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Journal articles on the topic 'DNA fingerprinting of plants'

Author: Grafiati

Published: 4 June 2021

Last updated: 30 July 2024

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1

Larson, S. "Plant Genotyping: The DNA Fingerprinting of Plants." Heredity 88, no. 3 (March 2002): 220. http://dx.doi.org/10.1038/sj.hdy.6800054.

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Cerny, Teresa A., and Terri W. Starman. "Molecular Phylogeny and DNA Amplification Fingerprinting of Petunia." HortScience 30, no. 4 (July 1995): 777F—778. http://dx.doi.org/10.21273/hortsci.30.4.777f.

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Seed of five species of petunia and 10 cultivars of Petunia xhybrida were obtained from several sources and plants were fingerprinted using DNA amplification fingerprinting (DAF). Within some species, variable fingerprints were generated between individual plants from the same seed source and/or different sources. Consistencies were found among DAF profiles by bulking the leaf tissue from 10 different plants, but not five plants. Each of 10 octamer primers used during the study revealed polymorphic loci between the species and cultivars. Among the 201 bands produced, 146 (73%) loci were polymo

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Cerny, Teresa A., and Terri W. Starman. "Molecular Phylogeny and DNA Amplification Fingerprinting of Petunia." HortScience 30, no. 4 (July 1995): 777F—778. http://dx.doi.org/10.21273/hortsci.30.4.777.

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Seed of five species of petunia and 10 cultivars of Petunia xhybrida were obtained from several sources and plants were fingerprinted using DNA amplification fingerprinting (DAF). Within some species, variable fingerprints were generated between individual plants from the same seed source and/or different sources. Consistencies were found among DAF profiles by bulking the leaf tissue from 10 different plants, but not five plants. Each of 10 octamer primers used during the study revealed polymorphic loci between the species and cultivars. Among the 201 bands produced, 146 (73%) loci were polymo

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4

Ahmad, Waqar, Khushi Muhammad, Altaf Hussain, Habib Ahmad, Khalid Kahn, Iqbal Ahmed Qarshi, Kamran Iqbal Shinwari, et al. "DNA Fingerprinting of Essential Commercialized Medicinal Plants from Pakistan." American Journal of Plant Sciences 08, no. 09 (2017): 2119–32. http://dx.doi.org/10.4236/ajps.2017.89142.

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5

Munthali, M., B. V. Ford-Lloyd, and H. J. Newbury. "The random amplification of polymorphic DNA for fingerprinting plants." Genome Research 1, no. 4 (May 1, 1992): 274–76. http://dx.doi.org/10.1101/gr.1.4.274.

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6

Anastassopoulos, Elias. "DNA Fingerprinting in Plants. Principles, Methods, and Applications, Second edition." Economic Botany 60, no. 1 (April 2006): 97. http://dx.doi.org/10.1663/0013-0001(2006)60[97:dfippm]2.0.co;2.

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7

Rice, L. J., G. D. Ascough, J. F. Finnie, and J. Van Staden. "DNA fingerprinting of Plectranthus plants for protection of cultivar registration." South African Journal of Botany 76, no. 2 (April 2010): 401. http://dx.doi.org/10.1016/j.sajb.2010.02.040.

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8

Chiang, Yu-Chung, Chang-Hung Chou, Shong Huang, and Tzen-Yuh Chiang. "Possible consequences of fungal contamination on the RAPD fingerprinting in Miscanthus (Poaceae)." Australian Journal of Botany 51, no. 2 (2003): 197. http://dx.doi.org/10.1071/bt02021.

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Fungal contamination has been frequently reported in higher plants. In Miscanthus species, a wide range of fungal flora has also been recorded previously, including an investigation based on nrITS amplification. In order to understand the effects of the fungal genomes on the random amplified polymorphic DNA (RAPD) fingerprinting, callus specimens were obtained from the tissue culture of shoot apices of Miscanthus. RAPD fingerprinting with 60 oligoprimers was conducted with genomic DNA extracted from leaf tissue collected in the field and from the greenhouse, as well as callus derived from the

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9

Zhang, Donglin, Michael A. Dirr, and Robert A. Price. "Application of DNA Markers to the Identification of Horticultural Plants." HortScience 32, no. 3 (June 1997): 534B—534. http://dx.doi.org/10.21273/hortsci.32.3.534b.

