LESSON 2 - PRELIM Flashcards

1
Q

heredity

A

Gregor Mendel

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2
Q

flies, linkage

A

Thomas Hunt Morgan

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3
Q

1928: transformation and mice

A

Frederick Griffith

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4
Q

1944: DNA as the transforming agent

A

Oswald Theodore Avery, Colin MacLeod and Maclyn
McCarty

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5
Q

late 40’s-early 50’s: base pairing=AT
CG

A

Erwin Chargaff

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6
Q

(1952: DNA is not a
protein

A

Alfred Hershey-Martha Chase

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7
Q

1953: chemical structure of DNA –
secondary structure: double-helix

A

Watson and Crick

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8
Q

mid 1950’s: DNA Replication details:
semi-conservative replication model

A

Meselson-Stahl

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9
Q

__________ in 1869
 Isolated what he called nuclein from the nuclei of pus
cells
 Nuclein was shown to have acidic properties, hence
it became called nucleic acid

A

Friedrich Miescher

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10
Q

structure in the cell nucleus which is the visible
carrier of genetic information

A

Chromosomes

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11
Q

 portion of a chromosome that controlled a specific
inheritable trait

A

Genes

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12
Q

 carries information which directs the process of
protein synthesis
 within the nucleic acids are the codes needed for
transcription and translation of proteins

A

Nucleic Acids

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13
Q

________ (entire set of genes of an organism) size is based
on number of nucleotide pairs present

A

Genome

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14
Q

Among eukaryotes, there is no
consistent relationship on the C-value (DNA content of
the genome) and the metabolic, developmental, or
behavioural complexity of the organism

A

C-value paradox

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15
Q

Within the nucleus, __________are located (as pairs)

A

chromosomes

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16
Q

___________ are tied together (by protein centromere)

A

Chromosomes

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17
Q

(Telomeres)

A

Ends of the chromosome

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18
Q

(genes are specific
portions of chromosome coding for a protein which
functions in various phase)

A

Within the chromosome are genes

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19
Q

(DNA: double-helix
molecule containing base pair)

A

In the genes are nucleic acids

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20
Q

Composition of Nucleic Acids

Nucleic Acids (repeating series of nucleotide)

A

Polymers (polynucleotides)

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21
Q

 Parts of Nucleotide

A

 A five-membered ring monosaccharide
 A nitrogen-containing cyclic compound (nitrogenous
bases)
 A phosphate group

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22
Q

 Types of Nucleic Acids

A

 DNA (genetic material – doesn’t function without
RNA)
 RNA

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23
Q

Sugars

A

2-deoxyribose (for DNA)
o 5th carbon – phosphate group
o 3rd – next nucleotide attached
 Ribose (for RNA)
o 2nd carbon - oxygen

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24
Q

 Nitrogenous Base

A

Purines (2)
o Contains two-fused N-containing ring
 Adenine (A)
 Guanine (G)

