a regulatory control system.

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3
Q

Reason for existence of lac operon

A

Allows E. coli to respire lactose when it is present but not produce the enzymes required when it isn’t

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4
Q

Sequence of lac operon

A

Regulator gene
Promoter gene
Operator gene
Structural genes (lac Z, lac Y and lac A)

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5
Q

Structural gene

A

One which actually codes for proteins that are then used

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6
Q

Specific genes in lac operon

A

B-galactosidase, lactose permease and transacetylase

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7
Q

Role of regulator gene

A

Codes for repressor protein which then binds to operator region or lactose

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8
Q

Lac operon when lactose is not present

A

Repressor gene codes for repressor protein which then binds to the operator region. RNA polymerase then can not access the promoter region so doesn’t bind and no structural genes are transcribed.

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9
Q

Lac operon in the presence of lactose

A

Repressor gene codes for the repressor protein. Lactose then binds to the repressor protein (essentially acting as a competitive inhibitor) changing its shape so it doesn’t bind to the operator region. RNA polymerase is then free to bind to the promoter region and transcribes the structural genes. These are translated into the enzymes which allow lactose to be used as a respiratory substrate.

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10
Q

Transcription factors

A

Proteins that bind to DNA to switch genes on or off by increasing or decreasing the rate of transcription.

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11
Q

Methylation

A

Addition of a CH3 group causing histones to become more hydrophobic and so bound tightly

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12
Q

Acetylation

A

Charge of histones change so they become less tightly bound

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13
Q

Histone modification

A

Methylation or acetylation changing the structure of the histones and so ability of the DNA to be transcribed

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14
Q

Heterochromatin

A

DNA is tightly bound around histones and cannot be physically accessed by RNA polymerase for transcription. Particularly during mitosis or meiosis where chromosomes become visible

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15
Q

Euchromatin

A

DNA is loosely wound around histones so the genes are available for transcription

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16
Q

RNA processing

A

Part of post-transcriptional control adding a modified nucleotide ‘cap’ to the 5’ end and a poly A tail to the 3’ end

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17
Q

RNA splicing

A

Removal of non coding introns to produce functional DNA

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18
Q

Examples of post translational control

A

Addition of non-protein groups
Modicficatoon of amino acids
Folding or shortening of the protein
Modification by c AMP

19
Q

Post translational activation by cAMP

A

Bind to proteins altering their 3D structure eg then changing the shape of their active site

20
Q

Example of modification by cAMP

A

Four units of protein kinase A bound together
cAMP binds changing the 3D structure so the subunits are released
PKA is activates

21
Q

Homeotic genes

A

Genes regulating where anatomical structures will develop

22
Q

Hox genes

A

Specific genes which control body plans in animals plants and fungi

23
Q

Homeobox sequence

A

A region of the Hox gene 180 based pairs long, so coding for a 60 amino acids protein called the homeodomaibn.

24
Q

Role of homeodomain protein

A

Binds to specific sites on DNA acting as a transcription factor for developmental genes

25
Q

Apoptosis

A

Programmed cell death

26
Q

Sequence of events in apoptosis

A

Signals trigger cell to die
Cells shrink as cytoskeleton breaks down
DNA, proteins and organelles are degraded by enzymes
Blebs containing digested contents form on the cell surface membrane
Blebs are engulfed by phagocytes

27
Q

Use of apoptosis in development

A

Some cells triggered to die in order to create accuracy eg trimming and shaping hands and feet

28
Q

Stimuli for apoptosis

A

Internal such as DNA damage detected

External such as stress caused by lack of nutrients so that cells can not undergo mitosis

29
Q

Mutation

A

Permanent change in the sequence of nucleotide bases that can be induced or spontaneous

30
Q

Types of mutation

A

Substitution
Deletion
Insertion

31
Q

Point mutation

A

Insertion, substitution or deletion of a single nucleotide

32
Q

Silent mutation

A

Mutation occurring in non coding region

33
Q

Nonsense mutation

A

Change of amino acid to a STOP codon meaning protein is cut short

34
Q

Missense mutation

A

Change in order of nucleotides which causes a change in amino acid sequence

35
Q

Frame shift

A

Insertion and deletion of nucleotide causes a movement in the reading frame as codons are no longer read in sequence

36
Q

3 types of mutagen

A

Physical, biological and chemical

37
Q

Physical mutagens

A

Ionising radiation

38
Q

Biological mutagens

A

Viruses

39
Q

Chemical mutagens

A

Base analoguse
Deaminating agents
Alkylating agents

40
Q

Chromosome mutation

A

Mutation affecting the whole chromosome

41
Q

4 types of chromosome mutation

A

Deletion
Duplication
Translocation
Inversion

42
Q

Beneficial mutation

A

One which confers evolutionary advantage on carrier eg antibiotic resistance in bacteria

43
Q

Neutral mutation

A

Neither advantageous or disadvantageous

44
Q

Harmful mutation

A

Characteristic produced causes disadvantage to the organism eg genetic disease