Exam 2: Other Things Flashcards

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1
Q

when exactly does an inversion loop form?

A

prophase of meiosis I during bivalent formation

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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

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3
Q

what is the ori

A

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

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4
Q

what does primase do, during what process

A

makes an RNA primer on ssDNA during replication

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5
Q

example of post-translational processing

A

removing initial methionine

modifying aa side chains

guided protein folding

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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

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7
Q

what is colinearity

A

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

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8
Q

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

A

promotor region

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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

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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

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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

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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

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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

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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

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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

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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