2010
DOI: 10.3732/ajb.1000096
|View full text |Cite
|
Sign up to set email alerts
|

Characterization of nuclear microsatellite loci in the Neotropical tree Parkia panurensis (Fabaceae)

Abstract: All nine loci could also be verified in six other Parkia species and polymorphic fragments amplified. The new marker set can be used for future studies of genetic diversity and differentiation, as well as estimation of gene flow and parentage analyses in various Parkia species.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
3
0

Year Published

2012
2012
2024
2024

Publication Types

Select...
4

Relationship

2
2

Authors

Journals

citations
Cited by 4 publications
(4 citation statements)
references
References 7 publications
(6 reference statements)
0
3
0
Order By: Relevance
“…We used nine highly polymorphic nuclear microsatellite loci for genotyping (Luettmann et al 2010). PCR and genotyping methods are reported in detail in Heymann et al (2012).…”
Section: Molecular Genetic Methods and Analyses Of Genetic Variationmentioning
confidence: 99%
“…We used nine highly polymorphic nuclear microsatellite loci for genotyping (Luettmann et al 2010). PCR and genotyping methods are reported in detail in Heymann et al (2012).…”
Section: Molecular Genetic Methods and Analyses Of Genetic Variationmentioning
confidence: 99%
“…For the extraction of DNA, hexadecyltrimethylammonium bromide CTAB protocol was used as described by [21] and then quantified [17]. A total of 9 polymorphic and informative microsatellite primers developed for Parkia panurensis (Parpan 3, Parpan 4, Parpan 5, Parpan 9, Parpan11, Parpan13, Parpan14, Parpan15, and Parpan 21) (Table 1) were validated in heterologous amplification [22] and were used in the study. These microsatellite loci were amplified by polymerase chain reaction (PCR) using a Veriti thermal cycler (Applied Biosystems, Foster City, CA, USA) with a total volume of 10 µL per reaction (containing 10 ng of genomic DNA, 1× buffer, 210 µM of each dNTP, 1.5 mM MgCl 2 , 0.16 µM forward primer and M13 (FAM or NED) broth [23], 0.32 µM reverse primer, 1.05 U Taq DNA polymerase (Invitrogen, Carlsbad, CA, USA), and 3.49 µL ultrapure water.…”
Section: Amplification Of Microsatellite Markersmentioning
confidence: 99%
“…For DNA fingerprinting all seed coat and leaf samples were analysed at seven highly polymorphic nuclear microsatellite (nSSR) loci, previously characterised in Parkia panurensis : Parpan3, Parpan4, Parpan5, Parpan9, Parpan14, Parpan15, Parpan21 [40]. PCR amplifications were carried out in a Thermocycler (Biometra, Göttingen, Germany) using fluorescent labelled primers.…”
Section: Methodsmentioning
confidence: 99%
“…PCR amplifications were carried out in a Thermocycler (Biometra, Göttingen, Germany) using fluorescent labelled primers. PCR protocols are specified in [40]. Numbers of cycles were increased for the seed coats following the procedure with other exocarp material [41].…”
Section: Methodsmentioning
confidence: 99%