Dergiler / Turkish Journal of Biology / 2015 / Cilt: 39 - Sayı: 2

Td-DAMD-PCR assays for fngerprinting of commercial carnations

Sayfa
290–298
Yayın Tarihi
2022-10-17
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Td- DAMD-PCR markers reported in this study could be very useful in species identifcation, determination of genetic relationships, andphylogenetic studies of species of Dianthus.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Dianthus L. is one of the highly valued plant species in the family Caryophyllaceae.
📊
Temel Bulgular & Veri:More than 30,000 cultivars of commercialcarnations have been recorded and there is a need for an efective and cheap method to reveal their genetic diversity and identify thecultivars.
💡
Sonuç & Katkı:Td- DAMD-PCR markers reported in this study could be very useful in species identifcation, determination of genetic relationships, andphylogenetic studies of species of Dianthus.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Dianthus L. is one of the highly valued plant species in the family Caryophyllaceae. More than 30,000 cultivars of commercialcarnations have been recorded and there is a need for an efective and cheap method to reveal their genetic diversity and identify thecultivars. To the best of our knowledge this is the frst report of implementation of the touchdown direct amplifcation of minisatellite- region DNA polymerase chain reaction (Td-DAMD-PCR) technique in the genus Dianthus. A total of 12 core minisatellite primersempirically selected from 22 primers were used in fngerprinting and phylogenetic studies of some commercial carnation cultivars.Analysis revealed that commercial carnations have a wide genetic base and they were probably obtained using inter-crosses betweenand among diferent species of the genus Dianthus. A total of 17 DNA markers were variety specifc and most of the remaining markersobtained in the present study were useful in fngerprinting of the commercial varieties studied. Commercial varieties were diferentiatedin spray and standard carnation groups in a principal coordinate analysis and a Bayesian 50% majority-rule consensus tree. Td- DAMD-PCR markers reported in this study could be very useful in species identifcation, determination of genetic relationships, andphylogenetic studies of species of Dianthus.

🔖

Bu Makaleye Atıf Yap

İNCE, A. G., KARACA, M. (2022). Td-DAMD-PCR assays for fngerprinting of commercial carnations. Turkish Journal of Biology, Cilt: 39 - Sayı: 2, 290–298. https://ajindex.com/articles/600469

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (2)

  1. Balao F, Valente LM, Vargas P, Herrera J, Talavera S (2010). Radiative evolution of polyploid races of the Iberian carnation Dianthus broteri (Caryophyllaceae). New Phytol 187: 542–551. Behroozian M, Jafari A, Farsi M (2013). RAPD analysis of genetic variation within and among natural populations of two species of Dianthus L. (Caryophyllaceae) in NE Iran. Iran J Bot 19: 194–201. Crespi A, Fernandis CF, Castro A, Berrnardos S, Amich F (2007). Morpho-environmental characterization of the genus Dianthus (Caryophylaceae) in the Iberian Peninsula: D. pungens group. Ann Bot Fenn 44: 241–255. De Benedetti L, Burchi G, Bruna S, Mercuri A, Schiva T (2003). Molecular markers and cut fower longevity in carnation. Acta Hort 683: 437–443. Farsi M, Behroozian M, Vaezi J, Joharchi MR, Memariani F (2013). Te evolution of Dianthus polylepis complex (Caryophyllaceae) inferred from morphological and nuclear DNA sequence data: one or two species? Plant Syst Evol 299: 1419–1431. Fu XP, Ning GG, Gao LP, Bao MZ (2008). Genetic diversity of Dianthus accessions as assessed using two molecular marker systems (SRAPs and ISSRs) and morphological traits. Sci Hort 117: 263–270. Heath DD, Iwama GK, Devlin RH (1993). PCR primed with VNTR core sequence yields species specifc patterns and hypervariable probes. Nucleic Acid Res 21: 5782–5785. Hosoya M (1999). Transition and trend in carnation cultivars. Agric Hort 74: 23–30 (in Japanese). Ince AG, Karaca M (2009). Te MAGi RNA extraction method: highly efcient and simple procedure for fresh and dry plant tissues. J Sci Food Agric 89: 168–176. Ince AG, Karaca M, Onus AN (2009). Development and utilization of diagnostic DAMD-PCR markers for Capsicum accessions. Genet Resour Crop Ev 56: 211–221. Ince AG, Karaca M (2011a). Genetic variation in common bean landraces efciently revealed by Td-DAMD-PCR markers. Plant Omics 4: 220–227. Ince AG, Karaca M (2011b). Early determination of sex in jojoba plant by CAPS assay. J Agri Sci 149: 327–336. Ince AG, Yildiz F, Karaca M (2011). Te MAGi DNA extraction method for fresh tissues and dry seeds. J Med Plants Res 5: 5458–5464. Ince AG, Karaca M (2012). Species-specifc touchdown DAMD-PCR markers for Salvia species. J Med Plants Res 6: 1590–1595. İnce AG, Karaca M (2014) E-microsatellite markers for some Salvia species naturally occurring in the Mediterranean region. Turk J Biol doi: 10.3906/biy-1404-29.
  2. Ince AG, Karaca M, Elmasulu SY (2014). New microsatellite and CAPS-microsatellite markers for clarifying