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Inhibition of Leishmania major PTR1 Gene Expression by Antisense in Escherichia coli
Protozoa related to Trypanosome family including Leishmania, synthesize enzymes to escape from drug therapy. One of them is PTR1 that its enzymatic activity is similar to dihydrofolate reductase (DHFR). Dihydrofolate reductase - thymidylate synthase has a major role in DNA synthesis, if it is inhibi...
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Published in: | Iranian journal of public health 2012, Vol.41 (6), p.65-71 |
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creator | Kheirandish, F Bandehpour, M Haghighi, A Mahboudi, F Mohebali, M Kazemi, B |
description | Protozoa related to Trypanosome family including Leishmania, synthesize enzymes to escape from drug therapy. One of them is PTR1 that its enzymatic activity is similar to dihydrofolate reductase (DHFR). Dihydrofolate reductase - thymidylate synthase has a major role in DNA synthesis, if it is inhibited, the result would be the death of parasite. Since PTR1 activity is similar to DHFR, causes the decrease of inhibition effect of drug. The aim of this study was inhibition of Iranian L. major PTR1 expression with mRNA antisense in prokaryotic system as an approach to appear of the drugs therapeutic effects more.
PTR1 gene was ligated to pACYCDuet-1 and pcDNA3 plasmids as sense and antisense plasmids, respectively. Simultaneously transfer of sense and antisense plasmids was done in E. coli strain M15. SDS-PAGE and western blot analysis were carried out to analyze the expression.
Sense and antisense plasmids were prepared and confirmed by restriction analysis and PCR then simultaneously transfer of them was done. SDS-PAGE and western blot analysis showed PTR1 gene was inhibited by mRNA antisense in bacterial cells.
Expression of PTR1 gene in sense plasmid was inhibited successfully by antisense plasmid. |
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PTR1 gene was ligated to pACYCDuet-1 and pcDNA3 plasmids as sense and antisense plasmids, respectively. Simultaneously transfer of sense and antisense plasmids was done in E. coli strain M15. SDS-PAGE and western blot analysis were carried out to analyze the expression.
Sense and antisense plasmids were prepared and confirmed by restriction analysis and PCR then simultaneously transfer of them was done. SDS-PAGE and western blot analysis showed PTR1 gene was inhibited by mRNA antisense in bacterial cells.
Expression of PTR1 gene in sense plasmid was inhibited successfully by antisense plasmid.</description><identifier>ISSN: 2251-6085</identifier><identifier>EISSN: 2251-6093</identifier><identifier>PMID: 23113195</identifier><language>eng</language><publisher>Iran: Tehran University of Medical Sciences</publisher><subject>Enzymes ; Microbiology ; Original ; Parasites ; Parasitic diseases ; Plasmids ; Proteins</subject><ispartof>Iranian journal of public health, 2012, Vol.41 (6), p.65-71</ispartof><rights>Copyright Dr Ali Akbari Sari, Director of The Commission for Accreditation & Improvement of Iranian Medical Journals 2012</rights><rights>Copyright © Iranian Public Health Association & Tehran University of Medical Sciences 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3468993/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3468993/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,4010,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23113195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kheirandish, F</creatorcontrib><creatorcontrib>Bandehpour, M</creatorcontrib><creatorcontrib>Haghighi, A</creatorcontrib><creatorcontrib>Mahboudi, F</creatorcontrib><creatorcontrib>Mohebali, M</creatorcontrib><creatorcontrib>Kazemi, B</creatorcontrib><title>Inhibition of Leishmania major PTR1 Gene Expression by Antisense in Escherichia coli</title><title>Iranian journal of public health</title><addtitle>Iran J Public Health</addtitle><description>Protozoa related to Trypanosome family including Leishmania, synthesize enzymes to escape from drug therapy. One of them is PTR1 that its enzymatic activity is similar to dihydrofolate reductase (DHFR). Dihydrofolate reductase - thymidylate synthase has a major role in DNA synthesis, if it is inhibited, the result would be the death of parasite. Since PTR1 activity is similar to DHFR, causes the decrease of inhibition effect of drug. The aim of this study was inhibition of Iranian L. major PTR1 expression with mRNA antisense in prokaryotic system as an approach to appear of the drugs therapeutic effects more.
PTR1 gene was ligated to pACYCDuet-1 and pcDNA3 plasmids as sense and antisense plasmids, respectively. Simultaneously transfer of sense and antisense plasmids was done in E. coli strain M15. SDS-PAGE and western blot analysis were carried out to analyze the expression.
Sense and antisense plasmids were prepared and confirmed by restriction analysis and PCR then simultaneously transfer of them was done. SDS-PAGE and western blot analysis showed PTR1 gene was inhibited by mRNA antisense in bacterial cells.
