6.1.1 cellular control Flashcards

(58 cards)

1
Q

acetylation/phosphorylation

A

the addition of acetyl/phosphate groups, to make them more negative so that the DNA can coil less tightly, and transcription can take place

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2
Q

methylation

A

the addition of methyl groups to make the histones more hydrophobic so that they can bind more tightly to eachother, preventing transcription

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3
Q

epigenetics

A

used to describe the control of gene expression by the modification of DNA

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4
Q

operon

A

group of genes that are under the same regulatory mechanism and are expressed at the same time

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5
Q

are operons prokaryotic or eukaryotic

A

prokaryotic

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6
Q

lac operon

A

group of 3 genes, lacZ, lacY and lacA, involved in the metabolism of lactose - structural genes

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7
Q

enzymes that the lac operon codes for

A

B galactosidase, lactose permease and transacetylase

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8
Q

regulatory gene of the lac operon

A

lacI, codes for the repressor protein which prevents the transcription of the structural genes in the absence of lactose

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9
Q

lac operon when lactose is absent

A

regulatory gene codes for the repressor protein
attaches to operator site
blocks the promoter site
this means RNA pol cannot attach
structural genes are not transcribed

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10
Q

when lactose is present

A

a little bit of lactose enters the cell by diffusion
attaches to the repressor protein
this changes the shape of the protein, so cannot attach to operator
RNA pol can attach to promoter
structural genes are transcribed
so enzymes are made

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11
Q

post transcriptional control

A

splicing

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12
Q

splicing process

A

pre- mRNA (introns and exons) is then changes when introns are removed and exons are joined, forming mature mRNA
a cap is added on 5’ end and a tail is added on 3’ end for stabilising

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13
Q

spliceosomes

A

the enzymes involved in splicing, can join the exons in a variety of ways, producing several versions of functional mRNA

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14
Q

factors that regulate when translation starts and stops

A
  • how long the mRNA lasts in the cytoplasm
  • inhibitory factors
  • initiation factors
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15
Q

post translational control

A

addition of non protein groups
folding into final shape
activation of proteins by cAMP

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16
Q

cAMP

A

cyclic AMP, can change the 3D shape of a protein, activating the active

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17
Q

activation of PKA

A
  1. PKA is an enzyme with 4 subunits
  2. when cAMP isnt bound the 4 units are bound together and inactive
  3. when cAMP binds, it causes a change in the enzymes 3d shape, releasing the active subunits, activating the enzymes
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18
Q

morphogenesis

A

the regulation of the pattern of anatomical development

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19
Q

homeobox genes

A

group of genes which all contain a homeobox

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20
Q

homeobox

A

section of DNA 180 base pairs long coding for a protein which is 60 amino acids long (a homeodomain)

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21
Q

homeodomain

A

60 amino acids long, and binds to DNA, and switches other genes on and off

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22
Q

hox genes

A

a group of homeobox genes that are only present in animals, responsible for the correct positioning of body parts

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23
Q

amount of hox genes in humans

A

39

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24
Q

how body plans are represented

A

cross sections through the organism showing the fundamental arrangement of tissue layers

25
somites
the segments in embryo that allow individual vertebrae to be developed, directed by hox genes
26
radial symmetry
seen in diploblastic animals like jellyfish, no left or right, just top and bottom
27
bilateral symmetry
seen in most animals means that organisms have both a left and right side and a head and a tail
28
asymmetry
seen in sponges which have no lines of symmetry
29
apoptosis
programmed cell death
30
how apoptosis shapes body parts
removes unwanted cells and tissues
31
what regulates mitosis and apoptosis?
hox genes
32
factors affecting the expression of regulatory genes
environment, internal and external stress and drugs etc
33
mutation
change in the sequence of bases in DNA or RNA
34
substitution mutation
mutation in which a single nucleotide changes the codon in which it occurs
35
degenerate code
multiple codons encode a single amino acid
36
nonsense mutation
a mutation that changes an amino acid codon to one of the 3 stop codons, resulting in a shorter and non functional protein
37
missense mutation
a base pair substitution that results in a codon that codes for a different amino acid
38
insertion mutation
a mutation in which one or more nucleotides are added to a gene
39
deletion mutation
a mutation in which one or more pairs are removed from a gene
40
frameshift
mutation that causes the reading frame of mRNA codons to shift (insertion or deletion)
41
no effect mutation
there is no effect on the phenotype of an organism because the normally functioning proteins are still synthesised
42
damaging effect mutation
phenotype of an organism is affected in a negative way because proteins are no longer synthesised, which can interfere with essential processes
43
beneficial effects of mutations
mutations often produce proteins with new or altered functions that can be useful to organism in changing environments
44
mutagens
physical and chemical agents that interact with DNA to cause mutations
45
physical mutagens
radiation x rays, UV light (break one or both DNA strands)
46
chemical mutagens
deaminating agents - chemically alter bases in DNA changing the base sequence
47
biological mutagens
viruses, base analogs, alkylating agents
48
chromosome mutation - deletion
due to breakage, a piece of chromsome is lost
49
chromsome mutation - inversion
a chromosome rearragement in which a segment of chromosome is reversed end to end
50
chromosome mutation - translocation
a section of one chromosome breaks off and joins another non-homologous chromosome
51
housekeeping genes
the genes that code for enzymes present in metabolic reactions that are always required
52
tissue specific genes
the genes that code for protein based hormones which are only required a certain times to carry out short lived responses
53
the different levels of gene regulation
transcriptional, post transcriptional, translational, post translational
54
heterochromatin
tightly wound DNA, where RNA pol cannot access the genes
55
euchromatin
loosely wound DNA where RNA polymerase can access the genes
56
suggest reasons why fruit flies are chosen for research into genes controlling development of body plan
- fewer public concerns over ethics of using flies - low cost - rapid reproduction rate - fruit fly genetics is understood well
57
why would mice be used in research of body plans? why not?
- low cost - similar to humans - however more ethical concerns
58