Molecular Tools-II:

Restriction Enzymes.

Restriction enzymes are characterized by -they are restricted to prokaryotic organisms (with certain exceptions); they act on foreign DNA, but not on their own; they act at a particular site or sequence specific; they cut the DNA into fragments in a specific way.

Genome mapping using Restriction enzymes;

http://utcinnovationlabs.blogspot.com/

Restriction enzymes: http://www.symposcium.com/

Most of the restriction enzymes now available are isolated from specific microorganisms. Each of the microbes produces specific enzymes and the name of the RE’s is derived form the name of the organism. Based on the structure and function they are classified into three types, Type I, II and III.

Type-I Enzymes:

Most of them are multimeric enzymes. They undertake both methylation and restriction activities. Type-I enzymes have three groups of related genes. The genes concerned are ‘Host specificity of DNA’ ‘Had’ systems. Strain E.co-K shows three variants of ‘Had’ system. E.co-B shows two variant of ‘Had’.

E.co K enzymes consist of three types of subunits called R, M, and S, exist as complex of 2 R subunits, 2 M subunits and 1 S subunit. The genes for them are hsd-R, hsd-M and hsd-S.

The R subunit is responsible for restriction activity. The M subunits are for methylation and S subunits for recognizing the site; on the contrary E.coli-B consists of only M and S subunits in 1: 1 ratio. In this the S subunit recognizes the site. This is followed either restriction or methylation, which events are mutually exclusive.

E.co-B and E.co-K genes are allelic, their target sequences are different, but in diploid state the S of one strain can direct the activities of R and M to the recognition site

Recognition site of both K and B are bipartite, each consists of specific 3 bp and 4 bp sequences separated by few bp. So the recognition surface of both lie on the same side of the DNA. The possess Adenine residue that can be methylated on the opposite strands.

5’ TGA (N) 8 TGCT

3’ ACT (N) 8 ACGA

Methylation of Adenine is performed by S-Adenosyl Methylase (dAM), Adenosyl carries methyl group.

Methylation of Cytosine is performed by Cytidyl Methylase (dCM).

Whether the target to be cleaved or methylated depends upon the state of the site in the DNA. If the target is fully methylated, the enzyme binds to and gets released without cutting. If the target is hemi methylated the complex binds and methylates the site to fully methylated state and the enzyme is released from the site. If the target is unmethylated the enzyme binds and gets triggered for cleavage activity.

The cleavage is generally 400 to 1000 base pairs away from the binding site. It is believed that when once the enzyme binds it pulls the DNA through second binding site (via loop formation) and recognizes the site for cutting. Then after some time the enzyme gets released from the site.

DNA: 5’ -I-P-I---hsd-R-I-hsd-M-I-hsd-S-I-3’

If there are mutations in hsd system one obtains new phenotypes of bacteria. Ex. Mutation in hsd-M prevents restriction and methylation as well and strains will be r^- and M^-. If the mutation is in hsd-R then the strain will be r^-M^+, where they cannot restrict but can modify. If the mutation in the gene hsd-S the strain is r^-m^-, they neither modify nor cut

Type	Number of subunits, require Mg2^+; Mol.wt	Genes/ Mol.wt	Restriction site	Restriction and methylation	Function
Type-I	Bifunctional, 3 subunits, Mg2^+- yes	R= 135 M= 62 S= 55	Bipartite, asymmetric sequences	Mutually exclusive	R=restriction, M= methylation, S= site recognition; cutting is 1000 bp away from the binding site
Type-II	Restriction and methylase functions are separate. Mg2^+ yes		4-6 and 8 bp, often palindromic	Separate reactions	Cut with in the site or adjacent to it
Type-III	Bifunctional, 2 subunits, Mg2^+ yes		5-7bp, asymmetric sequence	Simultaneous	Recognize a region and cut 25-27 bp away from the site

Image result for Nucleotide modification enzymes

www.nature.com

DNA Methylation Research Methods Figure 1

The reaction of DNA methylation; http://www.labome.com/

Determination of differential methylation with methylation-sensitive and methylation-insensitive restriction enzymes.; http://www.labome.com/

Type -III enzymes:

These enzymes are rare. Some strains of E.coli like P1 and P15 carry plasmids P1 and P15 and they carry genes for the said enzymes. The Hinf plasmids found in Hemophilous influenzeae carries serotypes called R.

