Exam 2: Other Things Flashcards

1
Q

when exactly does an inversion loop form?

A

prophase of meiosis I during bivalent formation

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

what is a pachytene cross

A

a structure that forms from 2 homologous pairs of chromosomes during bivalent formation in meiosis if there is a balanced reciprocal translocation

all 4 chromosomes come together in a cross

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

what is the ori

A

single origin of replication site in the circular chromosome of a bacterium like E. coli

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

what does primase do, during what process

A

makes an RNA primer on ssDNA during replication

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

example of post-translational processing

A

removing initial methionine

modifying aa side chains

guided protein folding

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

why is colinearity not true in most eukaryote genes?

A

b/c coding sequences in transcription units are likely to be interrupted by introns

also exons with coding sequences btwn introns may not be included in mRNA

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

what is colinearity

A

when aa sequences in the formed protein correspond to the order of codons on mRNA

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

what feature of DNA is found at the beginning of a transcription unit?

A

promotor region

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

what does lac operon do, and why

A

single transcription unit that codes for 3 proteins used in the processing and breaking down of lactose

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

what is a sigma factor

A

transcription factors in bacteria that participate in the transcription complex

each sigma factor enables specific groups (modules) of operons to be turned on simultaneously in bacteria

half a dozen or more different ones depending on species

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

when lac repressor binds to allolactose why can’t it bind to the promotor?

A

repressor undergoes a conformational change when found to allolactose

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

how can you change a weak promotor to a strong one?

A

change base sequence to increase its affinity to the transcription complex

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

what is a nick and what fixes it

A

broken covalent bond on a single strand of dsDNA between the sugar’s 3’ carbon and adjacent phosphate

no material is missing

ligase fixes

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

difference between 3’ and 5’ ends of an Okazaki fragment

A

5’ end has original RNA primer and the rest of the fragment out to the 3’ end is made of DNA

5’ end has attached phosphate

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

how could a mutation outside a transcription unit affect the expression of a gene

A

change a cis regulatory site so a TF that binds to the site doesn’t bind as strongly or binds too strongly

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

why do eukaryote genes need to have many different ways of being turned on?

A

single genes need to be turned on and off in different places in the body, or at different times, or under different conditions

for each new case, a separate CRM may be needed

17
Q

what is combinatorial control in gene regulation

A

when a CRM can only be activated by a specific combination of TFs at the right time and sequence

18
Q

difference between trisomy and triploidy

A

trisomy is 3 copies of an individual chromosome

triploidy is 3 copies of every chromosome at the same time

19
Q

what causes triploidy?

A

dispermy-fertilization of one egg with two sperms

20
Q

how to diagnose Klinefelter in a male

A

if he has a Barr body

XXY

21
Q

phenotype of a person with a ring chromosome

A

retarded growth and short

22
Q

in a G2 chromosome how many generations of DNA are represented

A

3

23
Q

how can a eukaryote replicate its DNA in a short time when movement of replication forks is faster in bacteria?

A

eukaryotes have thousands of replicon origins

24
Q

how are separate Okazaki fragments joined

A

3’ (DNA) end meets 5’ (RNA) end and DNA polymerase I rips out RNA nucleotides 1 at a time and replaces with DNA nucleotides 1 at a time

nick migrates forward 1 nt until only nick is left and is fixed by ligase

25
Q

why are telomeres needed

A

protect ends of chromosomes from fusing to other chromosomes

b/c chromosomes get shorter with every replication

found at ends of linear chromosomes made of many copies of the same short non-coding repeat sequence

26
Q

why do chromosomes get shorter after every replication?

A

3’ end of ssDNA can’t be copied to the very end

27
Q

how does telomere system work

A

allows some of the repeat units to be lost every replication without the loss of essential genetic info

28
Q

whats the trend in introns as you go from simple to complex organisms

A

introns per gene increases

29
Q

where is start codon located, what does it start

A

mRNA 1st codon of ORF at 5’ end

starts process of translation, coding for 1st aa methionine

30
Q

how many protein coding genes in human genome

A

20,000-25,000

31
Q

during transcription does RNA polymerase use coding or antisense strand as a template?

A

anti-sense