Cited by 2Plant tissue culture and regenerationGenetic diversity and population structureGenetic Mapping and Diversity in Plants and Animals

Analysis of diversity using simple sequence repeat (SSR): Distinctions between original Parmentiera cereifera tree and somaclones

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Elshafei, Adel Ahmed, Esmaiel, Naglaa Mohamed·2018·Bulletin of the National Research Centre

Abstract

The possibility of culturing Parmentiera cereifera in vitro was tested. Shoot tips and lateral buds were cultured in three media that were based on Murashige and Skoog (MS) but supplemented with different types and concentrations of growth regulators. Thirty-eight simple sequence repeat (SSR) primers were used to assess the genetic stability of the regenerated plantlets. Lateral buds recorded the highest significant mean values for shoot, root length, and the number of leaves when cultured in MS + 1.2 mg/l of 6-benzylaminopurine (BAP) + 1.5 g/l of activated charcoal. Seeds were also grown in different media. The best results were obtained with MS basal medium. The resulting shoots were rooted in MS medium, with 1.5 g/l of activated charcoal. Regenerated plants were acclimatized in the greenhouse. The 38 SSR primers produced 63 scorable bands ranging from 1 to 3, with an average of 1.68 per primer. Fifty-five monomorphic bands were obtained that ranged from 0 to 3, with an average of 1.45 per primer. The coefficient of similarity matrix ranged from 0.92 to 1.0, with an average of 97.4. Dendrogram generated using the SSR data tended to group the in vitro plants with the mother plant into two major clusters. The first cluster contained 19 in vitro plants with the mother plant and consisted of 4 subgroups. The second cluster contained in vitro plants, P-15, which had the lowest genetic similarity (92%) with the mother plant. The results revealed the increase in the degree of similarity between the tested plants in the SSR analyses. Therefore, micropropagation is a safe mode for multiplication of true-to-type plants of P . cereifera .

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Crossref · 10.1186/s42269-018-0037-y

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  • SSR markers are considered genetically stable because, when used, they did not reveal any polymorphism, or only a very low level of it, between the original plants and the regenerants.

    “SSR markers are considered genetically stable because, when used, they did not reveal any polymorphism, or only a very low level of it, between the original plants and the regenerants [81,82,83].”

    From Somaclonal Variation—Advantage or Disadvantage in Micropropagation of the Medicinal Plants (2023) · cites this paper as [81]

    The SSR analysis reports low polymorphism (60 of 1,324 bands, 4.49%) and concludes that the micropropagated Parmentiera cereifera plants are genetically stable. It does not say that the SSR markers themselves are genetically stable; they are the means used to assess stability. (LLM, conf=0.88)

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Research works printed but not linked: 18

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Cited by

Sorted by citations

Authors
Elshafei, A. A., & Esmaiel, N. M.
Affiliations
  • National Research Centre (EG)
  • Agricultural Research Center (EG)
Corresponding author
Elshafei, Adel Ahmed
Venue
Bulletin of the National Research Centre
Published
2018-12
Volume
42
Issue
1
ISSN
  • 1110-0591 (ISSN-L)
  • 2522-8307
OpenAlex
W2904216414
Cited by
2
References
0
Citations by year
2023: 1 · 2022: 1
FWCI
0.00
Type
journal article
Language
en
Open access
Locations
  • Bulletin of the National Research Centre/Bulletin of the National Research Center (publishedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • Greater South Information System
Funders
  • King Saud University
  • Deanship of Scientific Research, King Saud University
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant tissue culture and regeneration
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic diversity and population structure
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
Keywords
somaclonal variation, micropropagation, genetic stability, microsatellite markers, in vitro culture, shoot tip culture, axillary buds, benzyladenine, activated carbon, genetic similarity

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