6. DNA Flashcards

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1
Q

Nucleosides vs nucleotides

A

pentose (5 carbon sugar) + nitrogenous base at C1 vs phosphate at C5 + pentose (5 carbon sugar) + nitrogenous base at C1

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2
Q

Ribose vs deoxyribose

A

Has -OH at C2 vs has -H at C2

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3
Q

Know Chargaff’s rule

A

A + G = C + T. Purines = Pyrimidines (ie. A%=T%, C%=G%)

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4
Q

Purines vs pyrimidines. Are purines ever seen on opposite sides of DNA strands?

A

A,G; cyclohexane + cyclopentane ring vs C, U ,T; cyclohexane ring. BOTH ARE AROMATIC —> very stable and unreactive which is important when storing and analyzing them. Purines are NEVER seen on opposite sides of DNA strands b/c they never pair together (ie. purines bond w/ pyrimidines)

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5
Q

What does Watson-Crick model tell you?

A

double helix with antiparallel strands, bases facing inside and phosphate groups facing outside

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6
Q

B DNA vs Z DNA. Major groove vs minor groove

A

Right handed helix vs left handed helix (has zigzag appearance). Big gap vs little gap

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7
Q

Histones vs nucleosome vs chromatin

A

The protein around which DNA winds itself VIA ELECTROSTATIC INTERACTIONS vs a bunch of histones + wound DNA together vs a bunch of nucleosomes

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8
Q

Heterochromatin vs euchromatin. Constitutive vs facultative heterochromatin

A

compacted chromatin during interphase, dark light microscopy, genetically inactive vs dispersed chromatin during interphase, light microscopy, genetically active. Repetitive DNA for structural roles (ex: centromeres and telomeres) vs coding regions of DNA that are silenced

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9
Q

Topoisomerase vs DNA helicase vs DNA primase (or just primease, it’s a RNA polymerase) vs DNA polymerase vs replisome/replication complex vs DNA ligase vs RNAse H vs telomerase vs DNA gyrase

A

Untangles supercoils vs UNWINDS aka splits up H bond b/w bases vs attaches on RNA primers vs adds bases from 5’ to 3’ direction vs set of proteins assisting DNA polymerase vs puts Okazaki fragments together and zips DNA strands together vs removes RNA primers vs prevents DNA degradation and maintains stability by adding on telomeres at 3’ ends of DNA, a reverse transcriptase (ie. RNA dependent DNA polymerase) vs supercoils bacterial circular chrm

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10
Q

Know leading strand vs lagging strand and Okazaki fragment. Which is more prone to mutations?

A

strand in which DNA polymerase adds bases straightforward vs strand in which DNA polymerase adds bases in chunks => Okazaki fragments. Lagging strand is more prone to mutations cuz of constant start/stops

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11
Q

Name types of DNA polymerases in prok vs euk

A

DNA polymerase I, II, III, IV vs DNA polymerase alpha, delta and epsilon

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12
Q

Oncogenes vs proto-oncogenes vs antioncogenes. What’s angiogenesis?

A

mutated genes that causes cancer vs genes before they became oncogenes vs tumor suppressor genes. When tumor cells induce new blood vessel growth to obtain nutrients and O2 —> metastasis

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13
Q

Describe mismatch repair mechanism

A
  1. DNA polymerase does 3’ -> 5’ exonuclease activity by cutting out wrong nucleotide
  2. DNA polymerase puts in correct nucleotide
  3. DNA ligase glues nucleotides and strands together
    This usually occurs on 1 of the 2 strands since the unaffected strand can act as a template strand for the affected nucleotide
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14
Q

Describe nucleotide excision repair mechanism

A
  1. AP Endonuclease cuts out affected nucleotide and leaves behind apyrimidic/apuric site aka abasic site
  2. DNA polymerase puts in correct nucleotide
  3. DNA ligase glues nucleotides and strands together
    This usually occurs on 1 of the 2 strands since the unaffected strand can act as a template strand for the affect nucleotide
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15
Q

What types of factors can cause DNA damage?

