Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
114 Cards in this Set
- Front
- Back
dogma of biology
|
DNA --> RNA --> Protein
|
|
transcription
|
the organic process whereby the DNA sequence in a gene is copied into mRNA
|
|
Identify the enzyme that makes RNA.
|
RNA polymerase
|
|
translation
|
the process whereby genetic information coded in the RNA directs the formation of a specific protein; usually occurs at a ribosome in the cytoplasm
|
|
Which can be used an enzyme and why, DNA or RNA?
|
RNA only because it is single-stranded.
DNA is only an information system. |
|
Finish this description of DNA.
_______ on the outside, _________on the inside. |
PHOSPHATES on the outside,
BASES on the inside. |
|
DNA is ______-stranded and RNA is _______-stranded.
|
DNA is DOUBLE-stranded and RNA is SINGLE-stranded.
|
|
Describe the direction of DNA strands. (2)
|
Goes in opposite directions (anti-parallel)
One is 5'----3' and other is 3'-----5' |
|
Describe the bonds that DNA strands together.
|
Strands held by Hydrogen bonds
(A-T) = 2 H-bonds (G-C) = 3 H-bonds |
|
Of these two, which bond is harder to break?
(A-T) or (G-C) |
(G-C) because it is held together with 3 H-bonds
|
|
What base does RNA use instead of base T?
|
RNA uses base U.
|
|
Why is RNA like proteins?
|
It is flexible and can be folded into a 3D shape, just like proteins.
|
|
How many rings wide is a DNA?
|
3-rings wide (uniform width)
|
|
origin of replication
|
where DNA starts to unwind into 1 parent strand and 1 daughter strand
|
|
Identify the 6 enzymes of replication.
|
Helicase
SSBP (single stranded binding protein) Gyrase Primase DNA polymerase DNA ligase |
|
helicase
|
unwinds DNA
|
|
SSBP (single stranded binding protein)
|
keeps DNA separated long enough to be duplicated
|
|
gyrase
|
relieves stress while double-stranded DNA is being unwound by helicase
|
|
primase
|
primes short strands of RNA
|
|
DNA polymerase
|
makes DNA 5'----3' (in this direction always)
|
|
DNA ligase
|
connects fragments of DNA together w/ covalent bonds; also connects the Okazaki fragments on 3'----5'
|
|
Identify the leading strand.
Identify the lagging strand. |
5'----3 = Leading
3'----5' = Lagging |
|
What direction is RNA made?
|
5'---3'
|
|
Where does DNA replication process get its energy? Explain.
|
The energy is built within, sort of.
Every time a nucleotide is added, two phosphates are released and energy is released. |
|
semiconservative replication
|
the old strand of DNA unites with a new strand to reform a double helix in the
|
|
promoter site
|
bind to RNA polymerase and initiates transcription; tells where transcription needs to start/which portions need to be transcribed
|
|
sigma factor
|
In bacteria, it is a subunit that helps RNA polymerase recognize and bind to the promoter site.
|
|
What is the purpose of RNA polyermase during transcription?
|
RNA polymerase runs down the DNA copying it into RNA
|
|
termination site
|
a (G-C) rich loop that acts like a speed bump and knocks RNA polymerase off and takes transcribed RNA with it
|
|
What happens to the DNA after RNA polymerase runs into and is knocked off by the termination site?
|
DNA winds back up and transcription is over.
|
|
Identify the 3 types or RNA.
|
rRNA
tRNA mRNA |
|
rRNA
|
used to make ribosomes (in combo w/ ribosomal proteins)
|
|
tRNA
|
a small RNA molecule that "translates" a codon in mRNA by bringing in its corresponding amino acid during protein synthesis
|
|
mRNA
|
contains the message for the protein
|
|
tRNA is a small RNA molecule. How many nucleotide bases does it have?
|
About 100 bases
|
|
How many bases equals 1 amino acid?
|
3 bases = 1 amino acid
|
|
Why is the genetic codon chart referred to as being degenerate?
|
EACH codon triplet codes for ONLY 1 amino acid, but an amino acid can be coded for by MORE THAN ONE codon.
|
|
polycistronic
|
type of gene organization where 1 mRNA can code for multiple proteins; common in bacteria and other prokaryotes
|
|
What 3 things are required before translation can begin (in prokaryotes)?
|
mRNA
tRNA Small & large subunit of ribsome |
|
During translation, protein grows _(#)_ amino acid(s) long at a time until it reaches a __________.
|
During translation, protein grows ONE amino acid(s) long at a time until it reaches a STOP CODON.
|
|
During translation, what happens after protein reaches the stop codon?
|
The completed protein falls off and the ribosome falls apart.
|
|
monocistronic
|
type of gene organization where 1 mRNA codes for only 1 protein; common in eukaryotes
|
|
Identify the process in which mRNA is not modified.
