molecular genetics Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

what are the differences between RNA and DNA

A

RNA (ribonucleic acid)
- single stranded
- uracil instead of thymine
DNA (deoxyribonucleic acid)
- double stranded
- thymine instead of uracil

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what are the nitrogenous bases? which are pyrimidines and purines?

A

pyrimidines (single ring)
- thymine (DNA) [uracil in RNA]
- cytosine
purines (double ring)
- adenine
- guanine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what makes up a nucleotide?

A

Pi - sugar [ribose; 5C sugar, deoxyribose; ribose minus one oxegyn] - nitrogenous base [AUCG, ATCG]

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

how does DNA condense in eukaryotes?

A
  • DNA gets wrapped around histones (protein)
  • Organize histone packets into a nucleosome
  • nucleosomes are looped
    2 of those make a metaphase chromosome
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

how does DNA condense in prokaryotes?

A

super coiling

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

topoisomerase

A

relieves tension/prevents DNA from breaking (also known as gyrase)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

helicase

A

cuts H-bonds (unzips DNA)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

SSBP

A

(single strand binding proteins)
keep H-bonds from re arranging

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

DNA polymerase III

A

synthesizes new DNA strands
BUT
- cannot start on its own
- can only add new nucleotides to free 3 end
- only synthesized in 5 to 3 end direction (new strand goes 5 to 3)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

primase

A

lays down RNA primer 5 to 3 for DNA polymeraise to start

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are telomeres? and what do they do?

A

protects eukaryotic genes from losing important DNA when primers are removed

telomerase: can restore telomeres BUT as you age telomerase is less active

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

DNA polymerase I and II

A

excises primers and replace with nuceotides + proofread and excise typos

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

ligase

A

makes phosopdiester bonds between DNA fragments (okazaki fragements)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what it the difference in the synthesis of the leading and lagging strands

A

the leading strand is synthesized continuously whereas the lagging strand is synthesized in okazaki fragments since DNA poly can only work off a free

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is more harmful a base pair substitution and a frameshift mutation? and why?

A

frameshift mutation because an addition or deletion of a base affect all the codons after

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what are the three kinds of base pair substitutions?

A

base pair substitution: A instead of C (for example)
- nonsense: STOP codon
- missense: differents AA
- silent: no change (redundant codon)

12
Q

what is a gene

A

section of DNA that codes for a protein

13
Q

central dogma of biology???

A

gene – trancribed to — mRNA — translated to —protein (sequence of AA)

14
Q

what enzyme is responsible for transcription?

A

RNA polymerase: reads the template strand from 3 - 5 so that mRNA runs 5 - 3

15
Q

what direction do the coding and template strands run

A

template (anti sense): 3 - 5
coding (sense): 5 - 3

16
Q

what does tRNA do

A

tRNA brings AA to the ribosome, it has anticodons specific to the AAs needed

17
Q

in eukaryotes what needs to happen to the mRNA before entering the cytoplasm

A

mRNA modification:
- cap and tailing: GGGG cap and poly A tail
- splicing: SnRNPs exise the introns (non coding region)
- alternative splicing: introns are not always introns, regulated with regulatory proteins

18
Q

why do eukaryotes need to do mRNA modification

A

because the mRNA starts to degrade in the cytoplasm and must be protected from that with the caps
splicing so that the ribosome creates the right protein

19
Q

explain translation

A
  1. mRNA settles into P (peptide) site of the ribosome
  2. tRNA brings AA to A site (acceptor)
  3. ribosome makes peptide bond
  4. ribosome shifts (3 codons over)
  5. process repeats until stop codon)

exit site of the ribosome: tRNA id removed/leaves to get other AAs

20
Q

what are the components of an operon?

A

CAP, promoter (ex. TATA box), operator, structural genes

21
Q

explain an example of the off model

A

lactase: LacI inhibitor blocks RNA polymerase from transcribing by binding. lactose binds to the inhibitor to remove it once there is lots of lactose to be digested

22
Q

tryptophan is an explain of what model of regulation?

A

on model: always on unless you dont need it
tryp activates the inhibitor when there is lots of tryp already in your system (when u have another source, ex chicken)

23
Q

gene regulation in eukaryotes?

A

much messier, not neatly organized

transcription factors: regulator proteins that binds to a part of DNA to regulate transcription
- activators
- inhibitors

24
Q

difference in DNA/DNA replication in pro and eukaryotes?

A

prokaryotes:
- small, circular
- no junk DNA (no mRNA modification)
- supercoiling
- single origin of replication
- don’t lose length cuz of primers cause circular (no telomeres)
- translation starts when transcription is occuring

eukaryotes:
- large, linear
- lots of “junk” DNA (repetitive sequences, genome stability, and evolution, introns) [mRNA modification]
- DNA coils around histones
- many origins of replication
lose a few nucleotides at endsm [telomeres]
- translation and transcription happen at some time (mRNA must be transported)

24
Q

explain DNA replication

A
25
Q

the genetic code is… (explain)

A

universal and redundant

26
Q

Explain how you could use genetic technology to insert a gene into a different organism?

A
27
Q

What is a plasmid

A

A same circular section of dna inside bacteria, commonly used for cloning bacteria, separated from bacterial DNA

We can insert genes into a plasmid using restriction endonuclease