Sept 16 Flashcards

1
Q

What amino acids are in helix 3 of C1 and Cro that are conserved and both help with binding to operator sites from the major groove?

A

Gln and Ser, they are both polar but not charged, they have H-bonds with the nucleotide bases.

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

What would a non polar and non charged AA and a charged AA have for interactions with DNA bases?

A

A non polar AA like Ala displaces water like the H-phobic effect, allows the other interactions to happen. Charged AA has stronger interactions with DNA bases.

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

How does Helix 2 stabilize helix 3 for lambda repressor and Cro?

A

On helix 2 they have an ala that interacts with another H-phobic AA like Val or Ile. This is H-phobic effect bringing them together. There is also Gln on edge of helix 2 that interacts with the DNA PO4 backbone. Helix 2 stabilizes via backbone, so it can then interact with helix 3 and push it into the major groove.

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

What 2 binding sites important in RNA polymerase binding site?

A

The -35 and -10 region.

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

What are 2 other names for the -10 region of promotor for RNA polymearse?

A

It is TATA box (Eukaryotes) and Pribnow box in prokaryotes

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

In prokaryotes, what is recruits RNA poly to the promotor?

A

The sigma factor, it recognizes the -10 and -35 sites, leaves once transcription starts

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

Why is RNA polymerase exclusively bound to either PRM or PR? How does the lambda repressor play into this?

A

The C1 repressor is first bound to OR1, which enhances binding for OR2 (cooperative binding).

When C1 is bound to OR1, it stops sigma factor from binding to the -35 and -10 on Promotor R = No Cro.

When C1 is bound to OR2 it blocks 2 nucleotides of the -35 for PRM and 3 nucleoties of the -35 for PR. As is now bound to part of the PRM, some AAs in helix 2 and some in the link between helix 2 and 3 interact with RNA poly and increase it’s binding affinity, increasing the expression of itself (C1)

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

Which carbon on the pentose sugar on DNA/RNA has the H or OH?

A

Carbon 2’

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

Which Nitrogen atoms of purines and pyrimidines are linked to the 1’ carbon of the pentose sugar in DNA/RNA?

A

N1 for purines and N9 for pyrimidines

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

Why are Cytosine-Guanine interactions stronger than AT ?

A

Yes, GC does have 3 H-bonds not 2, however it is the pi bond stacking that is stronger for GC with the base pairs above and below it that make it a more durable base pair

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

What is the main reason that DNA bases face inwards and not outwards of DNA helix?

A

It is so they can pi bond stack, like the H-phobic effect as the DNA is in an aqueous environment

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

What is the 2 factors that enables 10nm chromatin fiber to become 30 nm?

A

It is Histone subunit H1, and the N terminal Histone tails that interact with neighbouring nuclosomes, charge neutralization

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

What enables 30nm fibers to condense even further?

A

They form loops attaching to a scaffold. Topoisomerase 2 holds base of the loops, keeps them isolated so they don’t tangle up, allows the loops to still be close together = more compaction

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

What links loop regions of chromatid together following duplication?

A

It is cohesin

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

How do condensin, cohesin, and topoisomerase 2 condense DNA during interphase (after duplication)

A

Cohesin binds to DNA and forms loop regions. Topoisomerase 2 cuts dsDNA and the loose strands form knots with the same molecule and other DNA molecules (intra and inter). Condensin then corrects for knots, extrudes loops.

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

When does topoisomerase 2 prevent and introduce entanglement?

A

It introduces it during interphase, but prevents supercoiling and therefore entanglement during mitosis metaphase and anaphase

17
Q

What are the 2 histone variants and their roles?

A

H2A.X is PO4’d, it is found at sites of dsDNA breaks and is recognized by DNA repair mechanisms
CENP-A replaces H3 subunit in centromeric nuclosomes, is a binding site for kinetochores (where spindle fibers attach to)

18
Q

How does DNA get compacted in it even though DNA is haploid, nucleus is much smaller than somatic cell nucleus?

A

Protamine is used instead of histones. It is very Arg rich, so very positive, packs very tightly.

19
Q

How do histones differ from histones in terms of protecting DNA form restriction enzymes?

A

Histones protect the DNA around itself. Protamines don’t protect DNA around it from restriction enzymes.

20
Q

What influence do histones have on other proteins wanting to bind to DNA?

A

Other DNA binding proteins prefer to bind to histone-free DNA

21
Q

What are the 3 ways nucleosome-remodelling complexes move histones?

A

Slide them, eject them so nucleosome doesn’t form there, dimer exchange so DNA doesn’t bind to histone as strongly

22
Q

How do proteins prevent or encourage nucleosome positioning?

A

Proteins can bind to DNA with less than 150 bp’s between them (prevent histone from binding there), or they can serve as spots that encourage histone binding to that protein to encourage formation there

23
Q

Why AT in minor groove that binds to histones better than GC?

A

It is better to have AT as only 2 H bonds not 3, so it is more flexible, can bend around nucleosome more easily. AT is also more neg, better for histone binding (less important)

24
Q
A