African Journal of
Biotechnology

  • Abbreviation: Afr. J. Biotechnol.
  • Language: English
  • ISSN: 1684-5315
  • DOI: 10.5897/AJB
  • Start Year: 2002
  • Published Articles: 12500

Full Length Research Paper

LTR-retrotransposons-based molecular markers in cultivated Egyptian cottons G. barbadense L.

Elsayed E. Hafez1F, Abdel Ghany A. Abdel Ghany2F and Essam A. Zaki1*   FThese authors contributed equally to this work.
1Nucleic Acids Research Department, Genetic Engineering and Biotechnology Research Institute, GEBRI, Research Area, Borg El Arab, Post Code 21934, Alexandria. 2Institute of Efficient Productivity, Zagazig University, El Zagazig, Egypt.
Email: [email protected]

  •  Accepted: 05 May 2006
  •  Published: 03 July 2006

Abstract

Long terminal repeat (LTR)-retrotransposons are mobile genetic elements that are ubiquitous in plants and constitute a major portion of their nuclear genomes. LTR-retrotransposons possess unique properties that make them appropriate for investigating relationships between closely related species and populations. The aim of the current study was to employ Ty1-copia group retrotransposons as molecular markers in cultivated Egyptian cottons, G. barbadense L. Restriction site analysis of PCR-amplified Ty1-copia RT domain promoted the construction of a restriction map for each Egyptian cultivar. These maps display distinctive patterns of restriction site variation. Furthermore, these patterns are capable of differentiating even between cultivars that appear to have diverged only in the past 50 years. These results demonstrate that retrotransposon-based molecular markers are particularly valuable tools for plant molecular phylogenetic and population genetic studies.

 

Key words: DNA fingerprinting, Gossypium, repetitive DNA, restriction site polymorphisms, sequence diversity, Ty1-copia group retrotransposons.

Abbreviation

IN, integrase; LTR, long terminal repeat; PCR, polymerase chain reaction; RT, reverse transcriptase gene

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This article is published under the terms of the Creative Commons Attribution License 4.0

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