Genetic diversity of grapevine (Vitis vinifera L.) as revealed by ISSR markers
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The main goal of this study was to determine the genetic diversity among 36 grape cultivars grown in Palestine by using ISSR-polymerase chain reaction (PCR) fingerprints. Among the tested primers, 17 produced reasonable amplification products with high intensity and pattern stability. A total of 57 DNA fragments (loci) separated by electrophoresis on agarose gels were detected and they ranged in size, from 150 to 900 bp. Out of these fragments, 55 (88%) were polymorphic and 2 (3.5%) monomorphic. Our results also revealed an average of 3.1 loci per primer. A minimum of 1 and maximum of 10 DNA fragments were obtained (S-17, #820 and #841) and (S-31) primers, respectively. Therefore, the later primer (S-31) is considered to be the most powerful primer among the tested ones. The genetic distance matrix showed an average distance range of between 0.05 and 0.76. The maximum genetic distance value of 0.76 (24% similarity) was exhibited between the (Shami and Marawi.Hamadani.Adi) as well as (Bairuti and Marawi.Hamadani.Adi) genotypes. On the other hand, the lowest genetic distance of 0.05 (95% similarity) was exhibited between (Jandali.Tawel.Mofarad and Jandali. Kurawi.Mlzlz) along with (Shami.Aswad and Shami.mtartash. mlwn) genotypes. Furthermore, the UPGMA dendrogram generally clusters the grape cultivars into eight major clusters in addition to an isolated genotype. Based on these figures, the cultivars tested in this study could be characterized by large divergence at the DNA level. This is taking the assumption that our region has a very rich and varied clonal grape genetic structure.
Abstract
The main goal of this study was to determine the genetic diversity among 36 grape cultivars grown in Palestine by using ISSR-polymerase chain reaction (PCR) fingerprints. Among the tested primers, 17 produced reasonable amplification products with high intensity and pattern stability. A total of 57 DNA fragments (loci) separated by electrophoresis on agarose gels were detected and they ranged in size, from 150 to 900 bp. Out of these fragments, 55 (88%) were polymorphic and 2 (3.5%) monomorphic. Our results also revealed an average of 3.1 loci per primer. A minimum of 1 and maximum of 10 DNA fragments were obtained (S-17, #820 and #841) and (S-31) primers, respectively. Therefore, the later primer (S-31) is considered to be the most powerful primer among the tested ones. The genetic distance matrix showed an average distance range of between 0.05 and 0.76. The maximum genetic distance value of 0.76 (24% similarity) was exhibited between the (Shami and Marawi.Hamadani.Adi) as well as (Bairuti and Marawi.Hamadani.Adi) genotypes. On the other hand, the lowest genetic distance of 0.05 (95% similarity) was exhibited between (Jandali.Tawel.Mofarad and Jandali. Kurawi.Mlzlz) along with (Shami.Aswad and Shami.mtartash. mlwn) genotypes. Furthermore, the UPGMA dendrogram generally clusters the grape cultivars into eight major clusters in addition to an isolated genotype. Based on these figures, the cultivars tested in this study could be characterized by large divergence at the DNA level. This is taking the assumption that our region has a very rich and varied clonal grape genetic structure.
