Molecular cloning is a fundamental technique in molecular biology used to replicate and manipulate DNA fragments. It involves creating multiple identical copies of a specific DNA sequence, typically a gene, and inserting it into a vector (often a plasmid) for further study or manipulation. Here's a...
Chapter 7 Operon and Chapter 8: Major Shift in Transcription
General Transcription Factors:
RNA Processing II: Capping and Polyadenylation
Alles voor dit studieboek (9)
Geschreven voor
Universidad de Zamboanga
BSMLS
Alle documenten voor dit vak (1)
Verkoper
Volgen
millalawi
Voorbeeld van de inhoud
MOLECULAR CLONING METHODS ● Stewart Linn and Werner Arber discovered restriction ●
endonucleases in E. coli in the late 1960s.
4.1 GENE CLONING ● These enzymes get their name from the fact that they prevent
A. THE ROLE OF RESTRICTION ENDONUCLEASES invasion by foreign DNA, such as viral DNA, by cutting it up. ●
● Thus, they “restrict” the host range of the virus.
B. VECTORS
● Furthermore, they cut at sites within the foreign DNA, rather than
C. IDENTIFYING A SPECIFIC CLONE WITH A SPECIFIC PROBE chewing it away at the ends, so we call them endonucleases ●
D. cDNA CLONING (Greek: endo, meaning within) rather than exonucleases (Greek:
exo, meaning outside).
E. RAPID AMPLIFICATION OF cDNA ENDS.
● Linn and Arber hoped that their enzymes would cut DNA at ●
4.2 THE POLYMERASE CHAIN REACTION specific sites, giving them finely honed molecular knives with which
to slice DNA.
A. STANDARD PCR
● Unfortunately, these particular enzymes did not fulfill that hope.
B. BOX 4.1 JURASSIK PARK: MORE FANTASY? ● However, an enzyme from Haemophilus influenzae strain Rd, ●
C. USING REVERSE TRANSCRIPTASE PCR (RT-PCR) discovered by Hamilton Smith, did show specificity in cutting DNA.
● This enzyme is called HindII (pronounced Hin-dee-two).
D. REAL-TIME PCR
● Restriction enzymes derive the first three letters of their names from
4.3 METHODS OF EXPRESSING CLONED GENES the Latin name of the microorganism that produces them.
● The first letter is the first letter of the genus and the next two letters
A. EXPRESSION VECTORS
are the first two letters of the species
B. OTHER EUKARYOTIC VECTORS ● (hence: Haemophilus influenzae yields Hin).
C. USING THE Ti PLASMID TO TRANSFER GENES TO PLANTS. ● In addition, the strain designation is sometimes included; in this
case, the “d” from Rd is used.
● Finally, if the strain of microorganism produces just one restriction
4.1 GENE CLONING
enzyme, the name ends with the Roman numeral I. If more than
● One product of any cloning experiment is a clone, a group of
one enzyme is produced, the others are numbered II, III, and so on
identical cells or organisms.
● HindII recognizes a specific DNA sequence:
● We know that some plants can be cloned simply by taking cuttings
○ GTPyPuAC
(Greek: klon, meaning twig), and that others can be cloned by
○ CAPuPyTG
growing whole plants from single cells collected from one plant.
● and cuts both DNA strands at the points shown by the arrows.
Even vertebrates can be cloned.
○ Py stands for either of the pyrimidines (T or C), and Pu
● John Gurdon produced clones of identical frogs by transplanting
stands for either purine (A or G).
nuclei from a single frog embryo to many enucleate eggs, and a
● Wherever this sequence occurs, and only when this sequence
sheep named Dolly was cloned in Scotland in 1997 using an
occurs,
enucleate egg and a nucleus from an adult sheep mammary gland.
● HindII will make a cut. Happily for molecular biologists,
● Identical twins constitute a natural clone.
