Scientia Agricultura Sinica ›› 2020, Vol. 53 ›› Issue (16): 3333-3343.doi: 10.3864/j.issn.0578-1752.2020.16.011

• HORTICULTURE • Previous Articles     Next Articles

Genetic Relationship and Structure Analysis of 15 Species of Malus Mill. Based on SNP Markers

GAO Yuan(),WANG DaJiang,WANG Kun(),CONG PeiHua(),LI LianWen,PIAO JiCheng   

  1. Institute of Pomology, Chinese Academy of Agricultural Sciences/Key Laboratory of Horticultural Crops Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs of the People’s Republic of China, Xingcheng 125100, Liaoning
  • Received:2019-12-30 Accepted:2020-06-10 Online:2020-08-16 Published:2020-08-27
  • Contact: Kun WANG,PeiHua CONG E-mail:gaoyuan02@caas.cn;wangkun5488@163.com;congph@163.com

Abstract:

【Objective】 Based on SNP markers developed by high-throughput, the simplified genomic sequencing technology in the whole genome, the genetic relationship and population genetic structure of native germplasms of Malus Mill. in China were analyzed, which provided a theoretical basis for the origin, evolution and systematic classification of Malus Mill.【Method】Based on obtained SLAF tags, BWA software was used to locate them in the reference genome and to obtain the polymorphic SLAF tags. GATK and SAMtool were employed to develop SNPs in polymorphic SLAF tags and screened SNPs obtained by two methods as SNP markers data set. According to the integrity > 0.94 and the minor allele frequency (MAF) > 0.05, SNPs with polymorphism were screened. Based on the screening of polymorphic SNPs, the NJ (neighbor joining) algorithm of MEGA 7 was used to construct phylogenetic trees of different species of Malus Mill. The genetic structure was analyzed by using the software of admixture. Assuming that the number of clusters (k) was 1-15. The best K value was determined according to cross validation error rate, and the genetic structure among and within species of Malus Mill. was analyzed.【Result】427 accessions of Malus Mill. were sequenced by SLAF-seq, and 586 454 SLAF tags were obtained, including 463 612 polymorphic SLAF tags. 46 460 polymorphic single nucleotide (SNP) loci were obtained through sequence alignment analysis and screening. Phylogenetic tree of different species of Malus Mill. was constructed based on these SNP loci, and population structure was analyzed. In phylogenetic analysis, 15 species of Malus Mill. were divided into 4 groups, and K = 5 and K = 14 were key points in the genetic structure analysis. According to the results of two methods, 15 species of Malus Mill. could be divided into 4 basic groups, which were the group of Malus baccata, the group of Malus sieversii and a few accessions of Malus domestica subsp.chinensis, the group of Malus toringoides, Malus transitoria, Malus kansuensis, Malus komarovii, Malus yunnanensis and Malus ombrophila, and the group of Malus domestica subsp. chinensis, Malus robusta, Malus asiatica and Malus prunifolia. There were gene backgrounds of Malus sieversii and Malus baccata in some germplasms of Malus domestica subsp. chinensis, but there were also some germplasms of Malus domestica subsp. Chinensis, which could independently represent the group gene pool, and the gene pool was not involved in Malus sieversii, but closely related to Malus baccata, Malus asiatica and Malus prunifolia.【Conclusion】The rapid discovery of 46 460 polymorphic SNP markers covering the whole genome by SLAF technology could effectively study on the genetic relationship and structure within and among species of Malus Mill. in China, and provide references for identification and evaluation, genetic diversity, systematic classification, origin and evolution of germplasm resources of Malus Mill. 15 species of Malus Mill. could be divided into 4 basic groups, and the classification of wild and cultivated species of Malus Mill. was obvious. The genetic relationship between Malus domestica subsp. chinensis and other cultivated species was close.

