Genome survey and SSR analysis of Apocynum venetum

被引:1
|
作者
Li, Guo-qi [1 ,2 ]
Song, Li-xiao [1 ,2 ]
Jin, Chang-qing [1 ,2 ]
Li, Miao [1 ,3 ]
Gong, Shi-pei [1 ,2 ]
Wang, Ya-fang [1 ,2 ]
机构
[1] Breeding Base State Key Lab Land Degradat & Ecol, Ningxia 750021, Peoples R China
[2] Minist Educ, Key Lab Restorat & Reconstruct Degraded Ecosyst N, Ningxia 750021, Peoples R China
[3] Ningxia Acad Agroforestry Sci, Ningxia 750002, Peoples R China
关键词
LEAF EXTRACT; SIZE; SEQUENCE;
D O I
10.1042/BSR20190146
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apocynum venetum is an eco-economic plant that exhibits high stress resistance. In the present paper, we carried out a whole-genome survey of A. venetum in order to provide a foundation for its whole-genome sequencing. High-throughput sequencing technology (Illumina NovaSep) was first used to measure the genome size of A. venetum, and bioinformatics methods were employed for the evaluation of the genome size, heterozygosity ratio, repeated sequences, and GC content in order to provide a foundation for subsequent whole-genome sequencing. The sequencing analysis results indicated that the preliminary estimated genome size of A. venetum was 254.40 Mbp, and its heterozygosity ratio and percentage of repeated sequences were 0.63 and 40.87%, respectively, indicating that it has a complex genome. We used k-mer = 41 to carry out a preliminary assembly and obtained contig N50, which was 3841 bp with a total length of 223949699 bp. We carried out further assembly to obtain scaffold N50, which was 6196 bp with a total length of 227322054 bp. We performed simple sequence repeat (SSR) molecular marker prediction based on the A. venetum genome data and identified a total of 101918 SSRs. The differences between the different types of nucleotide repeats were large, with mononucleotide repeats being most numerous and hexanucleotide repeats being least numerous. We recommend the use of the '2+3' (Illumina+PacBio) sequencing combination to supplement the Hi-C technique and resequencing technique in future whole-genome research in A. venetum.
引用
收藏
页数:11
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