1.14. Organization of genetic information Flashcards

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1
Q

both pro- and eukaryotes use DNA as…
(the only exception…)

A

genetic material, but there are differences in their DNA organization
retroviruses (using RNA)

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2
Q

location and number of DNA molecules (p vs e)

A

prokaryotes:
- in the nucleoid, 1 circular DNA (no. of DNA mol. equal to the number of chromosomes)
eukaryotes:
- in the nucleoplasm/nucleus, 2 or more linear DNA (always even number)

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3
Q

types of DNA sequences (p vs e)

A

prokaryotes:
- the majority of the DNA codes for proteins except for regulatory sequences (promotors, terminators…) + codes for rRNA/tRNA
- coding sequences not interrupted by non-coding
eukaryotes:
- coding regions make up only a smart portion of the genome, the rest is non-coding (in humans taking up 97% ), coding regions are composed of introns and exons

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4
Q

association with proteins (p vs e)

A

prokaryotes:
- “naked” - not joined with proteins
eukaryotes:
- associated with globular proteins called histones which control the gene expression

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5
Q

mitosis (natural process of cloning) preserves

A

the genom

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6
Q

histones

A
  • globular proteins associated with the DNA in eukaryotes
  • the DNA coils around them and condenses/supercoils, forming chromosomes (they provide the structure to the chromosome)
  • soluble in water
  • contribute to gene expression
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7
Q

types of non-coding sequences

A

1|regulatory sequence
2|introns
3|short tandem repeat sequences (STR seq.)
4|codes for tRNA and rRNA
- they can code for anything but proteins (only coding parts of DNA code for proteins)

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8
Q

STR seq. and regulatory sequences are in the ____ of the DNA (__), and introns are in the ___ of the DNA but…

A

non-coding part, not a part of a gene, coding part, they get spliced out (not in the mature mRNA) - they don’t code for anything

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9
Q

short tandem repeat sequences

A
  • not a part of the gene (non-coding DNA)
  • composed of repeating units (5-300 bp long) that repeat as many as 100 000x along the DNA)
  • unique for every single person (size and sequence differ) - STR analysis the basis for DNA fingerprinting
  • can afford to mutate - doesn’t code for anything - while e.g. insulin gene has to be the same in all people for it to perform its function (it would decrease the “quality” of the organism - evolutionary speaking)
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10
Q

regulatory sequences

A

promotors and terminators - on the DNA but don’t get transcribed (non-coding, have a regulatory function)

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11
Q

Where are STR seq. mainly found

A

in centromeric and telomeric regions of the chromosome

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12
Q

what happens to the DNA length in DNA replication

A

terminal (end) segments of the DNA (3’ to which RNA primers attached) are lost as no DNA nucleotides can attach to the 5’
- this is why no coding parts of the DNA on the ends

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13
Q

telomerases

A

STR sequences on the DNA ends - they have a protective function for the DNA - get lost during DNA replication and once they are used up that DNA can never replicate again (otherwise would lose genes) - cell dies

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14
Q

genes for tRNA and rRNA

A

stretches of DNA that are transcribed into mRNA but aren’t translated (4th non-coding type of sequence)

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15
Q

alternative splicing

A

one gene can encode for more than one protein

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16
Q

telomerase

A

recovering telomers (cancer cells have a lot of it so they are capable of counless divisons)

17
Q

nucleosome =

A

8 histones + 2 turns of the DNA around them

18
Q

What prevents the DNA strand from entangling and breaking (leading to mutation)?

A

formation of nucleosomes, that is, the beads on a string structure

19
Q

how do histones regulate gene expression

A

genes in condensed/supercoiled DNA (coiled around histones) are not approachable to transcription enzymes (RNA polymerase) therefore no gene expression

20
Q

histone N-terminal tails

A

link together and pull nucleosomes together which provide further stabilization of the condensation - protruding from each histon

21
Q

linker DNA

A

short DNA section that links 2 nucleosomes

22
Q

H1 histone

A

binds the DNA to the core of nucleosome, stabilizing its condensation

23
Q

draw a complex of 2 nucleosomes

A

24
Q

acetyl group (with and without)
- acetic acids (CH3-COO^-)

A
  • abundant in the nucleus
  • with AC - histone tails don’t join together, don’t pull histones closer so level of DNA condensation decreased, increasing gene expression
  • without AC (normal) - histones pulled together, higher level of DNA condensation, reduction in gene expression
  • it impacts the conformation of histone tails and therefore impacts the expression of genes
25
Q

modification of histone tails by acetyl groups

A

acetylation