期刊
INDUSTRIAL CROPS AND PRODUCTS
卷 36, 期 1, 页码 59-64出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.indcrop.2011.08.006
关键词
Somaclonal variation; DNA fingerprinting; Axillary branching method; Genetic stability; In vitro conservation
资金
- Ministry of Higher Education and Scientific Research
Randomly amplified polymorphic DNA markers (RAPD) were employed to assess the level of genetic stability of long term micropropagated prickly pear (Opuntia ficus-indica) plantlets. Thirteen micropropagated plantlets were chosen from a clonal collection of shoots that originated from a single mother shoot. This clonal collection had been maintained under in vitro culture conditions for at least 5 years, as achieved for the time by axillary branch multiplication in Opuntia ficus-indica. Twenty arbitrary primers were used to compare RAPD patterns between in vitro raised material and the mother plant. Only 11 primers were found to yield distinct and reproducible amplification products resulting in a total of 87 amplified products, out of which 82 bands were monomorphic across all the plantlets and 5 showed polymorphisms. Cluster analysis performed on the basis of similarity indices indicated that all micropropagated plantlets and their mother plant grouped together in one major cluster with a 91% level of similarity. Low level of genetic variation has been detected, as polymorphic bands accounted for just 2.79% of the total genetic variation. This very low level of genetic variation, despite more than 5 years of in vitro culture, demonstrates the genetic stability of Opuntia ficus-indica and indicates that the axillary branch multiplication method is highly reliable for the multiplication of genetically true-to-type plant material. The high degree of clonal fidelity detected here, recommend the use of axillary-branching micro-propagation technique for the safe in vitro conservation of prickly pear interesting genetic resources. (C) 2011 Elsevier B.V. All rights reserved.
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