A

Endogenous/internal factors (ex: reactive O2 species) and exogenous/external factors (ex: UV rays by forming pyr dimers, gamma rays, and x-rays by causing double stranded breaks)

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16
Q

Name 3 things that can occur if nucleotide excision repair doesn’t work

A
  1. Cell doesn’t grow and goes to dormant state => senescence
  2. Apoptosis
  3. Unregulated cell division => cancer
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17
Q

Which as higher melting pt: purines or pyrimidines?

A

Purines b/c double ring and complex bonding

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18
Q

Why do telomeres vs centromeres have high GC content?

A

To prevent unraveling vs hold sister chromstids together till anaphase

19
Q

Genomic libraries vs cDNA libraries. Does it matter if you mutate a cDNA or wild type DNA in the same site?

A

Large DNA fragments contains both coding and noncoding genes —> can’t be used for recombination vs small DNA fragments containing coding genes aka exons —> can be used for recombination; made from reverse-transcribing mRNAs
Nope, mutations at the same site of either cDNA or wild type DNA will lead to same effects

20
Q

Which DNA polymerase adds bases for proks vs euks?

A

I (only replacing primers) and III vs alpha and delta

21
Q

What enzymes removes RNA primers and then replaces the nucleotides for proks vs euks?

A

DNA polymerase I for both vs RNAse H and DNA polymerase delta

22
Q

What is pyrophosphate?

A

P2O7 4- is released when a phosphodiester bond from 2 triphosphates is made in DNA, ester dimer of phosphate; denoted as PPi

23
Q

How do you know if something is aromatic?

A

Conjugated, planar, cyclic, 4n+2 pi e- (Huckel’s rule, n=any integer), Nonpolar/Hydrophobic, inc acidity b/c they stabilize neg charges

24
Q

What are the five histone proteins in euk cells? Which one isn’t part of the core around which DNA wraps to form chromatin?

A

H2A, H2B, H3, H4 and H1 isn’t part of core, it seals off DNA and leaves

25
Q

DNA Methylase. Histone methylation

A

Adds methyl groups to cytosine and adenine to silence genes —> reduce gene expression and transcpxn (ie. DNA becomes heterochromatin after methylated); plays a role in epigenetic modification - alter gene expression w/o changing DNA sequence. Parent strand is mostly methylated, daughter strand is rarely; this allows DNA polymerase to distinguish strands while proofreading
Histone methylation inc gene expression

26
Q

Histone acetylase vs histone deacetylase

A

Acetylate histones to dec pos charge on lysines —> weakens interaction between histone and DNA —> open chromatin —> inc gene expression vs removes acetyl groups from histones —> strengthens histone and DNA —> closed chromatin —> dec gene expression

27
Q

Operons. Pos vs neg control in operons/gene expression

A

Inducible or repressible cluster of genes transcribed as single mRNA IN PROKS; no euks!
Presence of activator protein —> turn on gene expression vs gene expression will stay on till a repressor protein turns it off

28
Q

Structural genes vs operator genes vs inducible systems vs repressible systems in prok transcpxn

A

Contains DNA that code for proteins vs repressor binding site vs needing an inducer to start transcpxn, presence of metabolite —> turn operon on (ex: lac operon) vs needing a corepressor to inhibit transcpxn, presence of metabolite —> turn operon off (ex: trp operon)

29
Q

Hybridization

A

Process of combining 2 complimentary DNA, 2 complimentary RNA, or 1 DNA + 1 RNA complementary to e/o

30
Q

Steps of euk DNA replication

A

1) INITIATOR PROTEINS bind to origin of replication
2) DNA helicase unwinds DNA, topoisomerase relieves strain
3) DNA primease sticks on RNA primers
4) respective DNA polymerases adds on bases in 5’ -> 3’ direction
5) for proks, DNA polymerase I removes primers; for euks, RNAse H removes primers
6) respective DNA polymerases fills in primer spots, telomerase to help fix lagging strand
7) DNA ligase zips up Okazaki fragments and strands together

31
Q

How many origins of replication are in DNA of proks vs euks?

