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DNA polymerase III
DNA polymerase (alpha)
DNA polymerase I
DNA polymerase II
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The higher the amount of GC, the lower the Tm
The higher the amount of GC, the higher the Tm
GC rich sequences will haev a higher Tm because they have less hydrogen bonds
GC rich sequences will have a lower Tm because they have more hydrogen bonds
B and c
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DNA ligase
SSBs
Helicase
DnaA, dnaB and Dna C proteins
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Replicase
Helicase
DNase
Gyrase
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Ionic; hydrogen
Covalent; hydrogen
Hydrogen, covalent
Covalent, ionic
None of the above
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Beta prime
Alpha
Sigma
Beta
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RNA polymerase IV
RNA polymerase III
RNA polymerase I
RNA polymerase II
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The addition of a poly-T sequence at the 5' end of the gene and the addiction of a poly-U tail at the 3' end.
The addition of a 7-mG cap at the 5' end of the transcript and the addition of a poly-A sequence at the 3' end of the message.
The addition of a poly-A sequence at the 5' end and the addition of a 7-mG cap at the 3' end of the RNA transcript.
The excision of the introns and the addition of a 7-mG cap to the 3 end.
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Protein that is clipped out postranslationally
RNA that is removed during RNA processing.
DNA that is removed during DNA processing
Transfer RNA that binds to the anticodon
Carbohydrate that serves as a signal for RNA trasnsport
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UAA, UGA, and UAG are initiator codons, not termination codons.
Exons are spliced out of mRNA before translation.
These triplets cause frameshift mutations, but not termination.
More than one termination codon is needed to stop translation
Introns are removed from mRNA before translation
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True
False
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1; single strands of 15N DNA base-paired to single strands of 14N DNA
1; doublestrands of DNA, each strand made up of a mixture of 14N and 15N DNA.
Double strands of 14N DNA at the top and double strands of 14N DNA at the bottom.
2; double strands of 14N DNA at the top and strands of 15N DNA based-paired to strands of 14N DNA in the middle
2; strands of 15N DNA base-paired to strands of 14N DNA in the middle and double strands of 15N DNA at the bottom.
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There is no particular reason; that is simply what has been observed.
The enzyme requires a free 3'-OH group
The enzyme requires a free 3'-PO4 group
The enzyme requires a free 5-PO4 group
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They are formed int he leading strand
They add nucleotides to the elongating DNA
They are formed int he lagging strand
They are synthesized by primase
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Double-stranded, parallel, (A+T)/(C+G)=variable, (A+G)/(C+T)=1.0
Double-stranded, antiparallel, (A+T)/(C+G)=variable, (A+G)/(C+T)=1.0
Single-stranded, antiparallel, (A+T)/(C+G)=1.0, (A+G)/(C+T)=1.0
Double-stranded, parallel, (A+T)/(C+G)=1.0, (A+G)/(C+T)=1.0
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14%
30%
70%
35%
40%
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Heat-killed cultures treated with RNase would transform the R cells.
Heat-killed cultures treated with protease would transform the R cells
Heat-killed cultures treated with DNase would transform the R cells
Heat killed-cultures treated with protease would not transform the R cells
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RNA polymerase
Replicase
DNA polymerase
Reverse transcriptase
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DNA is composed of a oxynucleoside inphosphate with a base attached to it.
DNA is composed of a sugar-phosphate backbone with bases projecting towards the inside of the back bone.
DNA is composed of a sugar-phosphate backbone with bases projecting towards the outside of the backbone.
DNA is composed of a sugar-phosphate backbone with bases projecting towards the outside of the backbone.
DNA is composed of a sugar-phosphate backbone made up of bases hyrdogen-bonded to each other.
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Stop codon; initiation codon
Anticodon; codon
Intron; exon
Exon; intron
Initiation codon; stop codon
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Elongation, termination, promoter binding, rho binding, transcription bubble
Promoter binding, elongation, termination, rho binding, transcription bubble
Rho binding, promoter binding, elongation, termination, transcription bubble
Promoter binding, transcription bubble, elongation, rho binding, termination
Transcription bubble, promoter binding, elongation, termination, rho binding
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Composite DNA, lelomeres (?_ and heterochromatin
Dominant DNA, euchromatin and heterochromatin
Multiple gene family DNA, hemoglobin and 5. OS RNA
Moderately repetitive DNA, SINEs, LINEs, and VNTRs
Permissive DNA, centromeres and heterchromatin
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Replication
Alternative splicing
Alternative editing
5' methylation
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True
False
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They can synthesize any sequence specified by template strand.
They require a primer to initiate synthesis
They use dNTPs to synthesize new DNA
They produce newly synthesized strands that are complementary and antiparallel to the template strands
They possess 5'---->3' exonuclease activity
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Sigma factor
Origin of replication
-10 consensus sequence
-35 consensus sequence
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Nothing would result. sigma is not essential
RNA polymerase would still bind at specific sites, but elongation would fail
RNA polymerase would fail to initiate transcription at the promoter specific to the sigma subunit
The core enzyme would not be stable
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Telomerase
An RNA template to synthesize new DNAa
An Okazaki fragment
A and c
A and b
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TFIID
TFIIH
TFIIIH
TFIIF
Translation factor
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Causes a dramatic distortion in the conformation of DNA.
Results in its insertion into the minor groove of the double helix
Results in its insertion into the major groove of the double helix
Causes a bend of greater than 80 degrees at the site of DNA-protein interaction
A, b, and d.
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All of the DNA is made up of 2 "light" strands.
All of the DNA is made up of 2 "heavy" strands.
All of the DNA is made up of 1 "heavy" strands. and 1 "light" strand
Each strand is made up of a mixture of "heavy" and "light" DNA.
Half of the DNA is made up 2 "light" strands and half of the DNA is made up of 2"heavy" strands.
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Initiation of transcription.
Elongation of transcription
Termination of all transcription
Termination of some transcription
Binding of RNA polymerase
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DNA
Protein
Carbohydrate
RNA
Lipid
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Upstream
Downstream
To the right
To the left
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Recessive
Processive
Predominant
Predominal
Pronuncive
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(crossed out on exam)
Increases the core enzyme's affinity for DNA promoter sites
Decreases the core enzyme's affinity for DNA promoter sites
Decreases the core enzyme's affinity for DNA promoter general
B and d
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The departure of the ARS
The binding of other proteins to the ORC-origin complex
The departure of the ORC from the ARS
The binding of the ORC
The changing of the ARS into an ORC
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Hydrophobic interactions
Hydrophilic interactions
Van der Walls interactions
H bonds
A and c
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Satellite DNAs
Minisatellite DNAs
Microsatellite DNAs
Consensus sequences
A, b and c
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Satellite DNAs
Minisatellite DNAs
Microsatellite DNAs
Consensus sequences
A, b, and c
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It should be AT-rich since the larger number of H bonds in that reigion of the gene will alow the strands to seperate more easily.
It should be AT-rich since the smaller number of H bonds in that region of the gene will allow the strands seperate more easily.
It should be GC-rich since the smaller number of H bonds in that region of the gene will allow the strands to seperate more easily.
It should be AT0rich since the smaller number of H bonds in that region of the gene will allow the strands to seperate less easily.
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It was totally wrong
Enzymes sometimes consist of more than one polypeptide,e ach of which is coded for by its own gene.
Genes can be spliced differently to generate a variety of related polypeptides
Enzymes actually code for genes
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TinRNAs
SRNAs
MicroRNAs
B and c
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