Each of theses enzymes carries two types of subunits. The R subunit for restriction (cutting), and MS subunits for site recognition and modification and they perform the function almost simultaneously. Interestingly when the enzyme binds to its site (ATP dependent), methylation and restriction activities of the enzymes compete with one another. Methylation takes place at Adenine at the binding site and cleavage takes place 24-27 bp away from the binding site and produces staggered or sticky tails. However, unmethylated site favors binding and cutting.

The MS subunit has molecular mass of 75 KD and of R is about 108KD.

5’AGACC

3’TCTGG for P1

5’CAGCAG

3’GTCGTC for P15,

AGA*CC-----GGTCT

TCTGG-------CCA*GA requires inverted repeats next to the recognition site.

Unmethylated site facilitate the binding and restriction;

AGACC---GGTCT

TCTGG---CCAGA

Restriction

AGACC GGTCT

TCTGG CCAGA

Type-IV Enzymes:

These are special kind of enzymes, which cut the sites only when they are methylated. They use tetramer or hexamer sites but the A in the site should be methylated.

Ex. Dpn-I from Streptococcus pneumoniae cuts > GATC, only if it is methylated, but the bacteria have no methylase activity. Another strain produces a variety called Dpn-II, which cleaves GATC when it is not methylated, but the strain produces methylase enzyme.

Another enzyme from a phage PI cleaves TGATCA > only when the site is methylated at Adenine. The enzyme is called Pac case.

Type-II Enzymes:

These enzymes are extensively used in recombinant DNA techniques.

Restriction enzymes recognition sequences: http://www.vivo.colostate.edu/

They are the most abundant group of enzymes. Restriction and methylation are exclusively separate reactions. They are made up of homo-dimmers. They recognize a set of sequences, which can be four base pairs or six base pairs; some times rarely the sequence can be 8 or more bases paired. In most of the cases the sequence are palindromic in nature and actually they provide half sites for the enzyme binding and cutting. The enzymes use tetramer, hexamer or octamer sequences and can generate 5’ overhangs, 3’ overhangs or blunt ends, but they are strictly sequence specific. Fully methylated sites are not cut with certain exceptions. Hemi methylated sites are not cut but non-methylated sites are restricted. However, methylase is a monomer, and methylates cytosine to 5-me-cytosine, or 4-me-cytosine or and methylates adenine to6-me-Adenoine

They are grouped as group -I, II, III and IV. Each group contains subgroups. Subgroup A produces 5’ overhangs, subgroup-B which generates 3’ overhangs and sub group-C produces blunt ends. Specific microbes or specific strains of a species synthesize all these enzymes. Such organisms have been genetically manipulated for higher yield. The organisms used for isolating restriction enzymes belong to aerobic, anaerobic, photosynthetic, diazotrophic, mesotropic, thermophilic or psychrophilic and they may be slow growing or fast-growing types. Only few examples have been given.

Group-I:

Sub group-A generates 5’ sticky tails:

(*= Position of cutting)

Name	Sequence
Sau 3A	*GATC
Nde I
Nde II
Taq I	T*CGA
Mbo I
Nar I	GG*CGCC
Xma I	C*CCCGGG
EcoR I	G*AATTC
BamH I	G*GATCC
Bst I	G*GATCC
Bgl II	A*GATCT
Xho I	C*TCGAG
HinD III, Xba I	AAGCTT TCTAGA
Xba IT	8CTAGA
Nco I	C*CATGG
Not I	GC*GGCCGC

Sub group-B produce 3’ sticky tails:

Name	Sequence
Hna I	GCG*C
Sac II	CCGC*GG
Sph I	GCATG*C
Kpn I	GGTAC*C
Sac I	GAGCT*C
Pst I	CTGCA*G

Sub group-C produce blunt ends:

Name	Sequence
Alu I	AG*CT
Hae III	GG*CC
Sma I	CCC*GGG
Eco RV	GAT*ATC
Dra I	TTT*AAA
Hapa I	IGTT*AAC

Group -II: Use interrupted palindromic sequences and generate 5’, or 3’ or blunt ends (few examples).

