Ontology highlight
ABSTRACT: Premise of the study
Hamamelis mollis (Hamamelidaceae) is a Tertiary relict species endemic to southern China. Polymorphic microsatellite markers were developed to reveal the genetic diversity of this species.Methods and results
The genome of H. mollis was sequenced and de novo assembled into 642,351 contigs. A total of 72,097 paired primers were successfully designed from 80,282 simple sequence repeat (SSR) markers identified in 63,419 contigs. PCR amplification showed that 96 of the 136 synthesized primers could be successfully amplified, and 22 demonstrated polymorphism. The mean number of alleles, levels of observed heterozygosity, and levels of expected heterozygosity were 4.602 ± 0.140, 0.632 ± 0.020, and 0.696 ± 0.010, respectively. The majority of the 96 primer pairs could be amplified in at least one other Hamamelidaceae species, including Distylium myricoides (60), Loropetalum chinense (39), Exbucklandia populnea (24), and E. tonkinensis (24).Conclusions
These microsatellite loci provide abundant genomic SSR markers to evaluate genetic diversity of this woody ornamental plant.
SUBMITTER: Yin Q
PROVIDER: S-EPMC6201723 | biostudies-literature | 2018 Oct
REPOSITORIES: biostudies-literature
Applications in plant sciences 20181023 10
<h4>Premise of the study</h4><i>Hamamelis mollis</i> (Hamamelidaceae) is a Tertiary relict species endemic to southern China. Polymorphic microsatellite markers were developed to reveal the genetic diversity of this species.<h4>Methods and results</h4>The genome of <i>H. mollis</i> was sequenced and de novo assembled into 642,351 contigs. A total of 72,097 paired primers were successfully designed from 80,282 simple sequence repeat (SSR) markers identified in 63,419 contigs. PCR amplification sh ...[more]