Key words: Malus Mill., SNP, genetic relationship, genetic structure

Table 1

Fifteen species of Malus Mill. germplasm resources for SLAF-seq analysis"

序号
Code
供试种
Species
来源地
Origin
数量
Number
序号
Code
供试种
Species
来源地
Origin
数量
Number
1 新疆野苹果 Malus sieversii 新疆 Xinjiang 161 5 花红 Malus asiatica 黑龙江 Heilongjiang 7
2 中国苹果
Malus domestica subsp.chinensis
新疆 Xinjiang 2 甘肃 Gansu 1
黑龙江 Heilongjiang 2 河北 Hebei 9
甘肃 Gansu 4 云南 Yunnan 1
河北 Hebei 14 6 八棱海棠 Malus robusta 河北 Hebei 32
山西 Shanxi 10 山西 Shanxi 1
山东 Shandong 1 吉林 Jilin 1
3 山荆子 Malus baccata 黑龙江 Heilongjiang 47 7 陇东海棠 Malus kansuensis 甘肃 Gansu 4
甘肃 Gansu 3 8 垂丝海棠 Malus halliana 甘肃 Gansu 9
河北 Hebei 10 9 山楂海棠 Malus komarovii 吉林 Jilin 1
山西 Shanxi 14 10 变叶海棠 Malus toringoides 四川 Sichuan 2
内蒙古 Inner Mongolia 41 云南 Yunnan 1
吉林 Jilin 19 11 花叶海棠 Malus transitoria 四川 Sichuan 1
4 楸子 Malus prunifolia 黑龙江 Heilongjiang 5 12 丽江山荆子 Malus rockii 云南 Yunnan 1
甘肃 Gansu 4 13 滇池海棠 Malus yunnanensis 云南 Yunnan 1
河北 Hebei 2 14 湖北海棠 Malus hupehensis 云南 Yunnan 1
山西 Shanxi 8 15 沧江海棠 Malus ombrophila 云南 Yunnan 1
内蒙古 Inner Mongolia 1
吉林 Jilin 5

Fig. 1

The distribution of polymorphic SNP in 17 chromosomes Every yellow band indicated one chromosome, and black line indicated the position of SNP. The abscissa is the length of the chromosome, and the genome was divided by every 1M. The darker position represented more SNPs, and the darker regions showed the centralized distribution area of SNPs"

Table 2

Genetic distance of 15 species of Malus Mill. based on SNP"

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15
1 0.000
2 0.030 0.000
3 0.970 1.000 0.000
4 0.600 0.606 0.394 0.000
5 0.030 0.000 1.000 0.606 0.000
6 0.030 0.000 1.000 0.606 0.000 0.000
7 0.030 0.000 1.000 0.606 0.000 0.000 0.000
8 0.187 0.167 0.833 0.571 0.167 0.167 0.167 0.000
9 0.030 0.000 1.000 0.606 0.000 0.000 0.000 0.167 0.000
10 0.953 0.981 0.019 0.398 0.981 0.981 0.981 0.821 0.981 0.000
11 0.143 0.120 0.880 0.581 0.120 0.120 0.120 0.247 0.120 0.866 0.000
12 0.030 0.000 1.000 0.606 0.000 0.000 0.000 0.167 0.000 0.981 0.120 0.000
13 0.134 0.111 0.889 0.582 0.111 0.111 0.111 0.241 0.111 0.874 0.204 0.111 0.000
14 0.279 0.265 0.735 0.550 0.265 0.265 0.265 0.343 0.265 0.727 0.321 0.265 0.317 0.000
15 0.030 0.000 1.000 0.606 0.000 0.000 0.000 0.167 0.000 0.981 0.120 0.000 0.111 0.265 0.000

Fig. 2

Polygenetic tree of 15 species of Malus Mill. based on SNP"

Fig. 3

Cross validation error rates corresponding to every K values"

Fig. 4

The genetic structure of 427 accessions of 15 species of Malus Mill. (K=5 and K=14) Each bar represents one accession, and the abscissa is the code of germplasms corresponding to each bar. One color represents one group, and the ordinate is Q value 0.00-1.00"

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