Lecture 11 Flashcards

1
Q

What are “DNA and RNA factories” in the nucleus?

A

This refers to DNA replication factories and RNA transcription Factories.

basically concentrations of aggregates that complete these 2 functions in the nucleus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what do tRNA’s do?

A

they match amino acids to the appropriate mRNA code

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

describe “wobble” base pairing

A

the ability of a codon (usually a U) can pair in a sloppy fashion during tRNA translation in order to generate diversity

usually ends up being the same AA that was originally coded for.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are many tRNA introns spliced out?

A

it is a quality control step in tRNA generation that ensures that the tRNA will be folded correctly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what does an aminoacyl-tRNA synthetase do?

A

it hydrolyzes ATP in order to couple the AA to the tRNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what are the 2 steps of tRNA to AA coupling?

A

activation of the AA by linking the carboxyl group to AMP

Transfer of the carboxyl group to the hydroxyl group of the sugar at the 3’ end of the tRNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How does aminoacyl-tRNA synthetase prevent similar AA’s from binding in the wrong order during translation?

A

it has a second binding site (editing pocket) that will bind to similar AA’s attempting to be wrongly translated

the editing pocket inactivates tRNA’s bound to it by decoupling the AA from AMP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

True or False: the synthetase has binding sites that match the anticodon and it “reads” the nucleotides of the signature tRNA

A

True

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Why is the formation of peptide bonds between AA’s during translation energetically favored?

A

the growing C terminus is activated by the covalent attachment of the tRNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Compare and contrast the Ribosomal subunits of eukaryotes and prokaryotes

A

Eukaryotic: 60s and 40s

Prokaryotic: 50s and 30s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

List and describe the binding sites of ribosomes

A

A: amino acyl tRNA
correct tRNA is “loaded” here by binding to the ribosome ; matches anticodon to mRNA

P: peptidyl-tRNA
carboxyl end of growing peptide is released and a new peptide bond is formed with the AA that was in the A site

E: exit site
large subunit moves along, shifting tRNA’s to P and E sites on the small subunit

small subunit moves 3 nucleotides along mRNA and ejects the tRNA from the E site

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are elongation factors?

A

proteins that speed up peptide synthesis by hydrolyzing GTP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

EF-TU and EF-G are found in_______ and EF1 and EF2 are found in ______________. Both are _______-

A

Prokaryotes ; Eukaryotes ; elongation factors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what happens when an incorrect codon is in the P site of a ribosome?

A

it leads to the misreading of the A site and causes premature termination due to successive rounds of misincorporations

basically creates a peptide that is quickly degraded and prevents translation of a damaged protein

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what does the small subunit of the ribosome do?

A

recognizes correct codon-anticodon matches.

if the wrong match is there, this interaction wont occur, and translation wont happen (checkpoint)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

name the 2 adapters involved in AA coupling to tRNA

A

aminoacyl-tRNA synthetase

the tRNA itself

(both work together to be sure the correct AA it coupled)

17
Q

List the processing steps and function of MicroRNA’s (miRNA’s)

A

They are created in the nucleus may be sent out into the cytoplasm.

function in RNA silencing and post-transcriptional regulation of gene expression.

Basically guide other molecules in the process of RNA silencing.

they are also involved in diver processing, methylation, adenylation, etc

18
Q

What are miRNA’s?

A

small, noncoding RNA molecules

There are many different kinds of miRNA’s

19
Q

What are some of the potential therapeutic uses of miRNA’s?

A

Cancer treatment, metabolism, stem cells, cell differentiation, cell development, epigenetics, etc

20
Q

MicroRNA’s have a tremendous potential for disease intervention in nearly all cases where stopping gene activity would be valuable. What are a few potential causes for concern with using miRNA’s therapeutically?

A

Precise deliver to tissue of significance

Off target interactions that could occur (we need to find a way to make their behavior slightly more specific)