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The correct identification of horticultural taxa becomes more and more important for intellectual property protection and economic reasons. Traditionally, morphological characteristics have been used to differentiate among the horticultural taxa. However, the morphological characteristics may vary with plant age, cultural conditions, and climate. Modern technologies, such as DNA markers, are now employed in the identification of horticultural taxa. Currently, technologies of DNA sequencing (gene sequences) and DNA fingerprinting (RAPD, RFLP, SSR, and AFLP) are available for distinguishing amon

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Rao, R., G. Corrado, M. Bianchi, and A. Di Mauro. "(GATA)4 DNA fingerprinting identifies morphologically characterized 'San Marzano' tomato plants." Plant Breeding 125, no. 2 (April 2006): 173–76. http://dx.doi.org/10.1111/j.1439-0523.2006.01183.x.

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11

Butiuc-Keul, Anca, Holger Budahn, Evelyn Klocke, Dragoș Postolache, Anca Farkas, Frank Dunemann, and Ana Coste. "Analysis of Hypericum accessions by DNA fingerprinting and flow cytometry." Acta botanica Croatica 81, no. 1 (January 3, 2022): 1–11. http://dx.doi.org/10.37427/botcro-2021-026.

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Hypericum perforatum, H. umbellatum, H. maculatum, and H. hircinum accessions originating from botanical gardens across Europe were examined by flow cytometry and molecular markers. 2C DNA content of 17 Hypericum perforatum accessions (Hp) and the H. perforatum cultivar Topaz amounted to between 1.56 pg and 1.62 pg. In four Hp accessions some individual plants were found with a DNA content corresponding to 6Cx (2.34 - 2.39 pg). All plants of accession Hp8 showed a DNA content of 6Cx (2.41 pg). In root tips of Hp plants with an average DNA amount of 1.58 pg, 32 chromosomes were detected, corres

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12

Pancaningtyas, Sulistyani, and Agung Wahyu Susilo. "Analysis of Cocoa Clonal Seedlings Purity Through Deoxyribonucleic Acid (DNA) Barcoding and Random Amplification of Polymorphic DNA (RAPD) Fingerprinting." Pelita Perkebunan (a Coffee and Cocoa Research Journal) 38, no. 1 (April 12, 2022): 20–28. http://dx.doi.org/10.22302/iccri.jur.pelitaperkebunan.v38i1.490.

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The genetic purity of a plant indicates the similarity properties between seedlings in the field and the description of the plant in the database. Identifying plant purity through a morphological approach has several drawbacks, including time efficiency and environmental factors, and the diversity is limited and inconsistent. This condition encourages the development of detection methods using DNA molecular markers. Plant identification through fingerprinting or the use of molecular markers has not been widely carried out on a commercial scale, considering the investment costs for this analysi

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13

Ryskov, A. P., A. G. Jincharadze, M. I. Prosnyak, P. L. Ivanov, and S. A. Limborska. "M13 phage DNA as a universal marker for DNA fingerprinting of animals, plants and microorganisms." FEBS Letters 233, no. 2 (June 20, 1988): 388–92. http://dx.doi.org/10.1016/0014-5793(88)80467-8.

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14

Kaemmer, D., K. Weising, B. Beyermann, T. Borner, J. T. Epplen, and G. Kahlm. "Oligonucleotide fingerprinting of tomato DNA." Plant Breeding 114, no. 1 (February 1995): 12–17. http://dx.doi.org/10.1111/j.1439-0523.1995.tb00751.x.

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15

Zurn, Jason D., Katie A. Carter, Melinda H. Yin, Margaret Worthington, John R. Clark, Chad E. Finn, and Nahla Bassil. "Validating Blackberry Seedling Pedigrees and Developing an Improved Multiplexed Microsatellite Fingerprinting Set." Journal of the American Society for Horticultural Science 143, no. 5 (September 2018): 381–90. http://dx.doi.org/10.21273/jashs04474-18.

