Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene

Objective: Replacment of CD133+ cell’s β globin gene by using a gene targeting constructcontaining the β globin gene and essential elements for homologous recombination.Materials and Methods: pFBGGT was amplified, then digested using the NheI and XhoIrestriction enzymes, and finally, a 13.3 kb band...

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Main Authors: Sirous Zeinali, Bahman Zainali, Mohamadali Shokrgozar, Hossein Khanahmad, Seyedeh Soghra Moosavi, Esmat Kamali, Masood Soleimani, Mojhgan Shaikhpoor
Format: Article
Language:English
Published: Royan Institute (ACECR), Tehran 2010-01-01
Series:Cell Journal
Subjects:
Online Access:http://celljournal.org/library/upload/article/SheikhPoor.pdf
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spelling doaj-908a8073e8184527930df9c055497bc72020-11-25T00:47:46ZengRoyan Institute (ACECR), TehranCell Journal2228-58062228-58142010-01-01122199206Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene Sirous ZeinaliBahman ZainaliMohamadali ShokrgozarHossein KhanahmadSeyedeh Soghra MoosaviEsmat KamaliMasood SoleimaniMojhgan ShaikhpoorObjective: Replacment of CD133+ cell’s β globin gene by using a gene targeting constructcontaining the β globin gene and essential elements for homologous recombination.Materials and Methods: pFBGGT was amplified, then digested using the NheI and XhoIrestriction enzymes, and finally, a 13.3 kb band (naked DNA) was extracted from theagarose gel. Biological activity of positive and negative selection markers were checkedby transfection of COS-7 cells with linear plasmid. Hematopoietic stem cells (HSCs) wereseparated and transfected with linear plasmids using lipofection followed by positive andnegative selection. Polymerase chain reaction (PCR) were done on DNA from the selectedcells and the products were sequenced.Results: The results of biological activity assays showed that selection markers wereactive. PCRs for hygromycin, neomycin and joining segments were positive but PCRs forTK1 and TK2 genes were negative. Sequencing PCR product joining segment confirmedthe formation of homologous recombination.Conclusion: In this novel strategy gene replacement was achieved and biological activitiesof its components were observed.http://celljournal.org/library/upload/article/SheikhPoor.pdfBeta ThalassemiaGene TargetingHomologous RecombinationGene Therapy
collection DOAJ
language English
format Article
sources DOAJ
author Sirous Zeinali
Bahman Zainali
Mohamadali Shokrgozar
Hossein Khanahmad
Seyedeh Soghra Moosavi
Esmat Kamali
Masood Soleimani
Mojhgan Shaikhpoor
spellingShingle Sirous Zeinali
Bahman Zainali
Mohamadali Shokrgozar
Hossein Khanahmad
Seyedeh Soghra Moosavi
Esmat Kamali
Masood Soleimani
Mojhgan Shaikhpoor
Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene
Cell Journal
Beta Thalassemia
Gene Targeting
Homologous Recombination
Gene Therapy
author_facet Sirous Zeinali
Bahman Zainali
Mohamadali Shokrgozar
Hossein Khanahmad
Seyedeh Soghra Moosavi
Esmat Kamali
Masood Soleimani
Mojhgan Shaikhpoor
author_sort Sirous Zeinali
title Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene
title_short Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene
title_full Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene
title_fullStr Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene
title_full_unstemmed Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene
title_sort transfection of human hematopoietic stem cells by a gene targeting construct containing the β-globin gene
publisher Royan Institute (ACECR), Tehran
series Cell Journal
issn 2228-5806
2228-5814
publishDate 2010-01-01
description Objective: Replacment of CD133+ cell’s β globin gene by using a gene targeting constructcontaining the β globin gene and essential elements for homologous recombination.Materials and Methods: pFBGGT was amplified, then digested using the NheI and XhoIrestriction enzymes, and finally, a 13.3 kb band (naked DNA) was extracted from theagarose gel. Biological activity of positive and negative selection markers were checkedby transfection of COS-7 cells with linear plasmid. Hematopoietic stem cells (HSCs) wereseparated and transfected with linear plasmids using lipofection followed by positive andnegative selection. Polymerase chain reaction (PCR) were done on DNA from the selectedcells and the products were sequenced.Results: The results of biological activity assays showed that selection markers wereactive. PCRs for hygromycin, neomycin and joining segments were positive but PCRs forTK1 and TK2 genes were negative. Sequencing PCR product joining segment confirmedthe formation of homologous recombination.Conclusion: In this novel strategy gene replacement was achieved and biological activitiesof its components were observed.
topic Beta Thalassemia
Gene Targeting
Homologous Recombination
Gene Therapy
url http://celljournal.org/library/upload/article/SheikhPoor.pdf
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