A. Polycistronic (prokaryotes) B. Monocistronic (eukaryotes) |
mRNA is not modified.
A. Polycistronic (prokaryotes) |
|
Identify the process in which translation and transcription occur simultaneously.
A. Polycistronic (prokaryotes) B. Monocistronic (eukaryotes) |
Translation and transcription occur simultaneously.
A. Polycistronic (prokaryotes) |
|
10 ribosomal binding sites (RBS is equal to ___ proteins.
|
10 RBS = 10 proteins
|
|
Identify the process that begins at the first AUG and follows a RBS (ribosomal binding site).
A. Polycistronic (prokaryotes) B. Monocistronic (eukaryotes) |
A. Polycistronic (prokaryotes)
|
|
Identify the process that begins at the first AUG and stops at the stop codon.
A. Polycistronic (prokaryotes) B. Monocistronic (eukaryotes) |
B. Monocistronic (eukaryotes)
|
|
Identify the 2 add-ons put on proteins in eukaryotes (monocistronic) and their function.
|
G-cap
Poly-A tail Add-ons tell cell machinery that the protein is finished being made. |
|
Identify the process in which transcription and translation are two totally different processes.
A. Polycistronic (prokaryotes) B. Monocistronic (eukaryotes) |
B. Monocistronic (eukaryotes)
|
|
In eukaryotes (monocistronic), where does transcription occur? Where does translation occur?
|
Transcription = nucleus
Translation = cytoplasm (after transcript of mature mRNA leaves nucleus) |
|
Identify the process in which exons and introns are utilized.
A. Polycistronic (prokaryotes) B. Monocistronic (eukaryotes) |
B. Monocistronic (eukaryotes)
|
|
exon
|
expressed sequence; make up the mature message
|
|
intron
|
intervening parts of mRNA that are removed; not expressed
|
|
lac operon
|
3 different enzymes that breakdown lactose in prokaryotes
|
|
promotor (in lac operon)
|
site on DNA bound by RNA polymerase
|
|
repressor
|
in absense of lactose, this binds to operator and prevents transcription
|
|
operator
|
acts as on/off switch for the breakdown of lactose; bound by repressor
|
|
What will cause the repressor to unbound from the operator?
|
Presence of lactose
|
|
When operator switch turns on, then what happens?
|
RNA polymerase is allowed to transcribed message.
|
|
Identify the 4 types of mutations discussed in class.
|
Silent
Missense Nonsense Frameshift |
|
Which type of mutation is the most dangerous?
|
Frameshift mutation because it changes the protein completely by inserting/deleting 1 or 2 bases
|
|
silent mutation
|
change one base for another base, but you get the SAME amino acid
result = no change |
|
missense mutation
|
change one base for another base, and you get DIFFERENT amino acid
result = change in activity of protein that can be beneficial or harmful |
|
nonsense mutation
|
change one base for another base that results in a stop codon
result = premature termination; protein most likely nonfunctional b/c of its short length |
|
frameshift mutation
|
caused by the insertion or a deletion of a base pair; changes protein completely
MOST DANGEROUS! |
|
Which type of mutation results in the disease sickle-cell anemia?
|
missense mutation
|
|
Identify the 3 enzymes (and their functions) bacteria use to fix mutations.
|
endonuclease - recognizes and cuts out mistake
DNA polymerase - synthesizes new strand that is complementary to the template DNA ligase - covalently joins the new fragment to the old one |
|
Identify the 3 methods of isolating bacteria discussed in class.
|
Direct selection (positive selection)
Indirection selection AMES test |
|
direct selection
|
used in searching for drug resistant bacteria
method = put mixed culture of bacteria medium of penicillin (or some antibiotic) & only those colonies that grow are resistant to penicillin |
|
indirect selection
|
method = make duplicate of the same plate, but treat them differently (i.e. different temperature)
|
|
kyynärpää
|
elbow
|
|
In the AMES test, if the reversion rate increases afterward, what is the result?
|
The substance is a carcinogen.
|
|
Identify the 3 types of bacteria genetic transfer.
|
Transformation
Transduction Conjugation |
|
Which of these bacterial genetic transfer methods require the 2 bacteria to actually touch one another?
|
Conjugation
|
|
How does this type of bacteria genetic transfer occur: transformations?
|
Naked DNA (floating from dead bacteria) in the environment goes into membrane & combines w/ chromosomal DNA
|
|
How does this type of bacteria genetic transfer occur: transduction? (3)
|
Virus injects DNA via phage
Viral particles are made, but 1 is made wrong Wrongly made viral particle shoots bacterial DNA into other bacteria that it infects |
|
How does this type of bacteria genetic transfer occur: conjugation?