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Confirming parentage and clonal identity is an important aspect of breeding and managing germplasm collections of clonally propagated, outcrossing crops, like blackberry (Rubus subgenus Rubus). DNA fingerprinting sets are used to identify off-cross progeny and confirm clonal identity. Previously, a six-simple sequence repeat (6-SSR) fingerprinting set was developed for blackberry using a small number of samples. The usefulness of the 6-SSR fingerprinting set for pedigree confirmation had not been evaluated. Therefore, it was used in this study to validate parentage for 6 and 12 biparental popu

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Shirahata, Tatsuya, Hiroshi Ishikawa, Teruhisa Kudo, Yumiko Takada, Azusa Hoshino, Yui Taga, Yusaku Minakuchi, et al. "Metabolic fingerprinting for discrimination of DNA-authenticated Atractylodes plants using 1H NMR spectroscopy." Journal of Natural Medicines 75, no. 3 (February 11, 2021): 475–88. http://dx.doi.org/10.1007/s11418-020-01471-0.

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17

Boiteux, L. S., M. E. N. Fonseca, and P. W. Simon. "Effects of Plant Tissue and DNA Purification Method on Randomly Amplified Polymorphic DNA-based Genetic Fingerprinting Analysis in Carrot." Journal of the American Society for Horticultural Science 124, no. 1 (January 1999): 32–38. http://dx.doi.org/10.21273/jashs.124.1.32.

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Seven plant genomic DNA purification protocols were evaluated for genetic fingerprinting analysis using six tissues obtained from inbred carrot (Daucus carota L.) lines. Evaluations included 1) DNA yield, 2) DNA purity, 3) DNA cleavage with HindIII, 4) DNA integrity, and 5) DNA suitability for amplification in a random amplified polymorphic DNA (RAPD) system. Significant differences were observed among tissues and purification methods for the total amount of DNA. An extraction method using CTAB buffer + organic solvents gave the best results in DNA yield, purity, and HindIII cleavage when comp

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18

Pooler, Margaret R. "Preservation and DNA Fingerprinting of the Historic Tidal Basin Cherries." Journal of Environmental Horticulture 17, no. 4 (December 1, 1999): 189–92. http://dx.doi.org/10.24266/0738-2898-17.4.189.

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Abstract The historic Japanese flowering cherry trees planted around the Tidal Basin in Washington, DC, were given to the United States in 1912 as a gift from Japan, yet only a small portion of the original trees remain. In cooperation with the National Park Service, the U.S. National Arboretum clonally propagated a portion of these trees. DNA from these and other P. x yedoensis plants obtained from domestic commercial nurseries were compared using RAPD markers. Twenty-one 10-nucleotide primers yielded 80 repeatable bands that were used to assess genetic distances among the accessions. The gen

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Heath, Daniel D., Robert H. Devlin, Thomas J. Hilbish, and George K. Iwama. "Multilocus DNA fingerprints in seven species of salmonids." Canadian Journal of Zoology 73, no. 3 (March 1, 1995): 600–606. http://dx.doi.org/10.1139/z95-069.

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DNA fingerprinting is a molecular biological technique that is widely used for identifying parentage and relatedness in plants and animals. To identify new DNA fingerprinting probes for use with salmonids, Southern blots of genomic DNA from chinook salmon (Oncorhynchus tshawytscha) were hybridized at low stringencies with 12 different oligonucleotides designed from published core sequences of variable number of tendem repeats. Seven of the 12 oligonucleotides produced highly variable fingerprint-like patterns; however, only 3 of these had clear, distinct bands. The estimated heterozygosity for

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20

Barnes, S. E., and M. W. Shaw. "Infection of Commercial Hybrid Primula Seed by Botrytis cinerea and Latent Disease Spread Through the Plants." Phytopathology® 93, no. 5 (May 2003): 573–78. http://dx.doi.org/10.1094/phyto.2003.93.5.573.

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Botrytis cinerea occurred commonly on cultivated Primula ×polyantha seed. The fungus was mostly on the outside of the seed but sometimes was present within the seed. The fungus frequently caused disease at maturity in plants grown from the seed, demonstrated by growing plants in a filtered airflow, isolated from other possible sources of infection. Young, commercially produced P. ×polyantha plants frequently had symptomless B. cinerea infections spread throughout the plants for up to 3 months, with symptoms appearing only at flowering. Single genetic individuals of B. cinerea, as determined by

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21

Lamboy, Warren F., Christopher A. Alpha, and David V. Peterson. "Unknown Cultivars of Cold-hardy Grape Can Be Successfully Identified by Their Simples Sequence Repeat (SSR) Fingerprints." HortScience 33, no. 3 (June 1998): 516d—517. http://dx.doi.org/10.21273/hortsci.33.3.516d.

