Genomics Flashcards

1
Q

Describe the role of telomerase in cancer cells [3]

A
  1. Extends telomeres to 3’ -OH ends of template DNA
  2. Telomeres are non-coding DNA
    » protect essential genes from being eroded as DNA shortens due to ERP
  3. Allows cells to divide indefinitely (immortal / no apoptosis)
    * REJECT: uncontrolled CD (stem cell CD is well-regulated)
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2
Q

Suggest 2 ways telomerase can be inhibited as a form of cancer therapy [2]

A
  1. asRNA - bind to mRNA template coding for telomerase
  2. Competitive inhibitors - block AS of TERT
    » prevent catalysis of formation of PPD bonds
    » prevent elongation of telomeres
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3
Q

Describe 2 ways of PTM [2]

A
  1. Activation by biochemical modification
    » glycosylation/phosphorylation/proteolytic cleavage
  2. Tag with UBIQUITIN&raquo_space; enter PROTEOSOMES
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4
Q

Explain how mature RBCs can regulate the Tsl of the stored mRNAs to prevent wastage of resources [2]

A
  1. TRANSLATIONAL REPRESSOR PROTEIN binds to 5’ UTR

2. Prevents small RS from binding&raquo_space; formation of Tsl IC

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5
Q

Discuss if protein glycosylation is influenced by genes expression [2]

A

NO - genes do not code for oligo

YES - enzymes that mediate glycosylation are coded for by genes

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6
Q

Explain how the structure of the centromere allows it to carry out its functions [3]

A

COMPULSORY POINT 1
» non-coding tandem repeats&raquo_space; specific 3D conformation

  1. Allow sister chromatids to bind to each other via kinetochores
  2. Allow spindle fibres to bind
    » allow for alignment of chromosomes at the equator during metaphase
    » subsequent separation of sister chromatids to opposite poles
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7
Q

State 2 advantages of alternative splicing [2]

A
  1. Increase coding capacity / protein diversity

2. More rapid response to changing environmental conditions / cellular demand

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8
Q

Explain the role of rRNA [2]

A
  1. Small RS - bind to mRNA via CBP (A2T, C3G)
  2. Large RS
    » bind to aa-tRNAs at P and A site
    » forms peptidyl transferase to catalyse the formation of peptide bonds b/w adjacent AAs
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9
Q

Explain how the structure of RNA pol enables it to perform its function [4]

A
  1. AS has a specific 3D conformation that is complementary in shape and charge to DNA template and the incoming nucleotides
    » catalyse the formation of PPD bonds
  2. DNA-binding domain has a specific 3D conformation that is complementary to the promoter&raquo_space; initiate Tsc
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10
Q

Compare the synthesis of the leading and lagging strand [4]

A
  1. Type of synthesis
    » continuous vs. discontinuous
  2. Direction of synthesis
    » towards vs. away from RF
  3. Number of primers
  4. DNA ligase to seal the nick by catalysing the formation of PPD bonds
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11
Q

Suggest why DNA replication is “asymmetrical” [2]

A
  1. DNA POL works in 5’ to 3’, adding dNTPs to 3’ -OH

2. Template strands are antiparallel

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12
Q

Explain how Fig 1.1 shows SCR [3]

A
  1. Parental DNA molecule separates into 2 single strands which serve as TEMPLATES
    »> via CBP, A2T C3G
  2. 2 daughter molecules each consisting 1 original + 1 newly synthesised
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13
Q

Explain the importance of H-bonding in DNA structure [2]

A
  1. Hold strands together to form a DNA molecule
  2. Numerous H-bonds&raquo_space; confer stability
  3. CBP - A2T, C3G
  4. Weak bonds&raquo_space; easily broken for strand separation for SCR/Tsc
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