● HindII turned out to be only one of hundreds of restriction
● The usual procedure in a gene cloning experiment is to place a
enzymes, each with its own specific recognition sequence. ●
foreign gene into bacterial cells, separate individual cells, and grow
● Table 4.1 lists the sources and recognition sequences for several
colonies from each of them.
popular restriction enzymes. ●
● All the cells in each colony are identical and will contain the foreign
, ● Note, for example, the complementarity between the ends created ● But what about DNA replication? Doesn’t that create newly ●
by EcoRI (pronounced Eeko R-1 or Echo R-1): replicated DNA strands that are unmethylated, and therefore
○ ↓ vulnerable to cleavage? Figure 4.1 explains how DNA continues to
59---GAATTC---39 ---G39 59AATTC— be protected during replication. ●
39---CTTAAG---59 ---CTTAA59 39G— ● Every time the cellular DNA replicates, one strand of the daughter
↑ duplex will be a newly made strand and will be unmethylated. ●
● Note also that EcoRI produces 4-base overhangs that protrude ● But the other will be a parental strand and therefore be methylated.
from the 59-ends of the fragments. This half-methylation (hemimethylation) is enough to protect the ●
● PstI cuts at the 39-ends of its recognition sequence, so it leaves DNA duplex against cleavage by the great majority of restriction
39-overhangs. endonucleases, so the methylase has time to find the site and
● SmaI cuts in the middle of its sequence, so it produces blunt ends methylate the other strand yielding fully methylated DNA. ●
with no overhangs.
● Restriction enzymes can make staggered cuts because the ●
sequences they recognize usually display twofold symmetry.
● That is, they are identical after rotating them 180 degrees. For
example, imagine inverting the EcoRI recognition sequence just
described:
○ ↓
59---GAATTC---39
39---CTTAAG---59
↑
● You can see it will still look the same after the inversion.
● In a way, these sequences read the same forward and backward.
● Thus, EcoRI cuts between the G and the A in the top strand (on
the left), and between the G and the A in the bottom strand (on the
right), as shown by the vertical arrows.
● Sequences with twofold symmetry are also called palindromes.
● In ordinary language, palindromes are sentences that read the
same forward and backward.
● Examples are Napoleon’s lament: “Able was I ere I saw Elba,” or a
Figure 4.1 Maintaining restriction endonuclease resistance after
wart remedy: “Straw? No, too stupid a fad; I put soot on warts,” or a DNA replication.
statement of preference in Italian food: “Go hang a salami! I’m a
lasagna hog.” ● We begin with an EcoRI site that is methylated (red) on both
● DNA palindromes also read the same forward and backward, but strands.
Fig
you have to be careful to read the same sense (59→39) in both ● After replication, the parental strand of each daughter DNA
directions. duplex remains methylated, but the newly made strand of each
● This means that you read the top strand left to right and the bottom duplex has not been methylated yet. ●
strand right to left. ● The one methylated strand in these hemimethylated DNAs is
● One final question about restriction enzymes: If they can cut up enough to protect both strands against cleavage by EcoRI. ●
Voordelen van het kopen van samenvattingen bij Stuvia op een rij:
√ Verzekerd van kwaliteit door reviews
Stuvia-klanten hebben meer dan 700.000 samenvattingen beoordeeld. Zo weet je zeker dat je de beste documenten koopt!
Snel en makkelijk kopen
Je betaalt supersnel en eenmalig met iDeal, Bancontact of creditcard voor de samenvatting. Zonder lidmaatschap.
Focus op de essentie
Samenvattingen worden geschreven voor en door anderen. Daarom zijn de samenvattingen altijd betrouwbaar en actueel. Zo kom je snel tot de kern!
Veelgestelde vragen
Wat krijg ik als ik dit document koop?
Je krijgt een PDF, die direct beschikbaar is na je aankoop. Het gekochte document is altijd, overal en oneindig toegankelijk via je profiel.
Tevredenheidsgarantie: hoe werkt dat?
Onze tevredenheidsgarantie zorgt ervoor dat je altijd een studiedocument vindt dat goed bij je past. Je vult een formulier in en onze klantenservice regelt de rest.
Van wie koop ik deze samenvatting?
Stuvia is een marktplaats, je koop dit document dus niet van ons, maar van verkoper millalawi. Stuvia faciliteert de betaling aan de verkoper.
Zit ik meteen vast aan een abonnement?
Nee, je koopt alleen deze samenvatting voor €3,66. Je zit daarna nergens aan vast.