gen bio 2 exam 3 Flashcards

1
Q

How many proteins can a cell have?

A

5000

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2
Q

DNA ->?->RNA->?->protein

A

Transcription
Translation

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3
Q

Nucleotide

A

Phosphate, Sugar, Nitrogenous base

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4
Q

What are the nitrogenous bases?

A

Purines: Adenine, guanine
Pyrimidines: Cytosine, Thymine, Uracil

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5
Q

Nulceoside

A

Pentose sugar + nitrogenous page

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6
Q

Difference between ribose and deoxyribose

A

Ribose has an extra o at c’2

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7
Q

Attatchments of Nucleotide

A

Phosphates attach to c5’, bases attach to c1’, and second nitrogenous bases in chain attached to c3’
Complimentary strands of 5’->3’

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8
Q

Semiconservative Replication

A

When DNA is duplicated, the resulting daughter strands are 1/2 nascent, and 1/2 parent

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9
Q

Lagging Strand

A

The bottom strand in duplication runs 5’->3’, but duplication needs to go 5’->3’ so RNA primease makes primers where RNA polymerase then runs 5’->3’

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10
Q

Okazaki Fragment

A

Fragments of lagging strand, DNNA polymerase removes the primers and ligase connects the fragments

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11
Q

DNA Polymerase

A

Reads the parent strand and synthesis the daughter DNA, at 50 bases/second, 1/100,000 bases are mutated.

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12
Q

Ways to fix errors in DNA replication

A
  • DNA polymerase can correct its own mistakes
  • Mismatch repair is where a second DNA polymerase proofreads, and when it comes across and error it cuts out a section around the error, and ligase puts new section in
  • Excision Repair: extra nucleotide inserted, and Polymerase cuts it out and a ligase repairs
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13
Q

Telomeres

A

Repeated TTAGGG 200-2500 times to form a cap at the end of DNA, as due to DNA polymerase running 5’->3’ and a primer is needed, a few nucleotides are lost at the caps
Many cancer cells have active telomerase which repairs the telomere caps

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14
Q

3 main types of RNA

A

mRNA - messenger RNA
tRNA - Transfer RNA
rRNA - Ribosomal RNA

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15
Q

Transcription, 3 main steps and what is needed (transcription)

A

What is needed:
1) precursors (ATp,GTP,CTP,UTP)
2) energy (ATP)
3) enzymes (RNA polymerase)
4) Template (DNA)
3 main steps:
1)Initiation
2)Elongation
3)Termination

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16
Q

Initiation (transcription)

A

Promoter (section of DNA where the polymerase attaches to)

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17
Q

Elongation (transcription)

A

DNA is unwinded in the bubble, RNA polymerase adds RNA nucleotides to the template strand )5’->3’)

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18
Q

Termination (transcription)

A

Termination sequence is section of DNA that makes the RNA polymerase detatch, then DNA winds back

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19
Q

5’ cap

A

a 5’ cap is added to pre-mRNA, added to the 5’ end and is 7-mehtylguanine.

Helps stabilize mRNA
Assists w/ ribosome loading

20
Q

poly A tail

A

added to the 3’ end, hundreds of adenines

helps stabalize mRNA
helps w/ nuclear export

21
Q

Splicing

A

occurs to mRNA, introns are removed by snRNPs that form a spliceosome

22
Q

Translation

A

INITIATION
tRNA attatched to the small subunit, and then the large ribosomal subunit attatches.

ELONGATION
The anti-codon matches w/ codon, and when the amino acid is attatched the ribosome move forward 1 codon on the mRNA, and the tRNA moves to the exit site and a new tRNA enters the A site before movement. This repeats ntil termination sequence

TERMINATIOn

when termination codon is met (UUA, UGA, UAG) a termination factor attatches to the P site, and complex dissasembles

23
Q

Start and end codons

A

Start ; AUG
End: UUA, UAG, UGA

24
Q

Polyribosomes

A

Have a bunch of ribosomes translating one mRNA at once

25
Signal Sequence
A sequence of amino acids that tells the Ribosome to bring the mRNA from the cytosol to finish translation in the Rough Endoplasmic Reticulum The Protein made is partially in rER, and is fully release din lumen of rER, sent to Golgi thru transport vesicle
26
Golgi
Cis and trans face, adds sugars to proteins, and sends them away from the trans face
27
Secretory vesicle
A transport vesicle but waits until a signal to merge w/ plasma membrane
28
Chaperones
Proteins that help amino acids properly fold
29
Proteolysis
When a newly formed AA chains is cut to form a properly folded protein
30
Glycosylation
Golgi does this, adding sugar chains to proteins for targeting/recognition
31
Phosphorylation
"on" and "off" for proteins, adding of negative phosphate group.
32
Kinase
Adds the phosphates in phosphorylation
33
Phosphatase
Remove phosphates from proteins
34
Inducible vs Repressible genes
Inducibles start off and are induced by high "substrates", and repressed by low levels of substrate, heat chock proteins repressibles start on, and are repressed by high levels of product, glycolysis when high ATP glycolysis stops
35
mRNA degredation
mRNA not stable in the cytosol mRNA turnover, how much mRNA is made vs how fast it is broken down
36
Proteosome
Protein machinery that breaks down proteins to their amino acid constituents, only breaks down things marked with ubiquitin
37
The cause of some neurodegenerative disorders
The proteosome doesn't function properly leading to accumulation of proteins
38
Epistasis
Expression of one gene affects another
39
Expressivity
The degree to which a genotype is expressed in an individual
40
Polydactylism
Having extra digits
41
42
Helicase
Unwinds and opens DNA
43
RNA primase
forms the RNA primer on the DNA template for polymerases to attach to
44
DNA polymerase
attaches to 3' of previous nucleotide, and builds DNA strand
45