Transgenics 2 Flashcards

1
Q

Understanding Conditional KOs?
= 4

A
  1. Cell type specific KOs and developmental-age
    specific KOs can now be generated

2 * Site-specific recombinase technology – eg Cre-Lox.
Uses LoxP target sequences & enzyme Cre (a
recombinase) – derived from bacteriophage P1

3 * Activity of the Cre enzyme can be controlled –
expressed in a specific cell type or be triggered by
a specific external stimulus (chemical signal/heat)

4 * Other similar systems (eg FLP-FRT recombination
system) exist

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2
Q

How to Create a Conditional KO mouse?

A

1 -create a transgenic where the gene of interest is flanked by loxP sites, and another in which
the transgene is Cre driven by a specific promoter.

2 -If Cre is active,
catalyses a recombination event between the loxP sites

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3
Q

The Genetic Engineering of Plants -WHY? = 7

A
  1. Herbicide resistance
  2. Pest resistance
  3. Nutritional & flavour
    improvement
  4. Storage & marketability improvement
  5. Land care & rehabilitation
  6. Biofuels
  7. Basic science
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4
Q

Understanding Agrobacterium & the Ti Plasmid = 4

A

Agrobacterium tumefaciens
1 *soil bacterium

2 *causative agent of crown gall disease

3 *infects many diverse species, especially dicotyledons
(entry = wounds)

4 *contains the Ti (tumour inducing) plasmid

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5
Q

What is the Ti plasmid?

A

Ti plasmid:
*T-DNA (transfer DNA)
*flanked by 25 bp repeats
*encodes genes promoting tumour (gall) and bacterial growth

*vir region
* = encodes genes necessary for transfer of T-DNA

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6
Q

Integration of the Transgene into the Plant Genome

A

In an Agrobacterium cell within an infected plant:
1. *nick in one strand of Ti plasmid at one end of T-DNA

  1. *single-stranded DNA-binding protein (SSBP) binds
  2. *second nick at other end of T-DNA
  3. *replication replaces T-DNA region

5 *T-DNA transferred to plant cell nucleus & integrated into chromosome
*one or more copies of T- DNA inserted
*random insertion
*inherited in a Mendelian fashion

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7
Q

Binary Vector System

A

Separation of T-DNA & vir regions - easier manipulation.

Both plasmids required for transformation

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8
Q

Binary Vector System STEPS

A

A. T-DNA in Hybrid plasmid —-> Hybrid plasmid cut open by RESTRICTION ENZYMES –> Foreign DNA with sticky ends into RECOMBINANT PLASMID

B. RECOMBINANT PLASMID —> transferred into AGROBACTERIUM —> agrobacterium tumefaciens; Modified Ti plasmid containing vir gene but no T-DNA

C. Agrobacterium tumefaciens —> INFECTION of tobacco plants to Agrobacterium —> Transgenic tobacco plant —>
DNA = plant chromosomal; DNA, integrated T-DNA with foreign gene

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9
Q

Ti Plasmid T-DNA PROMOTERS ARE…3

A

1 - constitutive - continual
expression of downstream gene

2 - cell/tissue/organ-type specific - activated only in certain cells, tissues or organs

3 - inducible - activated by
chemical/environmental stimulus, resulting in expression of a downstream gene

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10
Q

Ti Plasmid T-DNA
RB AND LB?

A

RB - right border of T-DNA

LB - left border of T-DNA

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11
Q

Ti Plasmid T-DNA - ANTIBIOTIC RESISTANCE…

A

nptII – neomycin
phosphotransferase II gene,
confers kanamycin resistance
(kanr)

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12
Q

How to do Transgeneics in plants?

A
  1. Plant … discs removed from Tobacco leaf
  2. Leaf discs incubated with genetically engineered AGROBACTERIA for 24hrs
  3. Selection medium only allows plant cells that have acquired DNA from the bacteria to PROLIFERATE
  4. callus, SHOOT-INDUCING MEDIUM
  5. shoot (A) Transfer shoot-to- root inducing medium
  6. grow up rotted seeding
  7. adult plant carrying transgene that was originally present in bacteria.
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13
Q

What is BIOLISTICS?

the transgene dna is …4

A

Method of choice for monocotyledons (majority of important food crops)

Transgene DNA
1 *in T-DNA (e.g. between RB & LB)

2 *precipitated onto tungsten or gold particles (1 2 μm diameter)

3 *“shot” into plant cells

4 *particles enter nucleus, DNA integrated into genome

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14
Q

The Uses of Genetically Engineering Plants
- Functional Genomics

A

Forward Genetics
T-DNA insertion libraries of Arabidopsis thaliana

1 *T-DNA used to disrupt genes through insertional mutagenesis

2 *phenotypic screening for loss- and gain-of-function mutations

3 * eg defective flower, metabolism, defect in nutrient uptake

4 *disrupted genes identified by PCR, sequencing, & database searches

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