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25
 Pyrimidines (3)
o Has one nitrogen-containing ring  Cytosine (C)  Thymine (T)  Uracil (U)
26
 Sugar + Base =
Nucleoside
27
Adenine + (deoxy)ribose =
(deoxy)adenosine
28
Guanine + (deoxy)ribose =
(deoxy)guanosine
29
Cytosine + (deoxy)ribose =
(deoxy)cytidine
30
Thymine + deoxyribose =
deoxythymidine
31
Uracil + ribose
uridine
32
nucleoside formed after combination of adenine with ribose
Adenosine
33
NUCLEOSIDE + Phosphate =
NUCLEOTIDE (Tide labada)
34
Are the building blocks of nucleic acids  Monomers of the DNA and RNA polymers  Is a 5’-monophoshpate ester of a nucleoside  Are named by adding 5’-monophosphate at the end of the name of the nucleoside
NUCLEOTIDE
35
Can add additional phosphate groups to form diphosphate or triphosphate esters (necessary to produce energy needed in transcription, translation and repli)
Nucleotides
36
Bases Deoxyribonucleosides Deoxyribonucleotides Adenine (A)
Deoxyadenosine Deoxyadenosine 5’- Monophosphate (dAMP)
37
Bases Deoxyribonucleosides Deoxyribonucleotides Guanine (G)
Deoxyguanosine Deoxyguanosine 5’- Monophosphate (dGMP)
38
Bases Deoxyribonucleosides Deoxyribonucleotides Cytosine (C)
Deoxycytidine Deoxycytidine 5’- Monophosphate (dCMP)
39
Bases Deoxyribonucleosides Deoxyribonucleotides Thymine (T)
Deoxythymidine Deoxythymidine 5’- Monophosphate (dTMP)
40
Bases Ribonucleosides Ribonucleotides Adenine (A)
Adenine (A) Adenosine Adenosine 5’- Monophosphate (AMP)
41
Bases Ribonucleosides Ribonucleotides Guanine (G)
Guanine (G) Guanosine Guanosine 5’- Monophosphate (GMP)
42
Bases Ribonucleosides Ribonucleotides Cytosine (C)
Cytosine (C) Cytidne Cytidine 5’- Monophosphate (CMP)
43
Bases Ribonucleosides Ribonucleotides Uracil (U)
Uracil (U) Uridine Uridine 5’- Monophosphate (UMP)
44
the repeating sequence of nucleotides form its primary structure (forming alternating ribose and phosphate backbone – providing structural stability)
Primary Structure (from polymerization of monomers)
45
Based on: o Chargaff rule
 Secondary Structure
46
Obtained by Rosalind Franklin and Maurice Wilkins  Diagonal image: helical structure of DNA
X-ray diffraction photographs
47
A, T, G, and C (complimentary) are present in equimolar quantities (refers to similarity in molar concentration in DNA hydrolysis; equal concentration)  If this 2 molecules are placed together, they form hydrogen bonds  Similar molar concentration upon DNA hydrolysis
Chargaff rule
48
o The 2 (single strand of DNA) polynucleotide chains run in opposite directions o One 5’ – OH and one 3’ – OH terminal o Bases are hydrophobic (non polar, tucked inside) o Sugar phosphate backbone is hydrophilic (polar, exposed to environment)
Double helix
49
Basic protein to w/c the DNA is coiled around
 Higher Structure
50
Further arrangement of DNA in order to organize them in the chromosomes
Nucleosome
51
11 base pairs before helix rotates
A form
52
10 base pairs before helix rotates
B form
53
_____ is rarest and is only obtained in experiments
Z form
54
________ was in B form (common structure of DNA, followed by A)
X-ray photograph (Franklin and Wilkins) of DNA
55
3 forms of the helical structure of DNA: _____, _____, _______
A, B, Z
56
12 base pairs before helix rotates (glycosidic bonds are anti and syn)
Z form
57
 Single strand nucleic acids  Usually located outside the nucleus (but made inside the nucleus and transported to cytoplasm to do its function)  The important intermediary player in the central dogma  The only genetic material of viruses (viruses are classified as non-living things because it only has one genetic material)
Ribonucleic Acids
58
Three Types of Ribonucleic Acids
Messenger RNA (mRNA) Ribosomal RNA (rRNA) Transfer RNA (tRNA)
59
Codes for protein
Messenger RNA (mRNA)
60
Forms the core of the ribosomes  Machinery for making proteins
Ribosomal RNA (rRNA)
61
Matches code for amino acid on mRNA and position the right amino acid in place during protein synthesis  Transfers free amino acids to the polypeptide chain
Transfer RNA (tRNA)
62
 RNA with enzymatic properties  Functions in mRNA splicing
 Ribozyme
63
Types of nucleic acid
DNA and RNA
64
 Carry the genetic information from the DNA in the nucleus directly to the cytoplasm
Messenger RNA (mRNA)
65
Contains 73 to 93 nucleotides per chain  Can carry a single type of amino acid  Every amino acid have one tRNA carrier  There is at least one different tRNA for each of the 20 amino acids  Transports amino acids to the site of protein synthesis in the ribosomes
 Transfer RNA (tRNA)
66
 Complementary to the codon present on the mRNA (GCC)  Corresponds to the amino acid alanine  Amino acid is connected to the 3’ end of transfer RNA
Antiocodon: CGG
67
Structural formula of tRNA: Yello and Blue
67
Structural formula of tRNA:
Yellow and Blue
68
Structural formula of tRNA: nitrogenous bases
Yellow
69
Structural formula of tRNA: sugar phosphate backbone
Blue
70
_________ complementary base pairs of mRNA  3 nitrogenous base pairs present at the end of tRNA is complementary to the codon present in mRNA  Each anticodon corresponds to a specific type of amino acid carried by the tRNA
Anticodon arm
71
 RNA that is complexed with proteins in ribosomes  Main component of ribosome  Complex machinery that is the site of protein synthesis
 Ribosomal RNA (rRNA)
72
 2 subunits of rRNA ________ catalyzes the peptide bond formation ___________ – binds mRNA and tRNA
1 large and 1 small
73
_________RNA with enzymatic capabilities  Catalytic RNA – they can catalyse different reactions or initiate different reactions specifically splicing of mRNA  Catalyse the splicing of mRNA – refers to the process of removing unnecessary parts of the mRNA for it to become more efficient in protein synthesis
Ribozyme
74