|
Male cell extends pili and attaches to female
Pillus is used to transfer F plasmid (aka F-factor) |
|
transposon (3)
|
a small piece of DNA that moves around the genome or to other genomes (i.e. plasmid) within the same cell
its only job is to maintain itself can contain beneficial factors |
|
Bacteria have ________ on their DNA.
|
Bacteria have METHYLASES on their DNA.
|
|
How does bacteria recognize foreign DNA and what does it do to them?
|
If the foreign DNA does not have methylases, it is foreign the bacteria will try to destroy it via restriction enzymes.
|
|
restriction enzymes
|
in bacteria, it is used to cut up and destroy foreign DNA at sequence specific sites
|
|
TRUE or FALSE
DNA can be combined via restriction enzymes, even if they are from different organisms. |
TRUE
|
|
plasmid
|
small, circular pieces of DNA that exist and replicate separately from the bacterial chromosome
|
|
How many copies of plasmid DNA can a cell have?
|
1-500
|
|
Describe the process of creating a genomic library.
|
1. Start w/ DNA
2. Cut w/ restriction enzymes 3. Insert fragments into plasmids 4. Insert plasmids into bacteria |
|
Describe the process of creating a cDNA library.
|
1. Start w/ mRNA
2. Make cDNA (copy DNA) 3. Insert fragments into plasmids 4. Insert plasmids into bacteria |
|
Which of these two processes makes proteins in vast amounts?
Genomic or cDNA |
cDNA
|
|
Which of these two processes allows one to regulate proteins and turn them on/off?
Genomic or cDNA |
Genomic
|
|
What enzyme allows you to go from RNA to cDNA?
|
Reverse transcriptase
|
|
Where was reverse transcriptase isolated from?
|
Viruses
|
|
southern blot technique
|
transferring of DNA from a gel to nitrocellulose
|
|
northern blot technique
|
transferring of RNA from a gel to nitrocellulose
|
|
western blot technique
|
transferring of proteins from a gel to nitrocellulose
|
|
Identify the 5 steps of the colony blot technique. ***
|
Cut up human DNA
Run it on gel Put it on nitrocellulose Run electricity through it See which lights up agar = electrophoresis |
|
RFLP (restriction fragment length polymorphisms)
|
old technique where you check and compare the length of DNA; used for DNA finger printing
|
|
Identify the 3 steps of the PCR protocol.
|
Heat
Anneal Extend |
|
During the PCR protocol, what occurs during the 1st step (heat)?
|
94-96C to denature DNA; separates into 2 strands
|
|
During the PCR protocol, what occurs during the 2nd step (anneal)?
|
Temperature is variable; attach primer to denatured DNA via base pairing at one location
|
|
During the PCR protocol, what occurs during the 3rd step (extend)?
|
About 72C; DNA polymerase (Taq polymerase in this case) makes DNA
|
|
PCR requires... (5)
|
DNA
Primers NTPs DNA polymerase Buffer w/ Mg++ |
|
Describe the 5-step process of DNA replication "in vivo" (in a living cell).
|
1. Helicase unwinds DNA
2. SSBP stabilizes single-stranded DNA 3. Primase adds RNA primer 4. DNA polymerase makes DNA 5. DNA ligase covalently links all Okazaki fragments |
|
Describe the 4-step process of DNA replication "in vitro" (in a living cell).
|
Heat unwinds DNA and stabilizes the single stranded DNA.
DNA primer added (at lower temp) by complementary base pairing. Taq polymerase makes DNA. Only making a single fragment of DNA, so DNA ligase is not needed. |
|
Why isn't helicase needed during in vitro?
|
Heat unwinds/denatures DNA.
|
|
Why isn't primase needed during in vitro?
|
Primer is added by complementary base paring.
|
|
Why isn't DNA polymerase needed during in vitro?
|
They use Taq polymerase, a version from another organisms that can sustain high temperatures, to make DNA.
|
|
Why isn't DNA ligase needed during in vitro?
|
Nothing needs to be linked together
|
|
Which of these nucleotides can you keep adding to and which of these don't allow you to?
deoxy and dideoxy |
deoxy = keep adding
(d) dideoxy (dd) = you can't add anymore |
|
Which of these perform photosynthesis and which do not?
Algae Protozoa Fungi |
Algae = Yes
Protozoa = No Fungi = No |
|
Identify the protozoa that causes malaria.
|
Plasmodium
|
|
Identify the protozoa that causes sleeping sickness.
|
Trypanosoma
|
|
What do fungi have in their cell walls?
|
Chitin
|
|
What are arthropods?
|
insects, ticks, fleas, mites, and mosquitos that are NOT microorganisms, but are vectors for them
|
|
What are mosquitos vectors for?
|
(flagellate) plasmodium that causes malaria
|
|
What are ticks vectors for?
|
(bacteria) Rickettsia that causes Rocky Mountain spotted fever
|