TY - JOUR
T1 - Genome sequence of Hydrangea macrophylla and its application in analysis of the double flower phenotype
AU - Nashima, Kenji
AU - Shirasawa, Kenta
AU - Ghelfi, Andrea
AU - Hirakawa, Hideki
AU - Isobe, Sachiko
AU - Suyama, Takuro
AU - Wada, Takuya
AU - Kurokura, Takeshi
AU - Uemachi, Tatuya
AU - Azuma, Mirai
AU - Akutsu, Midori
AU - Kodama, Masaharu
AU - Nakazawa, Yoshiko
AU - Namai, Kiyoshi
N1 - Publisher Copyright:
© 2020 The Author(s). Published by Oxford University Press on behalf of Kazusa DNA Research Institute.
PY - 2021/2/1
Y1 - 2021/2/1
N2 - 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.
AB - 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.
KW - DNA marker
KW - De novo genome sequencing
KW - Double flower
KW - Hydrangea
UR - http://www.scopus.com/inward/record.url?scp=85102222677&partnerID=8YFLogxK
U2 - 10.1093/dnares/dsaa026
DO - 10.1093/dnares/dsaa026
M3 - Article
C2 - 33175097
AN - SCOPUS:85102222677
SN - 1340-2838
VL - 28
JO - DNA Research
JF - DNA Research
IS - 1
M1 - dsaa026
ER -