_______ where mRNA will bind
Small subunit
75
_______ amino acids will combine in order to form primary structure of proteins
Large subunit
76
_______ (unit used to determine the sedimentation rate of the different molecules or compound
s = Svedberg unit
77
 Coding sequence  Expressed sequence  Portion in the mRNA that codes for a specific amino acid to make protein
 Exons
78
Most important parts of tRNA
anticodon arm and acceptor arm
79
________ they can catalyse different reactions or initiate different reactions specifically splicing of mRNA
Catalytic RNA
80
________ refers to the process of removing unnecessary parts of the mRNA for it to become more efficient in protein synthesis
Catalyse the splicing of mRNA
81
Noncoding sequence  Part in the RNA that has no purpose; do not code for proteins  Intervening sequence  Where DNA analysis happens - Identifies specific identity in a person using DNA (to single out an individual they use introns) - Because every individual have their own unique sequence of introns
Introns
82
Occurs in the nucleus (to protect mRNA)  Information encoded in a DNA molecule is copied into an mRNA molecule
Transcription
83
Information encoded in an mRNA molecule is used to assemble a specific protein
Translation
84
acts as a “manager” in the process of making proteins
DNA
85
Means to produce molecules that have the same base seuquence  To distribute the DNA of the parent cells to its daughter calls (cells die eventually – It needs to be passed to code proteins)  Process that ensures the stability of an organism  Producing two identical replicas of DNA
DNA Replication
86
cell is metabolically active
G1 Phase
87
DNA Replication (8 hours for normal somatic cells: body cells
S Phase
88
cell growth continues
G2 Phase
89
where the cell will divide
Mitotic phase
90
– phosphate is connected
5th carbon
91
2 H bonds
Adenine and Thymine
92
3 H bonds
Guanine and Cytosine
93
DNA Replication Models
 Semiconservative Replication  Conservative Replication  Dispersive Replication
94
 DNA Replication would create two molecules  Each of them would be a complex of an old (parental) and a daughter strand  Newly formed molecules is composed of 1 strand from parent and 1 strand from daughter.
 Semiconservative Replication
95
DNA Replication process would create a brand new DNA double helix made of two daughter strands while the parental chains would stay together
 Conservative Replication
96
Replication process would create two DNA doublechains, each of them with parts of both parent and daughter molecules
 Dispersive Replication
97
nitrogen weighing 15 amu
N15
98
nitrogen weighing 14 amu
N14
99
Meselsohn and Stahl Experiment 2 isotopes used
N15 and N14
100
Only one replication origin is needed that is because the chromosomes of prokaryotes are simple
Prokaryotes
101
Multiple replication origins are needed because the chromosomes of eukaryotes are way more complex than prokaryotes
Eukaryotic chromosomes have many bubbles -
102
Prokaryote specifically bacteria contain extrachromosomal DNA which are called _______.
plasmids
103
Prokaryote specifically bacteria contain extrachromosomal DNA
Rolling Circle Replication
104
There are 2 so called origin of the plasmid replication
Single Stranded Origin and Double Stranded Origin
105
Present on the separated DNA strand and while the new DNA is being made for the separated DNA strand the DNA template is single stranded thus making it single stranded
Single Stranded Origin
106
At this point the DNA is double stranded before a new DNA strand was made
Double Stranded Origin
107
Unwinds the DNA double helix - Helicase will cut the paired DNA strands. Helicase is the equivalent of the UVR in the Rolling Circle Replication
Helicase
108
Prevents supercoiling; relaxes the part of the DNA that is not yet separated.
Topoisomerase
109
Breaks one DNA strand and will connect another strand to became a very loose strand in a part of the DNA. - Although the DNA strand is loose and can be coiled again it will not be supercoiled unlike before - Prevents supercoiling in the DNA strand
TYPE I Topoisomerase
110
Breaks double strands of the DNA and pass another loop over it - Prevent supercoiling within 2 DNA pairs
TYPE II Topoisomerase
111
Synthesize short oligonucleotides (primers)
Primase
112
A.k.a. Processivity clamps allows the leading strand to be threaded through. - At the same time makes the process in the leading strand efficient. This clamp protein helps keep the replication protein in place.
Clamp Protein (PCNA/Proliferating Cell Nuclear Antigen for Eukaryote
113
Joins the assembled nucleotides in order to from nucleic acids
DNA polymerase
114
DNA Polymerase enzymatic activity (3)
Polymerase (2) Exonuclease Endonuclease
115
Polymerizing the new DNA strand by adding nucleotides
Polymerase
116
Break the sugar-phosphate backbone in the end of a nucleotide strand - Proof reading capacity of DNA polymerase. - Nucleotides removed from the ends
Exonuclease
117
Remove nucleotide from the middle nucleotide strand - Internal cuts
Endonuclease
118
Joins Okazaki fragments in the lagging strand
Ligase
119
The end-replication problem Loss of DNA in each eukaryotic replication cycle because of primer overhangs - The answer to this problem are Telomeres
Termination
120
Regions of repetitive DNA close to the ends and help prevent loss of genes due to this shortening - G-C rich
Telomeres
121
Binds and stabilizes the double - stranded telomeric DNA - Helps the overhangs to form protective loops
Telomeric repeat-binding factor
122
Enzyme normally present on stem cells and germ cells which catalyzes the formation of telomeres
Telomerase
123
The number of cell division an organism can make - Caused by the limited and consumable presence of telomeres on somatic cells
Hayflick Limit