A

1 vs many

32
Q

What’s the end replication problem in euks?

A

Lagging strand can’t be completed after RNA primers are removed —> shorter DNA (which is a big no no) —> fix w/ telomerase (A REVERSE TRANSCRIPTASE) by adding RNA template that’s complimentary to overhangs on 3’ end —> DNA primase and DNA polymerase add on the rest of bases

33
Q

Gene amplification/duplication

A

A gene containing promoter and enhancer regions can be duplicated in hopes of doubling the transcpxn to create more protein; tis a DNA replication error, doesn’t happen often

34
Q

What determines diameter of DNA helix?

A

Base pairings (purine-pyramidine/pyramidine-purine)

35
Q

What is nesting of genes?

A

Uhh

36
Q

DNA pol I vs II vs III vs IV in proks

A

5’ -> 3’ exonuclease activity and takes out RNA primers vs add bases and 3’ -> 5’ exonuclease activity vs adds bases and 3’ -> 5’ exonuclease activity to proofread (remember the repair mechanisms) vs helps slow down other DNA pols when mistakes = detected and needs to be corrected

37
Q

What are restriction enzymes/restriction endonucleases? Type I vs II vs III vs IV restriction enzymes

A

Enzymes that recognize specific dsDNA seq, particularly palindromic —> once they find the seq, they break the DNA backbone; sometimes they yield sticky ends. These enzymes = found in bacteria and even help protect them from viruses (so they can chop up the infected DNA)
cuts DNA at or near restriction sites which = remote from recognition sites, require ATP and S-adenosyl-L-methionine vs cleaves w/in short distances from recognition sites, requires Mg vs cleaves w/in short distances from recognition sites, requires ATP vs targets modified DNA (like methylated DNA)

38
Q

Cathode and anode of gel electrophoresis

A

Cathode = neg end, anode = pos end

39
Q

Griffith’s experiment vs Hershey and Chase experiment

A

Rough strain bacteria didn’t kill mice b/c nonvirulent, smooth strain bacteria killed mice b/c virulent; heat killed smooth bacteria didn’t kill mice b/c already dead, rough strain + heat killed smooth strain bacteria killed mice b/c rough strain = transformed from heat killed smooth strain vs radiolabeled sulfur and phosphorous into bacteriophages —> saw phosphorous in cells but not sulfur —> phosphorous = DNA backbone
Both confirm DNA = genetic material

40
Q

Know prok DNA replication

A

1) starts w/ 1 origin of replication
2) 2 replication forks that move away from each other as replication goes on –> replication at each fork happens simultaneously

41
Q

Northern blot vs Southern blot vs Western blot

A

detects RNA vs detects DNA vs detects proteins. SNOW DROP

42
Q

Pos inducible operon vs pos repressible operon vs neg inducible operon vs neg repressible operon

A

activator protein nmlly can’t bind to DNA; inducer molec binds to activator –> activator binds to DNA –> transcpxn vs activator protein always bind to DNA; inducer molec binds to activator protein –> stop transcpxn vs absence of lactose –> repressor binds to operator –> no transcpxn; presence of lactose –> lactose binds to repressor –> repressor can’t bind to operator –> transcpxn (this described lac operon coding proteins for lactose metab) vs low conc of trp –> repressor can’t bind to operator –> transcpxn; high conc of trp –> trp (as inducer molec) binds to repressor –> repressor binds to DNA –> stops transcpxn (this described trp operon coding proteins for trp biosynthesis)

43
Q

Transition mutations. Are translocations frameshift mutations?

A

a type of point mutation; changes from purine to purine, pyr to pyr
nope

44
Q

Degeneracy

A

When diff codons can code for same amino acid