Sub group-A:

Sub group-B:

Sub group-C:

Few Examples

Name	Sequence
Dcle I	C*TNAG
Sau I	CC*TNAGG
Sfi I	GGCCNNNN*NGGCC
Xmn I	GAANN*NNTTC

Group-III: They use slightly relaxed sequences; they also generate 5’or 3’ or blunt ends (few examples).

Sub group-A:

Sub group-B:

Sub group-C:

Name	Sequence
EcoR II	*CCA/TGG
Xho II	Pu*GATCpy
Hae II	PuGCC*py
Hinc II	Gtpy*puAC

Group IV: They use non-palindromic sequences. They again generate 5’ or 3’ sticky tails or blunt ends (few examples)

Sub group-A:

Sub group-B:

Sub group-C:

Name	Sequence
Fok I	GGGAGGATGN9* CTTCTN7*
Hph I	GGTGAN8* CCACTN7*
Mbo II	GAAGAN8* CTTCTN7*
Mnl I	CCTCN7* GGAGN7*

The most famous RE- is EcoR1; http://www.accessexcellence.org/

E.co R1 enzyme; http://www.austincc.edu/

Rare cutting Enzymes:

Such enzymes are very useful in generating genomic library.

Not I - one in 1000,000 bp

Sfi I - one in 1000 000 bp

Dma I- one in 60 000bp

Sac II - one in 60 000bp

Dra I- one in 20 000 bp

Xba I- one in 5000 bp

Isoschizemers:

They are different enzyme recognize the same sequence and cut differently.

Sma I/ Xma I / Cfrg I CCC*GGG

Msp I / Hapa II C*CGG

SST I / Sac I GAGCT*C

Nde II / Mbo I / sau3A *GATC

Nhe I / Sph I G*CTAGC.

Kpn I / Acc65 I

Mbo I / Sau3A I.

Sma I / Xma I.

Saph I / Bbu I.

Compatible ends:

Enzymes which produce similar sticky tails use the same sequence; they are very helpful in ligating the DNA fragments.

Sal I / Xho I cut with Taq I

Bgl II / BamH I cut with Mbo I

Xba I / Spo I cut with Bra I

Mbo I / BamH I cut with Mbo

Sau3AI / Bgl II cut with Mbo I

Bgl II/ Bcl I/Nde II

Sau3A I / Xho II’

Mbo I/Dpn I, Nde II, Sau3A I,

Dra I/ Aha II

Kpn I/ asp 718,

Pst I/ Nsci I

Sac I/Sst I

Sal I/Xho I,

Enzymes not inhibited by Dam methylation i.e. methylation of A in GATC sequence:

BamH I G/GAT*CC

Bgl II A/GA*TCT

Sau3A I /GA*TC

Xho II puG*TCpy

Enzymes not inhibited by DCM methylation i.e. methylation at C in a GG//CC or CGCG sequences:

BamH I G/GATCC*

Kpn I GGTAC/C*

Nar I GG/CGCC*

Hae III GG/CC*

Sfi I GGCC*N5GGCC*

Dpn I GATC*

Restriction sites that contain ATG sequence:

Such sequences are helpful in cloning DNA in expression mode. Such sequences can be introduced for initiating translation in generating proper reading frame.

Nco I C*CATGG

Nde I CA*TATG

Sph I GCATG*C

Fok I GGATG9*/13*/

Bbn I GCATG*C

Eco T121 ATGC*T

Microbes, their enzymes and their cutting sequence:

