The Use of RAPDs Technique for the Detection of Genetic Stability of Date Palm Plantlets Derived From In Vitro Culture of .Inflorescence

The study aimed to use of RAPD - PCR markers to prove the genetic stability of two date palm (Phoenix dactylifera L.) cultivars Barhi and Maktoom produced by tissue culture technique. Inflorescences were excited from adult tree of the two cultivars. Spadixes were divided in to pieces . 0.5 em in len...

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Main Authors: Saleh Bader, Michael Baum, Hussam Khierallah, Wafaa Choumane
Format: Article
Language:Arabic
Published: College of Education for Pure Sciences 2007-10-01
Series:مجلة التربية والعلم
Subjects:
Online Access:https://edusj.mosuljournals.com/article_162828_6416b1bc98789ab9c6641cc065bfb46f.pdf
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author Saleh Bader
Michael Baum
Hussam Khierallah
Wafaa Choumane
author_facet Saleh Bader
Michael Baum
Hussam Khierallah
Wafaa Choumane
author_sort Saleh Bader
collection DOAJ
description The study aimed to use of RAPD - PCR markers to prove the genetic stability of two date palm (Phoenix dactylifera L.) cultivars Barhi and Maktoom produced by tissue culture technique. Inflorescences were excited from adult tree of the two cultivars. Spadixes were divided in to pieces . 0.5 em in length and cultured on MS modified medium<br />supplemented with 100 !lM of 2,4-D and 15 !lM of 2ip. Callus was obtained after 8 weeks and adventitious shoots formation was achieved when callus transferred to MS modified medium supplemented with 10 !lM of 2ip and 5 jlM of NAA. Shoots rooted on half strength MS salts medium supplemented with 5 !lM of NAA with increasing sucrose<br />concentration to 131.5 mM. Plantlets were acclimatized and successfully transferred to soil. RAPD - PCR analysis using 25 universal primers were_performed on DNA extracted from the fresh healthy leaves of the mother tree and from samples randomly taken plantlets derived from tissue culture. Reproducible RAPD patterns were obtained using 20 primers, Seventeen primers showed completely monomorphic bands in all samples tested of the progeny. Only three primers showed some polymorphic bands on the agarose gel for both cultivars in some samples tested comparing with the DNA banding pattern for the intact trees, these were OPD.01 primer for Barhi, and OPB.07 and OPC.08 for Maktom. According to the results above it was obvious that genetic variations could occurred in plantlets derived from callus proliferated from inflorescence of date palm, furthermore RAPD appears to be an efficient technique and a simple fast DNA marker for the early detection of genetic variations in plants propagated by tissue culture technique.
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spelling doaj.art-23a62b48756741c2b655120863edeb512022-12-22T01:21:28ZaraCollege of Education for Pure Sciencesمجلة التربية والعلم1812-125X2664-25302007-10-0120214915910.33899/edusj.2007.162828162828The Use of RAPDs Technique for the Detection of Genetic Stability of Date Palm Plantlets Derived From In Vitro Culture of .InflorescenceSaleh BaderMichael BaumHussam KhierallahWafaa ChoumaneThe study aimed to use of RAPD - PCR markers to prove the genetic stability of two date palm (Phoenix dactylifera L.) cultivars Barhi and Maktoom produced by tissue culture technique. Inflorescences were excited from adult tree of the two cultivars. Spadixes were divided in to pieces . 0.5 em in length and cultured on MS modified medium<br />supplemented with 100 !lM of 2,4-D and 15 !lM of 2ip. Callus was obtained after 8 weeks and adventitious shoots formation was achieved when callus transferred to MS modified medium supplemented with 10 !lM of 2ip and 5 jlM of NAA. Shoots rooted on half strength MS salts medium supplemented with 5 !lM of NAA with increasing sucrose<br />concentration to 131.5 mM. Plantlets were acclimatized and successfully transferred to soil. RAPD - PCR analysis using 25 universal primers were_performed on DNA extracted from the fresh healthy leaves of the mother tree and from samples randomly taken plantlets derived from tissue culture. Reproducible RAPD patterns were obtained using 20 primers, Seventeen primers showed completely monomorphic bands in all samples tested of the progeny. Only three primers showed some polymorphic bands on the agarose gel for both cultivars in some samples tested comparing with the DNA banding pattern for the intact trees, these were OPD.01 primer for Barhi, and OPB.07 and OPC.08 for Maktom. According to the results above it was obvious that genetic variations could occurred in plantlets derived from callus proliferated from inflorescence of date palm, furthermore RAPD appears to be an efficient technique and a simple fast DNA marker for the early detection of genetic variations in plants propagated by tissue culture technique.https://edusj.mosuljournals.com/article_162828_6416b1bc98789ab9c6641cc065bfb46f.pdfrapdsgenetic stabilitydate palm plantlets
spellingShingle Saleh Bader
Michael Baum
Hussam Khierallah
Wafaa Choumane
The Use of RAPDs Technique for the Detection of Genetic Stability of Date Palm Plantlets Derived From In Vitro Culture of .Inflorescence
مجلة التربية والعلم
rapds
genetic stability
date palm plantlets
title The Use of RAPDs Technique for the Detection of Genetic Stability of Date Palm Plantlets Derived From In Vitro Culture of .Inflorescence
title_full The Use of RAPDs Technique for the Detection of Genetic Stability of Date Palm Plantlets Derived From In Vitro Culture of .Inflorescence
title_fullStr The Use of RAPDs Technique for the Detection of Genetic Stability of Date Palm Plantlets Derived From In Vitro Culture of .Inflorescence
title_full_unstemmed The Use of RAPDs Technique for the Detection of Genetic Stability of Date Palm Plantlets Derived From In Vitro Culture of .Inflorescence
title_short The Use of RAPDs Technique for the Detection of Genetic Stability of Date Palm Plantlets Derived From In Vitro Culture of .Inflorescence
title_sort use of rapds technique for the detection of genetic stability of date palm plantlets derived from in vitro culture of inflorescence
topic rapds
genetic stability
date palm plantlets
url https://edusj.mosuljournals.com/article_162828_6416b1bc98789ab9c6641cc065bfb46f.pdf
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