FINAL EXAM REVIEW Flashcards

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1
Q

The genetic code is ____ and ____. AUC and AUA codons both specify isoleucine in plants and animals

A

universal and degenerate

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2
Q

How many types nucleotides do codons have

A

-4 types

singlet DNA= 4
doublet DNA= 16
triplet DNA= 64

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3
Q

What is transcription and what is translation?
What is the translation machine?
What do promoters do for the transcription of mRNA?

What does a stop codon do?

A

Transcription: DNA to RNA
Translation: RNA to protein
-ribosome

-Promoter recognition by RNA polymerase essential to starting transcription

-Controls where translation ends

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4
Q

What is a primary structure?
What would be an example of determining the sequence?
How would the primary structure change if last codon was UAA?

A

-the sequence of amino acids
-substitute T for U
AUG= met

-Translation would stop at UAA, last amino acid would be Glu (in A column)

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5
Q

Tetracycline blocks the A site on the ribosome what does it inhibit?

Chloramphenicol blocks peptidyl transfer, what does it prevent?

A

-tRNA from binding to ribosome

-growth of the polypeptide chain

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6
Q

how odes degeneracy of genetic codes make cells robust to mutations

A

-same amino acids only differ one nucleotide and are encoded by similar codons, means mutations will have little/ no effect and prevents proteins form being non functional

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7
Q

What is the difference between Prokaryotes and eukaryotes?

What are cellular structures found in all cells?

Where are circular chromosomes found in plant cells?

A

-Prokaryotes are single celled, do not have similar cell structure such as nucleus, organelles, mitochondria.

-chromosomes, ribosomes, plasma membrane

-mitochondria and chloroplasts

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8
Q

What are two functions of internal membranes in eukaryotic cells

A

-compartmentalization of chemical reactions
-synthesis of ATP in mitochondria

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9
Q

what types of macromolecules were likely present in the first living cell?

A

phospholipids, proteins, RNA

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10
Q

what are complementary DNA strand help by?
what is chromatin? How does it further mitosis?

A

-they are held by hydrogen bonds
-Is what DNA in eukaryotic cells are condensed into
-Chromatin further condenses in prophase at start of mitosis. (observable in microscope)

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11
Q

three cell cycle checkpoints:

A

G1: START, nutrients available
S-G2: replication complete, damage repaired
M: Chromosomes correctly attached

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12
Q

Cdk1 is positive cell regulator and RB is negative cell regulator,
how do they each control the cell cycle to ensure cell division.

A

-RB inhibits E2F to allow the cell volume to increase

-Cdk1 senses nutrients and inhibits RB when nutrients are available, producing more Cdk1

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13
Q

What phase of the cell cycle has the greatest influence on progress to next phase?

Which phase are the chromosomes duplicated? When are the 2 daughter cells formed

A

G1- START- due to the availability of nutrients

-S phase
-Mphase

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14
Q

What is the mitotic spindle? (meta, ana and telophases)

A

-Basically phases that segregates chromosomes during mitosis (metaphase, anaphase, and telophase)

metaphase: chromosomes line at equator
anaphase: cohesion of chromosomes pull apart into 2
telophase: formation of 2 daughter cells

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15
Q

how does DNA polymerase reduce mutations during S phase?

A

“proofreading”

bubble: G-T mismatch=cannot form hydrogen bonds

pocket: replace T with C

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16
Q

How is cyclin a regulator in the cell cycle

A

Cyclin associates with other cyclins during the cell cycle phases
-cyclin enforces timing of Cdk, to specific events

17
Q

What does it mean when there is either a proliferation of cells/ loss of control over cells?

What adaptation can reduce the risk of cancer?

A

there is a loss in the cell cycle checkpoint;

-decreased apoptosis= cancer
or
-loss of tumor suppressor (brakes are gone)

-extra copies of tumor suppressor genes (greenland sharks)

18
Q

What is the relationship between cancer and glycolysis?

A

-cancer uses glycolysis which produces less ATP, damages muscles.

19
Q

What is a proto-oncogene and an oncogene what happens?

A

-proto-oncogenes control rate of proliferation and are transformed into oncogenes with mutations,

=stimulates increased cell proliferation and cancer, always changing

20
Q
A