462
The 3
rd
International Symposium on EuroAsian Biodiversity
05-08 July 2017, Minsk - BELARUS
PP-274
Molecular Phlogeny of Acantholimon Boiss. (Plumbaginaceae) Genus from Turkey
Related TRN and ITS Regions
Feyza CANDAN
1
, Tuna UYSAL
2
, Musa DOĞAN
3
, Meryem BOZKURT
2,4
1
Department of Biology, Faculty of Science and Arts, Manisa Celal Bayar University,
Manisa, Turkey
2
Department of Biology,Faculty of Science, Selçuk University, Konya, Turkey
3 Department of Biological Sciences, Faculty of Science and Arts, Middle East Technical
University, Ankara, Turkey
4
Advanced Technology Research and Application Center, Selçuk University, Konya, Turkey
feyzacandan2002@yahoo.com
Aim of the study:
The impact of molecular phylogenetic studies on plants have raised in the
meantime development of technology in the light of
high explanations regarding
relationships. According to this study,
Acantholimon
genus has
selected to find out its
molecular phlogeny by using TRN and ITS primers. According to this study,
it is aimed to
reveal molecular phlogeny of
Acantholimon
genus by using TRN and ITS primers related 62
taxa of
Acantholimon
genus, which of 42 are endemic, collected
from Turkey by preparing
dendrograms and making analysis.
Material and Methods:
62 taxa of
Acantholimon
genus were
gathered from all over the
Turkey at their flowering times. Specimens were kept as herbarium materials. Flora of Turkey
was used for their taxonomical description. On the other hand, DNA isolation was made by
using Qiagen DNeasy Plant Mini Kit. After DNA deriving, bioanalyzer instrument was used to
measure their A260/280 rate (purity evaluation) and determine the quality of DNA. However,
agarose jel photographs were taken after PCR reactions.
TRNc-d and ITS 4b-5a primers were selected for this investigation from the literature checks.
TRNc: CGA AAT CGG TAG ACG CTA CG, 40 nmol
TRNd: GGG GAT AGA GGG ACT TGA AC, 40 nmol
ITS 4b: TCCTCCGCTTATTGATATGC,20 nmol
ITS 5a: GGAAGGAGAAGTCGTAACAAGG,20 nmol
Cycle sequencing and purity studies of PCR materials after cycle sequencing were made.
After all these gradations, DNA sequence analyses were made in a detailed way.
Results:
Molecular phlogeny of
Acantholimon
genus tried to reveal with the primers as TRN
c-d region of the chloroplast DNA and ITS 4b-5a region of the nucleus DNA. As a result of
the study, it is determined the relationships between taxa according to genus. 6 dendrograms
by using TRN, ITS and
both TRN-ITS sequences were
made with ‘Maximum Possibilty
Analysis’ and ‘Parsimony Analysis’ to reveal relation degrees according to taxa of genus and
comparisons were made. Network analysis was made by
using TRN and ITS data to
understand geographic distribution of the genus.
Acknowledgements:
The authors would like to thank the Scientific and Technical Research
Council of Turkey (TUBITAK) for projects funding (TBAG-1781 and 212T222).
Keywords: Acantholimon
, TRN, ITS, molecular phlogeny.