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Simple sequence repeat DNA fragments (SSRs) have been suggested as the method of choice for DNA fingerprinting of grape cultivars. Nevertheless, the use of SSRs as a practical fingerprinting method is not without its pitfalls. For example, when the polymerase chain reaction is used to amplify SSR sequences, potentially confusing “stutter” bands may occur, or there may be non-template directed addition of an “A” to the end of synthesized fragments, or other artifactual amplification products may be produced. Since we would like to fingerprint our entire cold-hardy grape collection of ≈1300 cult

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22

Shufran, Kevin A., William C. Black, and David C. Margolies. "DNA fingerprinting to study spatial and temporal distributions of an aphid, Schizaphis graminum (Homoptera: Aphididae)." Bulletin of Entomological Research 81, no. 3 (September 1991): 303–13. http://dx.doi.org/10.1017/s0007485300033587.

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AbstractThe length of the intergenic spacer in the rRNA cistron varied within and among individuals of Schizaphis graminum (Rondani). Spacer lengths did not vary among offspring of a single maternal lineage (clone). The intergenic spacer was used as a molecular fingerprinting probe on individual aphids and to study spatial and temporal distributions of clones. A spatially nested sampling design was used in wheat and sorghum to estimate numbers of clones among aphids on leaves, among leaves on plants, among plants in fields, among fields in counties, among counties, and among dates. Each level

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23

Hamann, Andrea, Dorothea Zink, and Walter Nagl. "Microsatellite fingerprinting in the genus Phaseolus." Genome 38, no. 3 (June 1, 1995): 507–15. http://dx.doi.org/10.1139/g95-066.

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The genetic variability of the genus Phaseolus was investigated by nonradioactive DNA fingerprinting. The simple repetitive sequences (GATA)4, (GACA)4, (CAC)5, and (CA)8 were used as probes to differentiate 18 species comprised of 90 genotypes. (GATA)4, (CAC)5, and (CA)8 could be detected in the genome of nearly all species, while the (GACA)4 motif occurred only in 13 species. Almost all fragments that hybridized with (GACA)4 also hybridized with (GATA)4. All but two cultivars of Phaseolus vulgaris, P. lunatus, P. acutifolius, and P. polyanthus showed specific banding patterns with (GATA)4. Th

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Park, Dong-Suk, Hee-Wan Kang, Mi-Hee Lee, Young-Jin Park, Byoung-Moo Lee, Jang-Ho Hahn, and Seung-Joo Go. "DNA Fingerprinting Analysis of the GenusPhytophthorain Korea." Mycobiology 31, no. 4 (2003): 235. http://dx.doi.org/10.4489/myco.2003.31.4.235.

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Pradhan, A., G. Yan, and J. A. Plummer. "Development of DNA fingerprinting keys for the identification of radish cultivars." Australian Journal of Experimental Agriculture 44, no. 1 (2004): 95. http://dx.doi.org/10.1071/ea03031.

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Identification of cultivars is extremely important both for cultivation and breeding of crop plants. Cultivar identification based on morphological characteristics can be difficult and complicated. Polymerase chain reaction technologies, such as random amplified polymorphic DNA (RAPD) analysis, can readily and quickly identify cultivars using seeds and young leaves. Sixty individuals representing 7 radish cultivars were examined for RAPD marker polymorphism. Based on the polymorphism generated, 5 primers were selected, out of the 14��examined, to fingerprint the cultivars. The 5 primers produc

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Milic, Dubravka, Jadranka Lukovic, Mihajla Djan, Lana Zoric, Dragana Obreht, Sanja Veselic, G. Anackov, and Theodora Petanidou. "Identification of Salicornia population: Anatomical characterization and RAPD fingerprinting." Archives of Biological Sciences 63, no. 4 (2011): 1087–98. http://dx.doi.org/10.2298/abs1104087m.

