| Literature DB >> 33175097 |
Kenji Nashima1, Kenta Shirasawa2, Andrea Ghelfi2, Hideki Hirakawa2, Sachiko Isobe2, Takuro Suyama3, Takuya Wada3, Takeshi Kurokura4, Tatuya Uemachi5, Mirai Azuma1, Midori Akutsu6, Masaharu Kodama6, Yoshiko Nakazawa6, Kiyoshi Namai6.
Abstract
Owing to its high ornamental value, the double flower phenotype of hydrangea (Hydrangea macrophylla) is one of its most important traits. In this study, genome sequence information was obtained to explore effective DNA markers and the causative genes for double flower production in hydrangea. Single-molecule real-time sequencing data followed by a Hi-C analysis were employed. Two haplotype-phased sequences were obtained from the heterozygous genome of hydrangea. One assembly consisted of 3,779 scaffolds (2.256 Gb in length and N50 of 1.5 Mb), the other also contained 3,779 scaffolds (2.227 Gb in length, and N50 of 1.4 Mb). A total of 36,930 genes were predicted in the sequences, of which 32,205 and 32,222 were found in each haplotype. A pair of 18 pseudomolecules was constructed along with a high-density single-nucleotide polymorphism (SNP) genetic linkage map. Using the genome sequence data, and two F2 populations, the SNPs linked to double flower loci (djo and dsu) were discovered. DNA markers linked to djo and dsu were developed, and these could distinguish the recessive double flower allele for each locus, respectively. The LEAFY gene is a very likely candidate as the causative gene for dsu, since frameshift was specifically observed in the double flower accession with dsu.Entities:
Keywords: zzm321990 de novo genome sequencing; DNA marker; double flower; hydrangea
Mesh:
Year: 2021 PMID: 33175097 PMCID: PMC7934569 DOI: 10.1093/dnares/dsaa026
Source DB: PubMed Journal: DNA Res ISSN: 1340-2838 Impact factor: 4.458