Evidence map›Paper›PMID 21253894›Full record

ArticleMolecular biotechnology2011

Genetic relationship of Curcuma species from Northeast India using PCR-based markers.

Archana Das, Vigya Kesari, Vinod M Satyanarayana, Ajay Parida, Latha Rangan

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Article in Molecular biotechnology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Genetic Diversity of Torch Ginger (BioMed research international · 2019
    Article
  5. Review
  6. Assessment of genetic diversity in indigenous turmeric (Curcuma longa) germplasm from India using molecular markers.Physiology and molecular biology of plants : an international journal of functional plant biology · 2015
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Assessment of phylogenetic relationship among twentyJournal of advanced pharmaceutical technology & research
    Article
4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Archana DasDepartment of Biotechnology, Indian Institute of Technology Guwahati, North Guwahati, 781 039, Assam, India.
Vigya Kesari
Vinod M Satyanarayana
Ajay Parida
Latha Rangan

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular genetic fingerprints of nine Curcuma species from Northeast India were developed using PCR-based markers. The aim involves elucidating there intra- and inter-specific genetic diversity important for utilization, management, and conservation. Twelve random amplified polymorphic DNA (RAPD), 19 Inter simple sequence repeats (ISSRs), and four amplified fragment length polymorphism (AFLP) primers produced 266 polymorphic fragments. ISSR confirmed maximum polymorphism of 98.55% whereas RAPD and AFLP showed 93.22 and 97.27%, respectively. Marker index and polymorphic information content varied in the range of 8.64-48.1, 19.75-48.14, and 25-28 and 0.17-0.48, 0.19-0.48, and 0.25-0.29 for RAPD, ISSR, and AFLP markers, respectively. The average value of number of observed alleles, number of effective alleles, mean Nei's gene diversity, and Shannon's information index were 1.93-1.98, 1.37-1.62, 0.23-0.36, and 0.38-0.50, respectively, for three DNA markers used. Dendrograms based on three molecular data using unweighted pair group method with arithmetic mean (UPGMA) was congruent and classified the Curcuma species into two major clusters. Cophenetic correlation coefficient between dendrogram and original similarity matrix were significant for RAPD (r = 0.96), ISSR (r = 0.94), and AFLP (r = 0.97). Clustering was further supported by principle coordinate analysis. High genetic polymorphism documented is significant for conservation and further improvement of Curcuma species.

Indexed as

Genetic MarkersAllelesAmplified Fragment Length Polymorphism AnalysisCurcumaDNA, PlantDNA PrimersIndiaMicrosatellite RepeatsMultigene FamilyPolymorphism, GeneticRandom Amplified Polymorphic DNA TechniqueDNA, PlantDNA PrimersGenetic Markers

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.