Introduction to the Control of Gene Expression Flashcards

1
Q

how many genes does the genome contain and how many are expressed?

A

-contains 50,000 genes but only 10,000 expressed

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2
Q

what is differential gene expression?

A

the different interpretation of the genome in each cell

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3
Q

explain how gene expression is regulated in terms of time and space

A
  • time: embryos express different genes to adults

- space: different tissues or cells express different genes (eg brain vs heart)

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4
Q

where are totipotent cells found and what is their differential ability?

A
  • found in early embryos

- have the ability to differentiation into any type of cell

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5
Q

what type of cells can pluripotent cells differentiate into?

A

most cell types but not placental tissue

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6
Q

what do certain transcription factors do when added to specialised cells?

A

-de-programme them and make them pluripotent

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7
Q

what is β thalassaemia caused by?

A

by the insufficient expression of β-globin

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8
Q

why don’t zygotes need to transcribe genes?

A

they have maternal pre-formed mRNA

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9
Q

explain how the ribosome finds the start sequence?

A

it binds to and recognizes the cap and will keep going until it recognizes the start sequence which is the first AUG near the kozak sequence.

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10
Q

what two proteins recognize the cap?

A

EFI3 and EFI4

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11
Q

how does ferritin work?

A
  • a protein that acts as a sponge for ions
  • binds Fe2+ and retains in cytoplasm as store for excess
  • when [Fe2+] , Fe binds to Fe starvation inhibitor and translation occurs as the ribosomal subunit access to the mRNA
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12
Q

what is the function of the UTRs?

A

they stabilise the mRNA and regulate the life span

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13
Q

what does the 3’ UTR sequence do?

A

causes proteins to bind which protects the RNA from degradation

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14
Q

what is the promoter region in eukaryotes and prokaryotes

A

TATA box and pribnow box

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15
Q

What is β-thalassaemia and what kind of mutations cause this disease?

A
  • blood disorder that reduces the production of haemoglobin.
  • the β-globin protein is structurally normal (unlike sickle cell disease).
  • Mutations that cause this disease are usually single base changes
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16
Q

Give examples of post translational control

A

EARLY EMBRYOGENESIS:

  • During the first 4-8 weeks of cell division, there is no gene expression.
  • At the end of blastocyst formation, genes are expressed due to the up-regulation of translation from maternally-derived preformed mRNAs.

ENVIRONMENTAL STRESS:
-exposure to heat shock or pathogens can cause global changes in translation.
There are many specific examples, such as ferritin.

17
Q

what is the function of the 5’ UTR?

A

determining how efficiently the ribosome initiates translation.

18
Q

what are miRNAs, and what is their function and how many are encoded in the human genome?

A
  • 500 small non-coding RNAs that are transcribed by RNA Pol II
  • they act to control post-transcriptional regulation of up to 1/2 of human genome
19
Q

describe the synthesis of miRNAs and explain how they work

A
  • each precursor miRNA transcript is processed to form a double-stranded intermediate
  • further processed to form a mature, single-stranded miRNA.
  • this miRNA assembles with a set of proteins into a complex called RISC, which then searches for mRNAs that have a nucleotide sequence complementary to its bound miRNA.
  • depending on how extensive the region of complementarity is, the target mRNA is either rapidly degraded by a nuclease within the RISC (this happens when there is an extensive match)
  • or transferred to an area of the cytoplasm where other cellular nucleases destroy it (this happens when there is a less extensive match).