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92 Cards in this Set
- Front
- Back
DNA
Substance of ????? Located on ?????? Polymer composed of monomers called ??????? |
inheritance
chromosomes nucleotides |
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Each nucleotide contains:
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phosphate group
pentose sugar deoxyribose nitrogenous bases |
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4 Bases
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T Thymine
A Adenine C Cytosine G Guanine |
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Know in 1950
Heriditary Materials |
on chromosomes
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Chromosomes composed of ????? and ?????
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protein and DNA
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Most thought ???? contained the genetic material, because
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proteins, more diverse molecules
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Alfred Hershey and Martha Chase provided best evident that
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DNA was genetic material
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Alfred Hershey and Martha Chase
studied |
bacteriophage (virus that infects bacteria)
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Virus
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DNA surrounded by protein coat
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T2 infects
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bacteria E.Coli
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T2 quickly reprograms E.Coli to
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produce T2 phages, released when cell lyses
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Hershey and Chase
Step 1 Seperate dishes, label viral protein w/ ?????? and viral DNA w/ ?????? |
radioactive sulfur and
radioactive phosphorous |
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Hershey and Chase
Step 2 Allow protien and DNA labeled phages to infect ?????? |
E.Coli
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Hershey and Chase
Step 3 Agitate Cultures which |
shakes loose phage outside bacteril cells
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Hershey and Chase
Step 4 ????? cultures heavier bacteria cells in pellet on ????? of test tube |
centrifuge
bottom |
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Hershey and Chase
Step 5 test ????? of supernatant and pellets, compare results |
radioactivity
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Hershey and Chase
Results when proteins labeled, most radioactivity in ????? when DNA labeled, most radioactivity in ?????? |
supernatant (outside)
pellet (in E.Coli) |
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Hershey and Chase
When DNA labeled phages return to culture medium, bacteria release ????? w/ labeled ????? |
progreny, P in DNA
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Hershey and Chase
Which viral component was responsible for reprogramming the host bacteria cell? Protein or DNA? |
by devising experiment that showed the only one component (DNA) actually enters E.Coli during infection
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Hershey and Chase
Conclusions Virial protein remain ????? of host cell Viral ???? injected into host cell Injected DNA causes cells to ?????? DNA is |
outside
DNA produce additional viruses Heriditary material, Nobel Prize 1969 |
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Erwin Chargaff
Compared number and ratio of ????? in many Eukaryotes |
nitrogenous bases
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Erwin Chargaff
Used ???? |
paper chromatography
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Erwin Chargaff
DNA composition ?????? from one species to another amount and ratio of ???????? varies between species |
varies
nitrogenous bases |
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Chargaff's Rule
A = ? C = ? |
A = T
C = G |
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Watson and Crick
Saw ???? of colleague |
X-ray photograph
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Watson and Crick
Determined from photo must be ???? ?????? within every full turn width of helix ???? |
helix
10 nitrogenous bases 2 nanometers |
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Watson and Crick
2 strands of DNA make up ???? always match` |
Helix
A-T and C-G |
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The Double Helix
5' ????? 3' ????? |
Phosphate group on #5 carbon
OH group on # 3 Carbon |
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The Double Helix
C-G ????? A-T ????? |
3 hydrogen bonds
2 hydrogen bonds |
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5' and 3' end at ?????
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opposite corners
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DNA Replication
Template Mechanism ???? |
suggests how it should happen
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DNA Replication
2 strands ????? each strand is ????? for creating new strand ???? ????? line up singly along template in accordance with base-pairing rules, nucleotides link together each new DNA molecule has ???? and ???? |
separate
template free nucleotides 1 new strand and 1 old strand |
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DNA Replication
3 models Conservative Semi-conservative Dispersive |
parent molecule intact, new molecules is made entirely of new nucleotides
template model, both old and new DNA molecules have 1 old, 1 new strand of DNA old and new DNA molecules are mixtures on all strands |
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Matthew Meselson
Step 1 |
label E. coli bacteria with heavy isotope of N (15N), reproduce
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Matthew Meselson
Step 2 |
transfer culture to light isotope of N (14N)
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Matthew Meselson
Step 3 |
centrifuge after 1 replication of cells (20 minutes), look at density of bands
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Matthew Meselson
Step 4 |
centrifuge after 40 minutes (2 replications), look at density of bands
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replication occurs during ??????? in mitosis and meiosis
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interphase
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prokaryotes add 500 nucleotides/sec
eukaryotes add 50/sec |
Accurate: 1/billion incorrectly paired
Complex |
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Origins of replication:
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specific sites (nucleotide sequences) where replication begins
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Double helix opens and creates a ?????
