Clonal micropropagation of Pistacia lentiscus L. and assessment of genetic stability using IRAP markers

Plant Growth Regulation - Tập 75 - Trang 75-88 - 2014
Fatih Mehmet Kılınç1, Veysel Süzerer2, Yelda Özden Çiftçi3, Ahmet Onay1, Hakan Yıldırım4, Ahu Altınkut Uncuoğlu5, Engin Tilkat6, İbrahim Koç3, Ömer Faruk Akdemir1, Özge Karakaş Metin7
1Department of Biology, Faculty of Science, Dicle University, Diyarbakır, Turkey
2Medical Laboratory, Vocational School of Health Services, Bingöl University, Bingöl, Turkey
3Department of Molecular Biology and Genetics, Gebze Institute of Technology, Gebze, Turkey
4Department of Horticulture, Faculty of Agriculture, Dicle University, Diyarbakır, Turkey
5Department of Bioengineering, Faculty of Engineering, Marmara University, Göztepe, Turkey
6Department of Biology, Faculty of Science and Literature, Batman University, Batman, Turkey
7Marmara Research Center, Genetic Engineering and Biotechnology Institute, TÜBİTAK, Gebze, Turkey

Tóm tắt

An efficient protocol for clonal micropropagation of selected genotypes of lentisk, Pistacia lentiscus L., which is cultivated for the masticha resin, has been developed using shoot tip explants originating from in vitro seedlings. BA was found to be optimum for shoot morphogenesis in terms of the number and length of shoots among the cytokinins tested for all cloned genotypes, while the highest shoot length was noticed in the presence of 2iP at a rate 4.92 µM. Efficient rooting (94.15 %) was achieved in a medium containing 19.6 µM IBA with the clone II that was superior to the rest of the clones tested. The method developed for plant acclimatization was satisfactory because a high percentage of plant survival (95 %) in the growth room in the clone II was obtained and the regenerated plantlets resumed growth after 4 months. DNAs from mother seedlings and micropropagated plantlets belonging to 6, 9 and 12 times subcultured were isolated and subjected to IRAP analysis in order to evaluate their genetic stability and detect possibly existing variations among in vitro derived plantlets. The mean percentage of similarity calculated by Jaccard’s similarity coefficient ranged from 78 to 86 % in the four genotypes. Although variation was observed among mother plantlets and its regenerants for all of the clones, polymorphic information content value in the range of 0.391–0.405 indicated the presence of reasonable polymorphism within the clones. The presented data confirmed that the clonal propagation of lentisk by using shoot tips could be used for commercial exploitation of the selected genotype.

Tài liệu tham khảo

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