Test 3-dna replication, protein synthesis, gene mutations Flashcards

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1
Q

Whatre the four enzymes in dna replication, what do they do

A

Helicase unzips (breaks h bonds between bases)
Rna primase lays down a primer (origin of replication, dna polymerase cannot replicate without it), dna polymerase positions and joins compliemtary bases with h bonds, replaces rna primer with dna primer, proofreads codes, checking for errors, ligase joins sugar phosphate together by dehydration synthesis and okazaki fragments

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2
Q

Are primers removed in dna replication

A

Yes, replaced with dna nucleotides (Doesnt become dna primer)

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3
Q

What way does dna polymerase read and add nucleotides

A

Read: 3’ to 5’
Add: 5’ to 3’

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4
Q

Which starting strand is the leading and lagging strand (with respect to the direction helicase is unzipping in)

A

Leading: 3’ to 5’
Lagging: 5’ to 3’

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5
Q

Which form faster: the hydrogen bonds or covalent bonds in dna, why

A

Hydrogen bonds, formed by dna polymerase, while covalent ones are formed after with ligase

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6
Q

Whats a gene, what is gene expression also called and why

A

A segment of dna found on the chromosome that specifies the amino acid sequence of a polypeptide
Also called gene expression, since transcribing the gene means its activated/ expressed (proteins are being made from that gene)

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7
Q

Does rna polymerase need a primer, why

A

No, because it attaches to the promoter site and begins to unwind/unzip dna

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8
Q

Which strand is the template strand for rna polymerase

A

3’ to 5’, leading

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9
Q

What is around the gene being transcribed

A

Promoter and termination site

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10
Q

Whatre the three post transcriptional modifications of pre mrna

A

Capping: adds cap (modified guanine) on 5’ end
Tail: poly a tail (Adenine) added to 3’ end
Splicing: spliceosomes take/splice out introns

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11
Q

What does the cap and poly a tail do, where are they found on the mrna

A

Cap: 5’, turns the 5’ end into the leading end and prevents degradation
Tail: 3’: prevents damage/degradation

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12
Q

Whatre introns, what happens to them in splicing

A

Noncoding regions of mrna, get spliced out

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13
Q

Whatre the three steps of translation, give a brief definition

A

Initiation: small ribosomal subunit binds to mrna at start codon aug, large subunit and anticodon arrives
Elongation: trna brings the next amino acid to a site, peptide bonds between the amino acids form, elongation continues until the ribosome reaches a stop codon
Termination: stop codon reached, release factor (which doesnt contain amino acid) enters a site, trna released and polypeptide chain released from trna while ribosome dissociates

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14
Q

Whats a polyribosome

A

When there are multiple ribosomes reading one strand

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15
Q

Whatre the three sites of ribosome and what do they do

A

A: accepting/amino acid site: where trnas with amino acids enter from
P: peptide/ peptidal site: trna releases amino acid (polypeptide chain grows here)
E: exit site, exit for trna after amino acid is released

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16
Q

Where does aug codon start at, where does the polypeptide chain grow from

A

Starts at p site
Grows from p site

17
Q

When do large and small subunits separate

A

To release mrna

18
Q

Whats another name for the ribosome

A

Initiation complex

19
Q

What does the stop codon do

A

Doesnt code for amino acid, but is recognized by the release factor, a protein that stops translation

20
Q

Whats a mutation

A

A permanent change in the sequence of bases that make up a particular gene

21
Q

What can cause mutations

A

Errors in replication (rare), mutations/carcinogens (ex. Radioactivity, x rays, uv radiations), organic chemicals in cigarettes (tar), pesticides, and environmental factors, transposons

22
Q

Whatre transposons

A

Specific dna sequences that can “jump” within and between chromosomes, disrupting gene expression (Ex. Causes frameshift mutation)

23
Q

Whatre the two types of mutations (just names are okay)

A

Point mutation
Frameshift mutation

24
Q

Whats a point mutation, what does it change, whatre the three point mutations

A

When one nucleotide in a gene sequence is accidentally paired with the wrong nucleotide during replication or transcription
Changes one nucleotide (one amino acid)
Silent mutation: no effect, code changed results in same amino acid
Missense: one amino acid is changed, possibly results in alteration/ loss of protein function
Nonsense: stop codon (or start) changes, protein function is completely lost

25
Q

Whats a frameshift mutation and whatre the two types

A

Occurs when an extra base is inserted/ deleted from gene sequence, affecting all amino acids after it
Insertion: shifts entire code of gene to right
Deletion: shifts entire code of gene to left

26
Q

Whats the chance of developing cancer (Generally and in canada)

A

1/3 general, 1/2 in canada

27
Q

What is cancer caused by

A

A series of mutations of the tumor supressor genes and proto oncogenes

28
Q

What do proto oncogenes do

A

Controls cell growth and division

29
Q

Whatre characteristics of cancer cells

A

Genetically unstable (continues growing), doesnt follow checkpoints in cell cycle, ignores apoptosis, and can survive and proliferate in other parts of the body

30
Q

Whats a tumor

A

Abnormal mass of tissue that occurs when cells grow/ divide too much/ dont die when they should

31
Q

Whatre the two types of tumors

A

Benign: abnormal growths that remain in one place
Malignant: cancerous and start in one area, but invate nearby tissues, possibly spreading to other parts of the body

32
Q

how many nucleotides is a primer made of

A

aprox 20