DNA Libraries Flashcards

0
Q

Uses of genomic library

A
  • architecture and structure of genes
  • sequencing of entire genome
  • control of expression
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1
Q

Definition of DNA library

A

A collection of all DNA sequences that represent the genome of an organism/cell, each of which has been cloned into a vector to enable production, isolation, storage and analysis

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2
Q

Uses of cDNA libraries

A
  • sequence of protein coding region
  • production of new or modified protein
  • gene expression: tissue specific and temporal pattern
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3
Q

How big should a genomic library be?

A

Must contain sufficient number of recombinants in order to ensure a high probability of it containing any particular sequence of genome

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4
Q

Process of constructing a genomic library

A
  • purify genomic DNA
  • fragment the DNA (restriction enzymes)
  • clone the fragments into vectors
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5
Q

Why use partial digestion in genomic libraries?

A
  • overlapping sequences allow for ‘chromosome walking’

- can use the end of one insert as a DNA probe to screen the library for adjacent fragments

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6
Q

Methods for having overlapping clone s

A
  • partial digestion with restriction enzyme

- mechanical shearing

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7
Q

How to achieve a partial digestion of genomic DNA

A
  • vary the amount of enzyme
  • increase the time of digestion
  • reduce the temp of digestion
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8
Q

How is partially digested genomic DNA fractionated?

A

By running the digested DNA on a sucrose gradient

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9
Q

Two ways that a lambda phage can carry DNA

A
  • insertion vector (small 7kb)

- replacement vector (large 20kb)

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10
Q

Advantage of using lambda phage

A

Enables infection (a more efficient way of introducing DNA in bacteria)

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11
Q

What are cosmids?

A

Combo of a plasmid and a phage

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12
Q

Methods of screening gnomic libraries

A
  • hybridisation

- colony and plaque hybridisation

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13
Q

How to isolate mRNA

A
  • most mRNAs are polyadenylated at their 3’ends

- oligo dt can be bound to the polyA tail and used to recover the mRNA

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14
Q

How to screen cDNA libraries

A

Use nucleic acid probe to screen the library based on hybridization with nucleic acids

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15
Q

How to screen for cDNA protein product

A
  • use expression vector
  • introduce cDNA in the frame
  • down stream to B-gal
  • will be expressed during the lysogenc cycle of the virus
16
Q

What is RACE used for?

A

To obtain the full-length sequence of an RNA transcript found within a cell

17
Q

How do marathon libraries for PCR based cloning work?

A
  • need knowledge of a short DNA sequence of the gene to be cloned
  • obtain dsDNA and ligase adaptors to the ends
  • these adaptors are complimentary and can perform PCR to synthesise fragment corresponding to desired gene
18
Q

Steps in creating a cDNA library

A
  • mRNA isolation/purification
  • check RNA integrity
  • fracionate and enrich RNA
  • synthesis of cDNA
  • treatment of cDNA
  • ligate to vector
19
Q

What is needed for cDNA creation?

A
  • reverse transcriptase
  • dNTPs
  • primers
20
Q

Characteristics of lambda phage

A
  • dsDNA around 50kb
  • has lytic and lysogenc life cycles
  • central 20kb not required for the lytic cycle
  • replication and packing requires 50kb DNA and 10kb
  • packaging requires recognition sequences 50kb apart
21
Q

Characteristics of a cosmic

A
  • has COS site
  • packages like a phage
  • once in bacteria, acts like a plasmid
22
Q

Definition of screening

A

Process of identifying one particular clone, containing a gene of interest

23
Q

Process of hybridisation

A
  • transfer DNA onto nylon or nitrocellulose gel
  • hybridize with probe
  • remove un hybridized probe
  • visualize (xray)
  • select positive from master plate
24
Q

Definition of hybridisation

A

Using radio labelled probes that are complementary to the gene of interest