In this study, a total of sixteen RAPD primers were used for evaluation of the genetic diversity of eight H. serrata samples collected from different locations of Sa Pa and Da Lat. Overall, sixteen markers generated a total of 70 fragments in 8 collected samples of H. serrata. Of seventy generated fragments, 44 were found to be polymorphic. | Evaluation of the genetic diversity of Huperzia serrate by rapd markers ACADEMIA JOURNAL OF BIOLOGY 2018, 40(4): 85–90 DOI: EVALUATION OF THE GENETIC DIVERSITY OF Huperzia serrate BY RAPD MARKERS Ho Thi Huong1, Ngo Thi Thuy Linh1, Le Thi Lan Anh2, Le Thi Bich Thuy1, 2* 1 Institute of Biotechnology, VAST 2 Graduate University of Science and Technology, VAST ABTRACT Huperzia serrata, a valuable pharmaceutical plant distributed in Lao Cai (Northwest Vietnam) and Lam Dong (Central Highlands of Vietnam), is known as pharmaceutical material for the treatment of Alzheimer’s disease. As the result of over-exploitation and habitat fragmentation, H. serrata has become a threatened plant in Vietnam, China and other countries around the world. For the understanding of population dynamics, adaptation, evolution and conservation of plant species in general and H. serrata in particular, the evaluation of genetic diversity is very important. In this study, the total of 16 RAPD primers were used for evaluation of the genetic diversity of eight H. serrata samples collected from different locations of Sa Pa and Da Lat. Overall, 16 markers generated a total of 70 fragments in eight collected samples of H. serrata. Of 70 generated fragments, 44 were found to be polymorphic. The number of fragments of each primer ranged from 1 to 8 with an average of 4,4 fragments per primer. The OPB20 primer revealed the highest polymorphism, while the OPB15, OPB17 and OPC12 primers gave the lowest. Polymorphism information content (PIC) values varied from to with an average of , in which the highest value belonged to OPB11 primer while the OPC10 primer showed the lowest PIC value. The dendrogram created based on RAPD data sheet divided the investigated strain into two major groups corresponding to their habitat: Group I included three Da Lat samples (DL1, DL2, DL3) and Group II .
