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GENE
MANIPULATION
Msc.part2(bioanalyticalsciences)
Paper:1
Roll No.:3
INDEX
 INTRODUCTION.
 HISTORY.
 PROCESS.
 RESTRICTION ENZYMES.
 REFERENCE.
 CONCLUSION.
INTRODUCTION
 Gene manipulation means arrangement of
genes within the organism externally.
 It is also known as genetic engineering.
 Genes are the pieces of DNA and carrier of
the genetic information which determines
the all characteristics of an individual.
HISTORY
 At first the gene manipulation was used in
the agriculture to improve the quality of
plants.
 It was discovered in 2001 in native Mexican
corn.
PROCESS
 1) ISOLATION OF DNA FROM ORGANISM.
 2)INTRODUCTION OF DNA INVECTOR / IN
PLASMID BY USING RE (RESTRICTION
ENZYME)
 3)TRANSFORMATION INTOTHE HOST CELL.
RESTRICTION ENZYMES
 Restriction endonucleases (also called restriction
enzymes) are some of the most Restriction enzymes
recognize specific sequences in DNA and then
cleave
 the phosphodiester bonds between the nucleotides
at that site. Any time
 this sequence appears in DNA it will be cleaved by the
enzyme, whether it is viral
 or frog or human DNA.This is why restriction enzymes
are so critical to
 molecular biology; they are very specific, cutting only
at their unique recognition site.
 Restriction enzymes recognize specific sequences in DNA
and then cleave
 the phosphodiester bonds between the nucleotides at
that site. Any time
 this sequence appears in DNA it will be cleaved by the
enzyme, whether it is viral
Nucleic Acids
Type I enzymes
Enzyme Recognition Me site3 Reference
sequence
EcoAI GAGNNNNNNNGTCA 2(6) -3(6) 545,546
EcoBITGANNNNNNNNTGCT 3(6) -4(6) 547-551
EcoDITTANNNNNNNGTCY 552
EcoDXXITCANNNNNNNATTC 553,554
EcoEI GAGNNNNNNNATGC 555,556
EcoKI AACNNNNNNGTGC 2(6) -3(6) 557-560
EcoRI24/3IGAANNNNNNNRTCG -3(6) 561
EcoR124I GAANNNNNNRTCG 561
StySBI GAGNNNNNNRTAYG 2(6) -4(6) 562
StySJI GAGNNNNNNGTRC 563
StySPIAACNNNNNNGTRC 2(6) -3(6) 562
StySQIAACNNNNNNRTAYG
REFERENCE
 WEBLIOGRAPHY:
 www.sciencedirect.com
 www.pharmatutor.com
 BIBLIOGRAPHY:
 Principles of gene manipulation and genomics
by S. B. Primrose and R.Twyman.
CONCLUSION
 Gene manipulation includes gene splicing .
 Use of recombinant DNA.
 Forming of monoclonal antibody.
 Or we use PCR thermo cycler.
 In humans genetic manipulation is not allowed.

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Gene manipulation

  • 2. INDEX  INTRODUCTION.  HISTORY.  PROCESS.  RESTRICTION ENZYMES.  REFERENCE.  CONCLUSION.
  • 3. INTRODUCTION  Gene manipulation means arrangement of genes within the organism externally.  It is also known as genetic engineering.  Genes are the pieces of DNA and carrier of the genetic information which determines the all characteristics of an individual.
  • 4. HISTORY  At first the gene manipulation was used in the agriculture to improve the quality of plants.  It was discovered in 2001 in native Mexican corn.
  • 5. PROCESS  1) ISOLATION OF DNA FROM ORGANISM.  2)INTRODUCTION OF DNA INVECTOR / IN PLASMID BY USING RE (RESTRICTION ENZYME)  3)TRANSFORMATION INTOTHE HOST CELL.
  • 6. RESTRICTION ENZYMES  Restriction endonucleases (also called restriction enzymes) are some of the most Restriction enzymes recognize specific sequences in DNA and then cleave  the phosphodiester bonds between the nucleotides at that site. Any time  this sequence appears in DNA it will be cleaved by the enzyme, whether it is viral  or frog or human DNA.This is why restriction enzymes are so critical to  molecular biology; they are very specific, cutting only at their unique recognition site.
  • 7.  Restriction enzymes recognize specific sequences in DNA and then cleave  the phosphodiester bonds between the nucleotides at that site. Any time  this sequence appears in DNA it will be cleaved by the enzyme, whether it is viral
  • 8. Nucleic Acids Type I enzymes Enzyme Recognition Me site3 Reference sequence EcoAI GAGNNNNNNNGTCA 2(6) -3(6) 545,546 EcoBITGANNNNNNNNTGCT 3(6) -4(6) 547-551 EcoDITTANNNNNNNGTCY 552 EcoDXXITCANNNNNNNATTC 553,554 EcoEI GAGNNNNNNNATGC 555,556 EcoKI AACNNNNNNGTGC 2(6) -3(6) 557-560 EcoRI24/3IGAANNNNNNNRTCG -3(6) 561 EcoR124I GAANNNNNNRTCG 561 StySBI GAGNNNNNNRTAYG 2(6) -4(6) 562 StySJI GAGNNNNNNGTRC 563 StySPIAACNNNNNNGTRC 2(6) -3(6) 562 StySQIAACNNNNNNRTAYG
  • 9.
  • 10.
  • 11.
  • 12.
  • 13. REFERENCE  WEBLIOGRAPHY:  www.sciencedirect.com  www.pharmatutor.com  BIBLIOGRAPHY:  Principles of gene manipulation and genomics by S. B. Primrose and R.Twyman.
  • 14. CONCLUSION  Gene manipulation includes gene splicing .  Use of recombinant DNA.  Forming of monoclonal antibody.  Or we use PCR thermo cycler.  In humans genetic manipulation is not allowed.