Germplasm collections are a crucial resource to conserve natural genetic diversity and provide a source of novel traits essential for sustained crop *** collection,preservation and utilization of these materials depen...
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Germplasm collections are a crucial resource to conserve natural genetic diversity and provide a source of novel traits essential for sustained crop *** collection,preservation and utilization of these materials depends upon knowledge of the genetic variation present within the *** we use the high-throughput genotyping-by-sequencing(GBS)technology to characterize the United States national plant Germplasm System(NPGS)collection of cucumber(Cucumis sativus L.).The GBS data,derived from 1234 cucumber accessions,provided more than 23 K high-quality single-nucleotide polymorphisms(SNPs)that are well distributed at high density in the genome(~1 SNP/10.6 kb).The SNP markers were used to characterize genetic diversity,population structure,phylogenetic relationships,linkage disequilibrium,and population differentiation of the NPGS cucumber *** results,providing detailed genetic analysis of the *** collection,complement NPGS descriptive information regarding geographic origin and phenotypic *** also identified genome regions significantly associated with 13 horticulturally important traits through genome-wide association studies(GWAS).Finally,we developed a molecularly informed,publicly accessible core collection of 395 accessions that represents at least 96%of the genetic variation present in the ***,the information obtained from the GBS data enabled deep insight into the diversity present and genetic relationships among accessions within the collection,and will provide a valuable resource for genetic analyses,gene discovery,crop improvement,and germplasm preservation.
[Objective]The paper was to develop the microsatellite markers of Datnioides pulcher,and to screen polymorphic SSR primers.[Method]*** was performed reduced-representation genome sequencing using RAD-seq(Restriction-s...
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[Objective]The paper was to develop the microsatellite markers of Datnioides pulcher,and to screen polymorphic SSR primers.[Method]*** was performed reduced-representation genome sequencing using RAD-seq(Restriction-site associated DNA sequencing).[Result]A total of 13308806 high-quality clean reads(HQ clean reads)lengths were obtained and 26359 simple sequence repeats(SSR)loci were detected in the obtained sequence by SSR search software,which consisted of 496 repeat *** most common types of repeat were A/T in single base repeat sequence,and AC/GT and A G/GT repeat units in di-base repeat ***/CCT,AGC/CTG and AGG/CCT were the dominant types in tri-base repeat *** quantity,the di-base repeat type SSR loci were the largest(19492),accounting for 73.95%of the total SSR *** for mono-nucleotide type,the repetition frequency of SSR loci was mainly ranged from 4 to 9,and the number of polymorphic SSR loci was *** 20066 pairs of SSR primers were successfully designed with Primer *** success rate of primer design was 76.13%.According to the repetition type and repetition number in the sequencing data,100 di-to penta-base repetition type SSRs were randomly selected and validated by PCR and polyacrylamide gel in six *** samples.A total of 73 pairs of primers were amplified by electrophoresis,and 20 of them were polymorphic.[Conclusion]The developed SSR sequences can be used for genetic analysis,genetic map construction and molecular marker assisted breeding of *** and its related species.
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