Microbe	Enzyme	Sequence
Arthobacter luteus	Alu I	*AGCT**
Bacillus amyloliquefaciens.H	BamH I	*GGATCC**
Bacillus globigii	Bgl I	*GCCNNNNNBGC**
Bacillus globigii	Bgl II	*AGATCT**
Dienococcus radiophilous	Dra I	*TTTAAA**
Escherichia coli R1	E.coli RI	*GAATTC**
E.co RV	E.co RV	*GATATC**
Hemophilous aegypticus	Hae III	*GGCC**
Hemophilous influenzae r. D 3	HinD3	*AAGCTT**
Hemophilous parainfluenzae	Hapa I	*GTTAAC**
Klebsiella pneumoniae	Kpn I	*GGTACC**
Nocordia corallia	Nco I	*CCATGG**
Nocordia otidis cavarium	Not I	*GCGGCCGC**
Providencia stuartis	Pst I	*CTGCAG**
Streptomyces achronogenes	Sac I	*GAGCTC**
Streptococcus aureus 3A	Sau3A	*GATC
Streptococcus caespitsus	SCA I	*AGTACT**
Streptococcus fimbriatus	Sfi I	*GGGCNNNNNGGC**
Serratus marcescens	Sma I	*CCCGGG**
Xanthomonas badrii	Xba I	*TCTAGA**
Xanthomonas malvacearum	Xma I	*CCCGGG**

Application of Restriction Enzymes:

Enzymes have very wide use, especially in biochemistry, molecular biology, biotechnology, agriculture and medicine. They can be used in the following applications.

· Characterization of DNA.

· Size fractionation of genomic DNA.

· Cutting DNA at the required regions.

· Restriction site mapping.

· Can be used for RFLP studies.

· Restriction sites can be used for PCR amplifications using sequence specific primers.

· Can be used in recombinant DNA methods.

· Used in cloning and sub cloning and sequencing.

· Can be used in disease diagnosis.

· Can be used in creating in vitro mutagenesis.

· Many more.

Restriction Site Mapping:

It is a very useful technique, so one can analyze a DNA fragment where one uses it for marking a position; they act as flag post for molecular biologists.

This technique along with end sequencing one can align fragments of DNA in a sequence, which is used for contigs alignment.

RE mapping; http://www.wormbook.org/

Take a piece of DNA from the clone, let us say it is 10kbp long or more label the 5’ends with radioactive 32P. Clean the DNA free of the small 32P piece.

Assume the length of the DNA taken is 10KBp long and cut with E.coli I. Similarly use another piece of the DNA cut it with Bam HI, Another with Pst I. Then separate each of the fragments cut by different enzymes on Agarose gel using different slots. Note, in each of the cuttings only the fragment with label will show up in gel that is dried and auto radio graphed. The other piece though found in the same slot does not show up as radioactive fragment.

For example, the DNA contains the label at one end. When you cut with E. coli R1, it will cut at many site randomly (short period of time), wherever the sequence is found, but among these only one contains the tag. Remember the digestion should be partial and should not be complete. Partial means one enzyme cuts one of the several fragments at one site not more. For this one has to adjust the concentration of the substrate and the enzymes.

*I--1--2--3--4--5--6--7--8--9--I

Here the length is denoted by the number of nucleotide; 1=1000.2=2000 and so on. The astrich shows the position of the label. Let us say E.coli has cut at position 2, 4 and 8. When you run the fragment on an Agarose gel and look for the radioactivity only 3 bands appear i.e. one with 0-2, 0-4 and 0-8, so three fragments are visible and we know where the sites for E.coR1 are present. Similarly cut with Bam H I, let us say it has sites at 3, 5 and 9; you get 3 fragments. Use another enzyme Pst I and let us say it cuts at 1, 6 and 7; this produces 3 fragments.

If such fragments cut by each enzymes are run on different slots, one can read the RE site of each and the size of each fragment and the sequence of each site. One has to use the marker for the size of the size of the fragment.

Marker	E.coR I	Bam H I	Pst I
-------1			-----
-------2	------
-------3		------
-------4	-------
-------5		------
-------6			------
-------7			------
-------8	-------
-------9		------
-------10

Now read the fragments and their site from the bottom. The bottom most fragment is 9, it is Bam H 1, the next fragment is at 8, it is E.coR I, the next is at 7 i.e at Pst1. If you go on reading you get the sequence of RE sites like.

I----Pst I-EcoRI-BamH-RI-BamH1-Pst1-Pst1-R 1-BamH1---I.

Thus, one knows where the site for each of the REs. This greatly help in cloning, sequencing, aligning each fragment in sequencing, creates mutations by deleting and filling up the cut ends, can be used for chromosomal waking.

http://www.siumed.edu/

Chromosome walking; http://www.bio.davidson.edu/