Expression of PTR1 gene in sense plasmid was inhibited successfully by antisense plasmid.</description><subject>Enzymes</subject><subject>Microbiology</subject><subject>Original</subject><subject>Parasites</subject><subject>Parasitic diseases</subject><subject>Plasmids</subject><subject>Proteins</subject><issn>2251-6085</issn><issn>2251-6093</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpdkE9LAzEQxRdRbK1-BQl48bKQv5vNRSil1kJBkXoO2XTqpuwmdbMV--2NWIt6mhnebx4z7yQbUipIXmDFTo99KQbZRYwbjHlBhTzPBpQRwogSw2w597WrXO-CR2GNFuBi3RrvDGrNJnToaflM0Aw8oOnHtoMYv8Bqj8a-dxF8BOQ8mkZbQ-dsndZsaNxldrY2TYSrQx1lL_fT5eQhXzzO5pPxIq8Zo31eVGTNV4SXUiqBC2aF4pRTYnFRAYE0WqNMEgQxqihFWSlZSIbVikswGNgou_v23e6qFlYWfN-ZRm8715pur4Nx-q_iXa1fw7tmvCiVYsng9mDQhbcdxF63LlpoGuMh7KImhIqUmGQ8oTf_0E3YdT69pwmmuJSKS5Go698XHU_5CZx9AkOCfDI</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Kheirandish, F</creator><creator>Bandehpour, M</creator><creator>Haghighi, A</creator><creator>Mahboudi, F</creator><creator>Mohebali, M</creator><creator>Kazemi, B</creator><general>Tehran University of Medical Sciences</general><scope>NPM</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PYCSY</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>2012</creationdate><title>Inhibition of Leishmania major PTR1 Gene Expression by Antisense in Escherichia coli</title><author>Kheirandish, F ; Bandehpour, M ; Haghighi, A ; Mahboudi, F ; Mohebali, M ; Kazemi, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h332t-6b1f4d1487795063c5942421c06be1ec59ca9a06351a96858b9767309d47ea0e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Enzymes</topic><topic>Microbiology</topic><topic>Original</topic><topic>Parasites</topic><topic>Parasitic diseases</topic><topic>Plasmids</topic><topic>Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kheirandish, F</creatorcontrib><creatorcontrib>Bandehpour, M</creatorcontrib><creatorcontrib>Haghighi, A</creatorcontrib><creatorcontrib>Mahboudi, F</creatorcontrib><creatorcontrib>Mohebali, M</creatorcontrib><creatorcontrib>Kazemi, B</creatorcontrib><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Environmental Science Collection</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Iranian journal of public health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kheirandish, F</au><au>Bandehpour, M</au><au>Haghighi, A</au><au>Mahboudi, F</au><au>Mohebali, M</au><au>Kazemi, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of Leishmania major PTR1 Gene Expression by Antisense in Escherichia coli</atitle><jtitle>Iranian journal of public health</jtitle><addtitle>Iran J Public Health</addtitle><date>2012</date><risdate>2012</risdate><volume>41</volume><issue>6</issue><spage>65</spage><epage>71</epage><pages>65-71</pages><issn>2251-6085</issn><eissn>2251-6093</eissn><abstract>Protozoa related to Trypanosome family including Leishmania, synthesize enzymes to escape from drug therapy. One of them is PTR1 that its enzymatic activity is similar to dihydrofolate reductase (DHFR). Dihydrofolate reductase - thymidylate synthase has a major role in DNA synthesis, if it is inhibited, the result would be the death of parasite. Since PTR1 activity is similar to DHFR, causes the decrease of inhibition effect of drug. The aim of this study was inhibition of Iranian L. major PTR1 expression with mRNA antisense in prokaryotic system as an approach to appear of the drugs therapeutic effects more.
PTR1 gene was ligated to pACYCDuet-1 and pcDNA3 plasmids as sense and antisense plasmids, respectively. Simultaneously transfer of sense and antisense plasmids was done in E. coli strain M15. SDS-PAGE and western blot analysis were carried out to analyze the expression.
Sense and antisense plasmids were prepared and confirmed by restriction analysis and PCR then simultaneously transfer of them was done. SDS-PAGE and western blot analysis showed PTR1 gene was inhibited by mRNA antisense in bacterial cells.
Expression of PTR1 gene in sense plasmid was inhibited successfully by antisense plasmid.</abstract><cop>Iran</cop><pub>Tehran University of Medical Sciences</pub><pmid>23113195</pmid><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Enzymes Microbiology Original Parasites Parasitic diseases Plasmids Proteins |
title | Inhibition of Leishmania major PTR1 Gene Expression by Antisense in Escherichia coli |
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