Lecture 2/3 Flashcards

1
Q

approximately how many genes are we estimated to have?

A

40,000 (many noncoding ones)

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2
Q

how are chromosomes numbered?

A

by size (1 is biggest)

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3
Q

what are the 3 major differences between RNA and DNA?

A
  1. ribose vs. deoxyribose sugar
  2. Uracil instead of Thymine
  3. most RNAs are single stranded
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4
Q

What is on carbon 2 in RNA? DNA?

A

RNA: hydroxyl
DNA: hydrogen

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5
Q

RNA is single stranded, how does it get interesting secondary/tertiary structures?

A

by binding to itself – it needs to fold into certain structures to function / so certain amino acids can attach

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6
Q

How does a molecule carry information?

A

base sequence

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7
Q

how is information from a gene transmitted to future generations?

A

DNA replication

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8
Q

what 2 mechanisms allow genetic information to change?

A
  1. recombination
  2. mutations
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9
Q

how does DNA-encoded information govern the expression of phenotype?

A

gene functions – DNA instructions are transcribed into RNA and then translated into proteins, which influence an organism’s phenotypes

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10
Q

how do somatic cells spend their time?

A

either in G0 (hanging out) or actively going through mitosis (cell cycle)

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11
Q

are germ cells always haploid?

A

no, they’re initially diploid during embryogenesis before they’re differentiated

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12
Q

what cell cycle do gametes go through?

A

meiosis

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13
Q

what is the genome

A

the sum of genetic information in a haploid set of chromosomes

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14
Q

what is a haploid genome

A

the genetic content of a gamete

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15
Q

how is the DNA content of a haploid cell represented?

A

n

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16
Q

how is the DNA content of a diploid / somatic cell represented?

A

2n

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17
Q

how is the DNA content of a tetraploid cell represented?

A

4n

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18
Q

how many chromosomes in a human egg?

A

23

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19
Q

how many chromosomes in a human somatic cell?

A

46

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20
Q

does the number of chromosomes in an organism relate to the complexity of the organism?

A

no

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21
Q

how long is a full cell cycle for a human cell in vitro?

A

approx 24 hours

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22
Q

What happens at G1 in the cell cycle?

A

it is the checkpoint for mitosis, proteins for DNA replication are made; takes approx 10 hrs

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23
Q

What happens at S in the cell cycle?

A

DNA replication, ~9hrs in vitro

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24
Q

What happens in G2?

A

checkpoint for DNA replication, proteins for mitosis are made; ~4hrs

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25
Q

what happens in mitosis, and what are the 4 stages?

A

cell division: ~1hr
Prophase
Metaphase
Anaphase
Telophase

26
Q

what cells are postmitotic at birth?

A

nerve cells

27
Q

if there are mistakes in DNA replication, at what point in the cell cycle would they be fixed?

28
Q

In mitosis, how many chromosomes do daughter cells have in comparison to the parent cells?

A

the same number

29
Q

once divided, is every part of the daughter cells of a fertilized egg exactly the same?

A

only if they’re twins, otherwise at least the cytoplasmic components are likely to be different

30
Q

How is DNA compacted?

A

DNA is wrapped around histone protein cores to make a nucleosome

31
Q

what repeating unit is formed by nucleosomes?

32
Q

In a non-dividing somatic cell, what is the DNA content of the cell?

33
Q

How is DNA organized during interphase?

A

Before cell division, DNA exists in a loosely organized form called chromatin, which is not visible as chromosomes.

34
Q

How is DNA organized during prophase?

A

As the cell enters prophase, the chromatin coils and condenses, becoming tightly packed into visible chromosomes.

35
Q

Is DNA condensed during mitosis?

A

yes, and it is visible as chromosomes

36
Q

what is it called when DNA is wrapped around histones to fit in the nucleus?

A

compaction

37
Q

are chromosomes randomly placed or organized

A

organized, they each have their own little territory

38
Q

what are the three possible models of DNA replication?

A

semi-conservative (correct)
conservative
dispersive

39
Q

what is semi-conservative DNA replication

A

2 parental strands separate and each form template strands; new strand forms by insertion of complementary base pairs, single double helix becomes 2 identical daughter double helices

40
Q

what is the concept of conservative DNA replication

A

parental double helix remains intact, both strands of daughter helices are newly synthesized

41
Q

what is the concept of dispersive DNA replication

A

both strands of both daughter helices contain original and newly synthesized DNA

42
Q

In the experiment testing what the correct model of DNA replication is, how did they grow E.coli?

A

First in media containing 15N (heavy isotope) and then 14N (normal isotope)

43
Q

Once the 15N bacteria grow for one generation in 14N and are centrifuged, where are the DNA bands?

A

there was one band between where one would expect 15N and where you’d expect 14N

44
Q

Once the 15N bacteria grow for two generations in 14N and are centrifuged, where are the DNA bands?

A

you get the intermediate band and also the 14N band because of semi-conservative replication

45
Q

what kind of bonds does DNA polymerase catalyze?

A

phosphodiester

46
Q

what are the two stages involved in DNA replication?

A

initiation and elongation

47
Q

what happens in DNA initiation?

A

proteins open up the double helix and prepare it for complementary base pairing

48
Q

what happens in DNA elongation?

A

proteins connect the correct sequence of nucleotides on newly formed DNA strands

49
Q

What are the proteins that bind to the origin site, unwind the helix, and keep the replication bubble open?

A

initiator protein, helicase and single-stranded binding proteins

50
Q

how many chromosomes do bacteria have?

51
Q

what does primase do and where does it work?

A

primase synthesizes RNA primer, which can only be added onto the 3’ end

52
Q

in which direction does DNA pol iii elongate?

A

5’ to 3’

53
Q

what is the difference between the leading and lagging strands?

A

leading strand has continuous synthesis, whereas the lagging strand has discontinuous synthesis

54
Q

what is an okazaki fragment?

A

short DNA fragments on the lagging strand (because nothing is added on the 5’ end during replication)

55
Q

what 2 processes must occur after primer elongation?

A

primer must be replaced with DNA sequence and okazaki fragments must be covalently joined by DNA ligase

56
Q

what is used to degrade RNA primer and in which direction does it work?

A

DNA pol i degrades the primer using 5’ to 3’ exonuclease activity and fills in the missing nucleotides

57
Q

what is used to covalently join okazaki fragments?

A

DNA ligase

58
Q

where does DNA pol i work?

A

at the free 5’ end

59
Q

what is used to proofread, and what direction does it go?

A

DNA pol iii, and it has exonuclease activity in the 3’ to 5’ direction

60
Q

what is chewback in DNA replication?

A

the 3’ to 5’ proofreading activity – for 1 error it might remove 1000bps and then fill it in again

61
Q

what forms when ligase links 2 DNA fragments together

A

ligase catalyzes the formation of phosphodiester bonds with the energy from bond formation

62
Q

when helicase unwinds DNA, what happens ahead of the replication fork?

A

it creates supercoiled DNA