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Anatomical and Random Amplified Polymorphic DNA (RAPD) analysis of two typical populations of Salicornia europaea from Montenegro and Greece (Lesvos), one typical population of S. ramosissima from Spain and one population that belongs to the Salicornia genus from Serbia, was undertaken to develop a new strategy for identifying Salicornia plants. Anatomical variability and differentiation were examined using Principal Component Analysis (PCA) and Multivariate Discriminant Function Analysis (MDA). On the basis of the anatomical measurements, the four populations were classified into three groups

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Punitha, D., and T. S. Raveendran. "DNA fingerprinting studies in coloured cotton genotypes." Plant Breeding 123, no. 1 (February 2004): 101–3. http://dx.doi.org/10.1046/j.0179-9541.2003.00921.x.

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Sedláček, Ivo, Pavla Holochová, Ivana Mašlaňová, Marcel Kosina, Cathrin Spröer, Hana Bryndová, Peter Vandamme, Ivo Rudolf, Zdenek Hubálek, and Pavel Švec. "Enterococcus ureilyticus sp. nov. and Enterococcus rotai sp. nov., two urease-producing enterococci from the environment." International Journal of Systematic and Evolutionary Microbiology 63, Pt_2 (February 1, 2013): 502–10. http://dx.doi.org/10.1099/ijs.0.041152-0.

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A set of 25 urease-producing, yellow-pigmented enterococci was isolated from environmental sources. Phenotypic classification divided the isolates into two phena. Both phena were characterized using 16S rRNA gene sequence analysis, DNA base composition, rep-PCR fingerprinting and automated ribotyping. The obtained data distinguished the isolates from all members of the genus Enterococcus with validly published names and placed them in the Enterococcus faecalis species group. DNA–DNA hybridization experiments, pheS and rpoA sequencing and whole-cell protein electrophoresis provided conclusive e

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29

Antonius, Kristiina, Gun Werlemark, and Hilde Nybom. "DNA fingerprinting demonstrates extremely low levels of genetic variation among blackberry cultivars grown in Finland." Agricultural and Food Science 6, no. 3 (September 1, 1997): 241–45. http://dx.doi.org/10.23986/afsci.72787.

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Most blackberry plants cultivated in Finland closely resemble the American species Rubus allegheniensis. Thirty nine such blackberry accessions in the University of Helsinki clone collection were studied by hybridization-based DNA fingerprinting and compared with some known cultivars of R. allegheniensis derivation. ‘lmperial’ appears to be identical to the old cultivar ‘Majestät’, but ‘Earliest of All’ differs considerably. In addition, 37 of the accessions analysed also have DNA fingerprints that appear to be completely identical to that of ‘Majestät’! The remaining two accessions, although

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Gagliardi, Rachel Fatima, Georgia Pereira Pacheco, Carlos Alberto Oliveira, Leonardo Alves Carneiro, José Francisco Montenegro Valls, Maria Lucia Carneiro Vieira, and Elisabeth Mansur. "Rescue of a non-viable accession and rapd analysis of recovered plants of Arachis retusa." Pesquisa Agropecuária Brasileira 39, no. 2 (February 2004): 197–99. http://dx.doi.org/10.1590/s0100-204x2004000200015.

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In vitro regeneration of Arachis retusa was examined for the purpose of germplasm renewal and conservation. Random amplified polymorphic DNA (RAPD) fingerprinting was used to evaluate the genetic stability of plants derived from embryo axes and apical segments. Ten arbitrary decamer primers were screened and five of them were selected. Ninety genomic regions were evaluated, with an average of 18 loci per clone. All amplified segments were monomorphic. The results indicate that recovered plants are genetically stable at the assessed genomic regions and that both regeneration processes are suita

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Byrne, Margaret. "A molecular journey in conservation genetics." Pacific Conservation Biology 24, no. 3 (2018): 235. http://dx.doi.org/10.1071/pc18025.

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Genetics, and more recently genomics, has become an integral part of conservation science. From the early days of DNA fingerprinting through development of hybridisation based and polymerase chain reaction based markers, to applications of genomics, genetics has provided many insights to improve management of plants, animals and their ecosystems. I share my journey of discovery in genetics and genomics, and their application in conservation of plants through understanding evolutionary history, population genetics of rare and threatened species, molecular taxonomy, fragmentation and the role of

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32

Starman, Terri Woods, and Shane Abbitt. "DNA Amplification Fingerprinting Used to Distinguish Series of Cutting, Seedling, and Ivy Leaf Geranium." HortScience 31, no. 4 (August 1996): 565c—565. http://dx.doi.org/10.21273/hortsci.31.4.565c.