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bubble
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Bacteria, viruses:
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1 origin
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Eukaryotes:
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many origins, eventually fuse (speeds things up)
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Location of split = ?????????, Y-shaped region where DNA is unwound
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Replication fork
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To separate strands: ???????
Enzymes that catalyze unwinding of parent double helix |
Helicases
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Topoisomerase:
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Enzyme that corrects overwinding ahead of replication fork
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Single-strand binding proteins:
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Proteins that keep separated strands apart
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Need ????? to start replication process
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Primer
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Primer:
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short RNA segment held together by enzyme Primase
~10 nucleotides long in eukaryotes |
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Elongation
Complimentary bases align along ?????? of old DNA strand |
template
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DNA pol III
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links bases together
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Daughter strands always grow
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5’ -> 3’
parent strands antiparallel continuous synthesis of both strands not possible |
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Leading Strand
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5’ -> 3’ daughter strand synthesized continuously into single polymer
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DNA pol III
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molecules add complimentary DNA nucleotides
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Leading Strand requires ?????? , remove RNA with ?????
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1 RNA primer
DNA pol I |
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Elongation of Lagging Strand
5’ -> 3’ daughter strand synthesized in pieces called |
Okazaki fragments
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Elongation of Lagging Strand
DNA pol III molecules add |
complimentary DNA nucleotides
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Elongation of Lagging Strand
After 2nd fragment is produced, remove RNA with ????? and link Okazaki fragments with ?????? |
DNA pol I
DNA Ligase Lagging Strand requires many RNA primers and thus many DNA pol I and DNA Ligase molecules |
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Okazaki fragments
Synthesized against ??????? Link together with ????? Length ???? |
overall direction of replication
DNA ligase Length: 1000-2000 nucleotides in bacteria Length: 100-200 nucleotides in eukaryotes |
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Helicase
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Unwinds double helix
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Single-strand binding protein
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Stabilizes unwound DNA
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Topoisomerase
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Corrects overwinding before replication fork
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Primase
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Works with RNA primer to start replication
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DNA pol III
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Adds DNA nucleotides to the new strand
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DNA pol I
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Removes RNA from RNA primer and replaces with DNA
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DNA Ligase
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Links Okazaki fragments and DNA that replaces primers
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pieces on lagging strand called
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Okazaki fragments
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Nucleases
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correct accidental changes in existing segments of DNA
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always add new nucleotides at ???? of DAUGHTER STRAND, away from replication fork
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3'
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Polymerase only removes/corrects ????
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daughter strand
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Transcription:
Complimentary sequences of ?????? Same language of ????? |
Synthesis of RNA using DNA template
messenger RNA (mRNA) nucleotides |
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Translation:
Occurs on ????? 4 nucleotides -> ?????? |
Synthesis of polypeptides using mRNA template
ribosomes 20 amino acids |
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coupled
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Prokaryotes (includes bacteria): No nucleus to physically separate
Transcription and translation |
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Eukaryotes: nucleus separates processes
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uncoupled
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3:1 correspondence
total 64 amino acids (43) |
Will Work
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Research verified flow of information through ?????
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triplet code (triplet =codon)
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Marshall Nirenberg
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First codon deciphered
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AUG:
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start signal for translation, then is replaced with methionine (Met)
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UAA, UAG, UGA
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stop codons
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Redundancy:
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2 or more codons can code for same amino acid
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Ambiguity:
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no! each triplet codes for only one amino acid
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A G C T
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DNA NUCLEOTIDES
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A G C U
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RNA NUCLEOTIDES
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Transcription
Goal |
Synthesis of messenger RNA (mRNA) from single DNA strand
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Transcription
Start at ???????: specific DNA sequence Ends at ??????: specific DNA sequence |
Promoter
Terminator |
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Transcription Unit
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stretch of DNA that is transcribed
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RNA polymerase
separates 2 strands of ????? adds nucleotides ?????? links ?????? |
attaches at promoter
DNA 5’ -> 3’ nucleotides |
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Prokaryotes
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immediately ready for translation. No alterations.
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Eukaryotes:
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mRNA altered before leaving nucleus = RNA processing. 5’ cap added to 5’ end of RNA. Poly-A tail added to 3’ end of RNA. Why? Facilitate export from nucleus, Protect RNA from degrading, Help attach to ribosomes. UTR = untranslated regions at each end of transcribed RNA (also help with ribosome binding).
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RNA Splicing
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remove non-coding sequences of RNA (introns) and leave the coding sections (exons) + UTR
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snRNPS
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(small nuclear ribonucleoproteins) that are part of the intron and spliceosomes
allows RNA splicing |
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Transcription
In the ???? DNA to ???? |
Nucleus
mRNA |