RNA synthesis Flashcards

1
Q

Main function of transcription and does the language remain the same?

A

mRNA synthesised in the nucleus and same language of nucleic acids

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2
Q

Main function of translation and does the language remain the same

A

Protein production from mRNA

Different language form nucleic acid to protein

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3
Q

How many nucleotides are there in the human genome?

A

3.2 x10^9

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4
Q

How many homologs do chromosomes have and what are they referred to as?

A

2 and they’re known as paternal and maternal homologs

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5
Q

What is the key function of chromosomes?

A

To carry genes

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6
Q

What are centromeres made up of and what is there key function?

A

• Centromere is made up of DNA and key function is to keep the chromosome attached to the spindle fibre during mitosis.

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7
Q

Where are telomeres located and what is there main function?

A

○ Located at the end of the chromosome
○ Double strand
○ Six base pair repeat

Protects end of chromosome by preventing fusion from neighbouring chromosomes

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8
Q

How many autosomes and sex chromosomes are there?

A

22 autosomes

1 sex chromosome

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9
Q

What is the intergenic region and what does it contain?

A

The region of DNA between genes which have no current function

    Contains pseudo genes
Repetitive DNA
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10
Q

What is a gene and its properties such as size and its affect on phenotype?

A
  • Unit of heredity, contains instructions for an organisms phenotype
  • DNA segment containing instructions for making a particular product
  • Differ in size
  • Differ in number of introns and exons
  • Cluster into families
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11
Q

What is the promoter?

A

a region involved in ensuring RNA polymerase combining for transcription.

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12
Q

What does RNA make and what does it catalyze?

A
  • DNA transcribed into RNA

* Catalyses the formation of phosphodiester bonds

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13
Q

Types of RNA polymerase

A
  • RNA polymerase 1- Most ribosomal RNA
  • RNA polymerase 2- Protein coding, microRNA
  • RNA polymerase 3- tRNA, 5S rRNA
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14
Q

During RNA synthesis, how many bases are transcribed roughly?

A

• About 1.25-1.75 kb per min so quite fast

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15
Q

During RNA synthesis, how do polymerases work and the effect on the number of transcripts from a gene simultaneously?

A
  • Many polymerases work on the same gene

* Many transcripts from a gene simultaneously

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16
Q

Why are Transcription factors required?

A

• Required to initiate or regulate transcription

17
Q

What does the promoter contain to which RNA polymerase 2 binds to and how many bp is it?

A

Containts TATA box which is 30 bp.

18
Q

Transcription(Initiation)

A

• Eukaryotic promoter regions contain a DNA sequence called the TATA box
• Transcription factor (TFIID ) sub unit, the TBP, recognises the TATA box and binds.
• The binding of TFIID enabled the adjacent binding of TFIIB and TFIIA.
○ TFIIB is responsible for linking RNA polymerase to the complex
○ TFIIA stabilises the complex
• TFIIF is already associated with the RNA polymerase when RNA polymerase binds to the TFIIA-TFIIB-TFIID complex.
• TFIIE and TFIIH both associate with RNA polymerase and initiation is complete.
○ TFIIH breaks apart the double helix at the transcription starting point
○ TFIIH also phosphorylates RNA polymerase II, so it can start transcription.

19
Q

Transcription(Elongation)

A

RNA strand gets longer by the addition of nucleotides at the growing 3’ end.

20
Q

Transcription(Termination)

A

• When a sequence of DNA, known as a terminator and located after the stop codon, is reached transcription ends

21
Q

What are untranslated regions and what are they required for?

A

• Are transcribed but not translated as they’re required for regulation

22
Q

what is the 5 Primer UTR responsible for?

A

involved in the regulation of translation

23
Q

What is the 3 primer UTR responsible for?

A

regulation of mRNA stability and miRNA binding

24
Q

RNA processing(Capping)

A

• Capping:
○ 5’ end becomes modified after 25 nucleotides of RNA have been synthesised.
§ A guanine is added to the 5’ end and an enzyme called methyl transferase, methylates guanine to give rise to 7 methylguanine cap.
□ This cap protect the degradation of mRNA

25
Q

RNA processing(Polyadenylation)

A

• Polyadenylation:
○ mRNA is trimmed by an enzyme at the 3’ end
○ The transcript is finished off by a second enzyme that adds repeated Adenine bases to the cut end
○ Poly-A tail is formed making the transcript more stable and protects pre-mRNA from RNAses which digests RNA in the cytoplasm as it moves out the nucleus.
○ The longer the poly-A tail the more stable the RNA is

26
Q

What is capping and polyadenylation required for?

A

Required for stability

27
Q

What is RNA splicing

A

Removal of introns and joining of exons

28
Q

Splicing

A

• Special sequences in a pre-mRNA signal the beginning and the end of an intron
○ Recognised by snRNPs
• At GU we have the 5 primer splicing region
• At AG we have the 3 primer splicing region
• The lariate structure loops to join the branch point as is disposed off leaving the exon which joins the second exon.

29
Q

What is alternative splicing?

A

There are splice variables meaning during translation different proteins are synthesised