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The objective was to distinguish between series of cultivars of Pelargonium xhortorum (zonal geranium), Pelargonium hybrids (seed geranium), and Pelargonium peltatum (ivy leaf geranium) using DNA amplification fingerprinting (DAF) demonstrating the utility of DAF for patent protection to prevent infringement of inventor's rights. Leaf tissue of 10 plants of each cultivar of seedling geranium was bulked for DNA extraction, and cutting and ivy geranium cultivars were bulks of five plants of each cultivar. Isolated DNA from different cultivars of a series were bulked together in their respective

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33

Yashitola, J., A. P. K. Reddy, and Ramesh V. Sonti. "A Widely Distributed Lineage of Xanthomonas oryzae pv. oryzae in India May Have Come from Native Wild Rice." Plant Disease 84, no. 4 (April 2000): 465–69. http://dx.doi.org/10.1094/pdis.2000.84.4.465.

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Xanthomonas oryzae pv. oryzae causes bacterial leaf blight, a serious disease of rice. We have collected leaf blight-affected samples from wild rice (Oryza nivara) plants growing naturally at 22 locations in five revenue districts (Nalgonda, Ranga Reddy, Medak, Nizamabad, and Adilabad) in the Telangana Region of Andhra Pradesh, India. Pathotype analysis on a set of differential rice cultivars and DNA fingerprinting with two multilocus restriction fragment length polymorphism probes indicated that the X. oryzae pv. oryzae strains from the O. nivara plants belonged to a pathotype and lineage pre

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Bittencourt-Oliveira, Mariado Carmo, Ariadnedo Nascimento Moura, Selma Gouvêa-Barros, and Ernani Pinto. "HIP1 DNA fingerprinting in Microcystis panniformis (Chroococcales, Cyanobacteria)." Phycologia 46, no. 1 (January 2, 2007): 3–9. http://dx.doi.org/10.2216/06-01.1.

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Caetano-Anollés, Gustavo, Brant J. Bassam, and Peter M. Gresshoff. "DNA amplification fingerprinting: A strategy for genome analysis." Plant Molecular Biology Reporter 9, no. 4 (November 1991): 294–307. http://dx.doi.org/10.1007/bf02672006.

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Pruvot-Woehl, Solène, Sarada Krishnan, William Solano, Tim Schilling, Lucile Toniutti, Benoit Bertrand, and Christophe Montagnon. "Authentication of Coffea arabica Varieties through DNA Fingerprinting and its Significance for the Coffee Sector." Journal of AOAC INTERNATIONAL 103, no. 2 (March 2020): 325–34. http://dx.doi.org/10.1093/jaocint/qsz003.

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Abstract Background Locating the optimal varieties for coffee cultivation is increasingly considered a key condition for sustainable production and marketing. Variety performance varies when it comes to susceptibility to coffee leaf rust and other diseases, adaptation to climate change and high cup quality for specialty markets. But because of poor organization and the lack of a professional coffee seed sector, most existing coffee farms (and even seed lots and nurseries) do not know which varieties they are using. DNA fingerprinting of coffee planting material will contribute to professionali

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Mia, Md Mukul, Shamsun Nahar Begum, Mirza Mofazzal Islam, M. Sifate Rabbana Khanom, Manas Kanti Saha, Kartik Chandra Saha, and Lutful Hassan. "DNA fingerprinting and chemical analysis of rice genotypes for iron content." Asian-Australasian Journal of Bioscience and Biotechnology 1, no. 1 (April 30, 2016): 1–14. http://dx.doi.org/10.3329/aajbb.v1i1.61524.

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Iron deficiency causes anemia in human body. So identification of iron rich rice genotypes as well as biofortification of staple food crops is an effective way to overcome such malnutrition problems. A total of 46 local rice landraces of Bangladesh were used in chemical analysis and DNA fingerprinting to study their ability to synthesize and accumulate iron content in the grain. Rice plants were grown and their grains were collected and digested by acidKNO3:HClO4. iron concentrations were measured from The highest iron content was found Kumra Ghor (168.52ppm) and the lowest in Patnai Balam (0.