참고문헌 (29)
- Achtak H, "Microsatellite Markers as Reliable Tools for Fig Cultivar Identification", J Amer Soc Hort. Sci, 134(6), pp.624~631 (2009)
- Agarwal M, "Advances in molecular marker techniques and their applications in plant sciences", Plant Cell Reports, 27, pp.617~631 (2008)
- Bahurupe J, "Genetic diversity analysis in chilli (Capsicum annuum L.) using RAPD markers", The international quarterly journal of life sciences, 8(3), pp.915~918 (2013)
- Basheer-Salimia R, "Assessments of Biodiversity Based on Molecular Markers and Morphological Traits among West-Bank, Palestine Fig Genotypes (Ficus carica L.)", American Journal of Plant Sciences, 3(9), pp.1241~1251 (2012)
- Basheer-Salimia R, "Ampelographic and phenotypic characterizations of white Palestinian grapevine cultivars", Palestine Technical University-Kadoorie Research Journal, 3(1), pp.1~11 (2015)
- Basheer-Salimia R, "Identification of Palestinian coloredtable-grape cultivars by means of morphological and pomological descriptors", American Journal of Experimental Agriculture, 9(5), pp.1~15 (2015)
- Basheer-Salimia R, "Climate change and its effects on olive tree physiology in Palestine", Review of Research Journal, 3(7), pp.1~7 (2014)
- Casasoli M, "Genetic linkage map of European chestnut (Castenea sativa Mill.)based on RAPD, ISSR and isozyme markers", Theor Appl Genet, 102, pp.1190~1199 (2001)
- Chittora M, "Molecular markers:An important tool to assess genetic fidelity in tissue culture grown long-term cultures of economically important fruit plants", Asian Journal of Bio Science, 10(1), pp.101~105 (2015)
- Choudhary RS, "ISSR based genotypic differentiation of grape (Vitis vinifera L.)", Bioscan, 9(2), pp.823~828 (2014)
- Depnath S, "Development of ISSR markers for genetic diversity studies in Vaccinium angustifolium", Nordic Journal of Botany, 27, pp.141~148 (2009)
- Dhanorkar VM, "ISSR-PCR for assessment of genetic relationships among grape varieties cultivated in India", Vitis, 44(3), pp.127~131 (2005)
- Herrera R, "Characterization of genetic variation between (Vitis vinifera) cultivars from central Chile using RAPD and inter simple sequence repeat markers", Euphytica, 124, pp.139~145 (2002)
- Jing Z, "Analysis of genetic diversity among Chinese wild Vitis species revealed with SSR and SRAP markers", Genet Mol Res, 12(2), pp.1962~1973 (2013)
- Lima ML, "Analysis of genetic similarity detected by AFLP and coefficient of parentage among genotypes of sugar cane (Saccharum spp.)", Theor Appl Genet, 104(1), pp.8~30 (2002)
- MOA, "Strategy for grape sector in Palestine “2017-2022”" (2017), Publications of the Ministry of Agriculture
- Moreno S, "Inter-simple sequence repeats PCR for characterization of closely related grape vine germplasm", Euphytica, 101, pp.117~125 (1998)
- Qian W, "Genetic variation within and among populations of a wild rice Oryza granulata from China detected by RAPD and ISSR", Theor Appl Genet, 102, pp.440~449 (2001)
- Reddy M, "Inter simple sequence repeat. (ISSR) polymorphism and its application in plant breeding", Euphytica, 128, pp.9~17 (2002)
- Riaz S, "Genetic diversity analysis of cultivated and wild grapevine. (Vitis vinifera L.) accessions around the Mediterranean basin and Central Asia", BMC Plant Biology, 18(137), pp.1~14 (2018)
- Sabir A, "Ampelographic and molecular diversity among grapevine (Vitis spp.) cultivars", Czech Journal of Genetic and Plant Breeding, 45(4), pp.160~168 (2009)
- Santos AR, "An optimized set of microsatellites for grapevine identification", 36th world congress of vine and wine (2013)
- Schluter PM, "Analysis of multi-locus fingerprinting data sets containing missing data", Mol Ecol, 6, pp.569~572 (2006)
- Sripholtaen A, "Application of microsatellite markers for identification of wine grape varieties in Thailand", Asia-Pac J Sci Technol, 21(1), pp.97~110 (2016)
- Sultan S, "Grapevines, establishing, planting, training, pruning, servicing", 459~464 (2005)
- Thomas MR, "Repetitive DNA of grapevine: classes present and sequences suitable for cultivar identification", Theor Appl Genet, 86, pp.73~180 (1993)
- Vignani R, "Microsatellite DNA polymorphism analysis of clones of Vitis vinifera Sangiovese", Sci Hort, 65, pp.163~169 (1996)
- Wang Z, "Survey of plant short tandem DNA repeats", Theor Appl Genet, 88, pp.1~6 (1994)
- Weising K, "Genomic finger printing by microsatellite primed PCR: A critical evaluation", PCR Meth Appl, 4, pp.249~255 (1995)
