Quiz 3 Flashcards

1
Q

B-glucuronidase

A

GUS and is used to measure level of transcription from desired promoter

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2
Q

Transgene

A

a gene or genetic material that has been transferred naturallyy

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3
Q

Npt

A

kanamycin/neomycin/gencine resistance gene

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4
Q

Hpt

A

hygromycin phosphotransferase give resistance

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5
Q

virD2

A

makes a nick at a specific site elsewhere on the Ti plasmid and links itself covalently to the 5’ end

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6
Q

vir region

A

mediates the T region located in the Ti plasmid

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7
Q

T-DNA

A

contains genes that code for enzymes synthesizing opines and phytophormones

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8
Q

Minimal promoter

A

minimal promoter should only have a TATA box and nothing else so it wont work without enhancers or silemcers

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9
Q

Chimeric protein

A

protein made of one subunit from transcription from one source and other subunit from forgein subscript

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10
Q

Nuclear Targeting Signal

A

an amino acid sequence that tags a protein for import into the cell nucleus by nuclear transport

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11
Q

Transcription Factor

A

a protein that controls the rate of transcription of genetic info from dna to mRNA

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12
Q

Auxin

A

promotes elongation

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13
Q

Cytokinin

A

promotes cell division

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14
Q

Size of an average gene

A

8kb

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15
Q

Size of an average enhance

A

between 50 and 1500

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16
Q

list the 3 essential domains of the bacterial tetR protein

A

DNA binding domain
tet binding domain
protein-protein interaction domain

17
Q

Can new domains be added anywhere in a protein without disrupting functions

A

any domain can be put anywhere without losing function but they cannot be inserted into another domain

18
Q

How can we determine whether a particular region of a gene acts as an enhancer or stimulates transcription in some other way? What tests are there?

A

an enhancer can be moved upstream/downstream/inverted/in an intron from a gene and still work BUT CANNOT WORK IN TRANS
so we would take the region we suspect and clone it in those places, transform, and measure gene expression

19
Q

Why would anyone put a bacterial origin into an artifical transposon designed for use in eukaryotes?

A

To make cloning back easy- easier to multiply and manipulate genes in e coli

20
Q

Name 1 specific functional motiff found in most eukaryotic promoters

A

TATAATA box

21
Q

What determines the strength of a promoter

A

How tight the RNA polymerase binds to the TF

22
Q

What is the function of a polyA tail

A

responsible for determining where mRNA will be processed to make it functional

23
Q

T or F: in eukaryotes constitutively expressed genes use a single enhancer that is functional in all cells all the time

A

true - C?GCG?CG motif replaces TATA box and is the constitutively promoter

24
Q

T or F: eukaryotic transcription terminates at defined sequences

A

False- it is unknown exactly what sequence terminates transcription but it is thought the polyA tail has something to do withit

25
Q

What is the nopaline synthase gene

A

Gene responsible for producing the carbon compound nopaline which can only be used by agrobacterium

26
Q

What is the octopine synthase gene

A

in T-DNA ti plasmid expressed in plant host cells

27
Q

what is T-DNA

A

the specific portion of agrobacterium plasmid that is transferred into a plant and encorporated into the genome

28
Q

can an integrated t-dna move again within the plant

A

no it lacks a transposase

29
Q

What is the preferred way of introducing a construct from the test tube to a mouse egg

A

injecting the desired gene into the pronucleus of a fertilized mouse egg

30
Q

in what ways does T DNA transfer resemble plasmid conjugation

A

a pileus is formed and the DNA moves from agro to plant cells like conjugation (both linear forms)