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Pappalardo, L., M. K. Smith, S. D. Hamill, A. M. Stirling, and D. McKay. "DNA amplification fingerprinting analysis of genetic variation withinFusarium oxysporumf.sp.zingiberi." Australasian Plant Pathology 38, no. 1 (2009): 51. http://dx.doi.org/10.1071/ap08076.

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39

Nybom, Hilde. "DNA fingerprinting — A useful tool in fruit breeding." Euphytica 77, no. 1-2 (February 1994): 59–64. http://dx.doi.org/10.1007/bf02551462.

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40

Ilnitskaya, E. T., M. V. Makarkina, R. E. Kazahmedov, E. A. Kozhevnikov, and T. D. Kozina. "A study of genetic profiles of grape plants preserved under the name of Dagestan variety ‘Khatmi’." Plant Biotechnology and Breeding 6, no. 1 (August 26, 2023): 6–12. http://dx.doi.org/10.30901/2658-6266-2023-1-o3.

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Background. Traditionally, the description of grape varieties is a task of ampelographic studies. However, several different grape cultivars have similar phenotypic traits. Molecular genetic characterization is the most accurate tool for cultivar identification. The development of DNA fingerprinting of varieties is the first step in this direction. An extensive database of DNA profiles of grape genotypes makes it possible to determine the varietal affiliation of unknown forms, confirm or refute the varietal correspondence of planting material. ‘Khatmi’ is an autochthonous grape variety from Da

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Eskew, D. L., G. Caetano-Anoll�s, B. J. Bassam, and P. M. Gresshoff. "DNA amplification fingerprinting of the Azolla-Anabaena symbiosis." Plant Molecular Biology 21, no. 2 (January 1993): 363–73. http://dx.doi.org/10.1007/bf00019951.

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42

Dabhi M. R., Raghunandan B. L., Patel N. B., Rukhsar, and Patel, S. R. "Report on the Occurrence of Cicada, Platypleura octoguttata (Hemiptera: Cicadidae) on Eucalyptus in Gujarat." International Journal of Environment and Climate Change 13, no. 10 (September 27, 2023): 4157–60. http://dx.doi.org/10.9734/ijecc/2023/v13i103091.

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In order to determine the cicadas spotted on the Eucalyptus plants grown nearby to the college, Anand Agricultural University, Jabugam, between April and June 2022, an investigation was conducted. Adults were brought to the Department of Entomology lab at the College of Agriculture, Anand Agricultural University, Jabugam, for identification in addition to do further research. It is confirmed that the pest is cicadas on the Eucalyptus plant that have been reported from Gujarat, India, based on the morphological traits of the adults and DNA fingerprinting.

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Fiore, Maria Carola, Annalisa Marchese, Antonio Mauceri, Ignazio Digangi, and Anna Scialabba. "Diversity Assessment and DNA-Based Fingerprinting of Sicilian Hazelnut (Corylus avellana L.) Germplasm." Plants 11, no. 5 (February 25, 2022): 631. http://dx.doi.org/10.3390/plants11050631.

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The characterization of plant genetic resources is a precondition for genetic improvement and germplasm management. The increasing use of molecular markers for DNA-based genotype signature is crucial for variety identification and traceability in the food supply chain. We collected 75 Sicilian hazelnut accessions from private and public field collections, including widely grown varieties from the Nebrodi Mountains in north east Sicily (Italy). The germplasm was fingerprinted through nine standardized microsatellites (SSR) for hazelnut identification to evaluate the genetic diversity of the col

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Oppermann, Birgit, Petr Karlovsky, and Werner Reisser. "M13 DNA fingerprinting in unicellular and filamentous green algae." European Journal of Phycology 32, no. 2 (May 1997): 103–10. http://dx.doi.org/10.1080/09670269710001737019.

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Williams, Mark L., Andrew N. Drinnan, and Neville G. Walsh. "Variation within Prostanthera spinosa (Lamiaceae): evidence from morphological and molecular studies." Australian Systematic Botany 19, no. 5 (2006): 467. http://dx.doi.org/10.1071/sb05032.

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Specimens of Prostanthera spinosa F. Muell. representing the geographic range of the taxon were examined for morphological and genetic variation within the species. Patterns of morphological variation were documented and the amplified fragment length polymorphism (AFLP) DNA fingerprinting technique was used to assess the genetic relationships among plants from different populations. Morphological and molecular results were in broad agreement and supported distinct groups in both analyses. The differences detected warrant taxonomic recognition and three species are described representing geogra

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Koohdar, Fahimeh, Neda Aram, and Masoud Sheidai. "Biosystematics, fingerprinting and DNA barcoding study of the genus Lallemantia based on SCoT and REMAP markers." Caryologia 74, no. 4 (March 8, 2022): 77–83. http://dx.doi.org/10.36253/caryologia-1163.

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Lallemantia is a medicinally important plant in the world. Due to interspecific hybridization and horizontal gene transfer, spices relationship and delimitation on the genus Lallemantia is difficult based on different molecular markers. Therefore, selecting the appropriate marker can be important. Fingerprinting techniques continue to be used for genomic profiling for the characterization of germplasm and the establishment of the identity of varieties/hybrids/parental sources of aromatic and medicinal plants. For this, we need to produce detailed information on genetic diversity available in L

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Louws, F. J., J. Bell, C. M. Medina-Mora, C. D. Smart, D. Opgenorth, C. A. Ishimaru, M. K. Hausbeck, F. J. de Bruijn, and D. W. Fulbright. "rep-PCR-Mediated Genomic Fingerprinting: A Rapid and Effective Method to Identify Clavibacter michiganensis." Phytopathology® 88, no. 8 (August 1998): 862–68. http://dx.doi.org/10.1094/phyto.1998.88.8.862.

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The genomic DNA fingerprinting technique known as repetitive-sequence-based polymerase chain reaction (rep-PCR) was evaluated as a tool to differentiate subspecies of Clavibacter michiganensis, with special emphasis on C. michiganensis subsp. michiganensis, the pathogen responsible for bacterial canker of tomato. DNA primers (REP, ERIC, and BOX), corresponding to conserved repetitive element motifs in the genomes of diverse bacterial species, were used to generate genomic fingerprints of C. michiganensis subsp. michiganensis, C. michiganensis subsp. sepedonicus, C. michiganensis subsp. nebrask

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Khlestkina, Elena K., Marion S. Röder, Heinrich Grausgruber, and Andreas Börner. "A DNA fingerprinting-based taxonomic allocation of Kamut wheat." Plant Genetic Resources 4, no. 3 (December 2006): 172–80. http://dx.doi.org/10.1079/pgr2006120.

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AbstractKamut wheat, said to have been derived from seed found in the Egyptian pyramids, appeared on the market about 25 years ago. We have investigated its taxonomic placement using microsatellite genotyping. In all, 89 accessions of 13 tetraploid wheat species, along with samples of Kamut wheat, were genotyped using two A and B genome wheat microsatellite markers per chromosome, generating 453 alleles (8–33 alleles per locus), and a mean allelic polymorphic information content (PIC) of 0.80. A diversity analysis showed that nine major accession groups could be defined, and these were inconsi

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Thimmappaiah, D. Shobha, GS Mohana, J. Dinakara Adiga, and PG Bhat. "Fingerprinting of released varieties of cashew based on DNA markers." Vegetos- An International Journal of Plant Research 29, no. 4 (2016): 89. http://dx.doi.org/10.5958/2229-4473.2016.00105.1.

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Dey, T., and P. D. Ghosh. "Application of molecular markers in plant genome study." NBU Journal of Plant Sciences 4, no. 1 (2010): 1–9. http://dx.doi.org/10.55734/nbujps.2010.v04i01.001.

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The development of molecular techniques for genetic analysis has led to a great increase in our knowledge of plant genetics and our understanding of the structure and behaviour of plant genome. During last three decades, several powerful DNA based marker technologies have been developed for the assessment of genetic diversities and molecular marker assisted breeding technology. In plant systems, the prospects of DNA profiling and fingerprinting is becoming indispensable in the context of establishment of molecular phylogeny, assessment of somaclonal variants, characterization of plant genomics

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