首页|基于LFY2int2和SSR的浙江云和梨种质鉴定

基于LFY2int2和SSR的浙江云和梨种质鉴定

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[目的]明确浙江云和梨地方品种的遗传背景,为优良品种选育提供科学依据.[方法]基于低拷贝核基因LFY2int2的DNA序列和SSR对16份云和梨种质进行了分子鉴定.[结果]供试样本中共有4种LFY2int2拷贝(a,b1,b2和c),除了‘真香梨1’(c/b2)和‘云和红梨’(b1/b2)外,其余样本均为a/b1.基于LFY2int2的系统发育树表明‘真香梨1’与所有中国砂梨(Pyrus pyrifolia)样本分开独立成支;12对SSR引物在供试样本中分别扩增出了2~6个等位基因,UPGMA聚类结果显示‘真香梨1’和‘云和红梨’分别以0.45和0.70的相似系数与其他云和梨样本分开,而其余样本可分为2组,其中‘老雪梨4’和‘薄皮雪梨2’一致,‘老雪梨3’和‘老雪梨10’一致.[结论]基于LFY2int2和SSR的分析结果表明‘真香梨1’与中国砂梨亲缘关系远,它可能是砂梨和西洋梨(P.communis)的杂交后代;‘云和红梨’与典型云和雪梨起源不同;此外鉴定出了2组可能为同物异名的种质.
Identification of Yunhe pears in Zhejiang province based on LFY2int2 and SSR analyses
[Objective] Yunhe pears are a group of Chinese sand pears (Pyrus pyrifolia) native to Lishui,Zhejiang province,China and can be divided into two types,Laoxueli and Zhenxiangli,which are important and unique germplasm resources for their large fruits and/or lateness in ripening compared with the current sand pear cultivars.Some fine selections of Yunhe pears were collected and planted under unified conditions as candidates for selection and breeding.However,some of these selections showed a high level of similarity on morphological characteristics and phenological phases,suggesting the possibility of synonyms.So far,little has been known about the genetic background of Yunhe pears,especially Zhenxiangli.To provide a basis for the breeding of Yunhe pear cultivars,their genetic background and relationships among these fine selections needs to be estimated.[Methods] Eleven fine selections of Laoxueli and one Zhenxiangli accession were collected from Yunhe and Jingning in Lishui,grafted onto ‘Cuiguan’ and grown under uniform conditions.One semi-wild accession,‘ YHHL’,and three other Laoxueli accessions (‘XHXL’,‘BPXL1’ and ‘BPXL2’) were collected from local orchards.Young leaves of these 16 accessions were collected and the total genomic DNA was extracted by using CTAB methods for the following PCRs.The second intron of the LEAFY2 gene,LFY2int2,was amplified by using primers of LFY2-F and LFY2-R.The PCR products were directly sequenced,and more than three TA clones were sequenced when there were intra-individual divergent copies.The LFY2int2 sequences of Chinese sand pears and Meili native to Zhejiang province and P.betuleaforlia obtained in our previous study were aligned with sequences obtained in this study using Clustal X.Phylogenetic trees based on Maximum Parsimony methods were constructed using MEGA6 with sequence of Malus domestica (GenBank accession number DQ535886) as an outgroup.12 SSR markers explored in previous studies were selected.NH026a,CH02b10,CH01b12 and CH01f02 were genomic SSRs,and each forward primer was fluorescently-labeled by Fam (blue) or Hex (green).The other 8 markers were explored from pear transcriptomes and the primer pairs were provided by the explorer,each forward primer was added by a tail (M 13 universal sequence) to the 5’ end,and the additional primer M13 was fluorescently-labeled by Farm or Hex.The PCR and sequencing of the SSRs were carried out according to the referenced studies.The number of alleles,expected heterozygosity (He),observed heterozygosity (Ho) and polymorphism information content (PIC) were calculated by using MStool.The sequencing results of the marker length (bp value) were transformed into a 0/1 value by DataTrans,then a dendrogram using UPGMA (unweighted pair-group method with arithmetic average) cluster analysis based on DICE identity was constructed by NTSYSYpc 2.02.[Results] Direct sequencing of LFY2int2 PCR products showed that ‘YHHL’ had one overlapped site,while ‘Zhenxiangli’ had six,so TA cloning was carried out for ‘Zhenxiangli’ The other 14 accessions shared the same results with multiple overlapped sites and one indel at site 480 bp,and two accessions,‘ Laoxueli l’ and ‘ Laoxueli 3’,were randomly selected for TA cloning.As a result,four distinct LFY2int2 copies (a,b1,b2,c) were observed among the 16 accessions.Alignment of these four copies produced 11 substitutions and one indel,and copy b1 and b2 had only one substitution difference.‘YHHL’ had two copies of b1 and b2,‘Zhenxiangli’ had c and b2,and the other accessions had copies a and b1.The phylogenetic tree based on the LFY2int2 sequences showed that copy c of ‘Zhenxiangli 1’ formed a separating clade,while b1 and b2 were in clade Ⅰ with Chinese sand pears such as ‘Yiwulizi’ and ‘Puguali’ and the copy a from Laoxueli was in clade Ⅱ with two copies from Meili,which belong to the paralog of the LFY2int2-Del2 copy types.Among the 12 SSR markers,only TXY77 failed in amplification of five accessions.Each primer pair produced 2 to 6 alleles,and the He was from 0.062 5 to 0.688 3,the Ho was from 0.062 5 to 1,and the PIC was from 0.058 7 to 0.707 3.Among the markers,8 showed a low level of polymorphisms,which could only discriminate ‘Zhenxiangli’ and/or ‘YHHL’ from the other 16 accessions.The dendrogram of the 16 Yunhe pear accessions based on UPGMA showed that ‘Zhenxiangli’ and ‘YHHL’ were separated from the other accessions at the coefficient of 0.45 and 0.7,respectively,while the rest accessions were clustered into two groups.Group 1 consists of six Laoxueli accessions including four fine individuals,‘XHXL’ and ‘ BPXL’ in group 2,there were eight accessions,among which ‘Laoxueli4’ and ‘ Bopixueli2’ were identical,while ‘ Laoxueli3’ and ‘Laoxueli10’ were identical.[Conclusion] Phylogenetic analyses based on LFY2int2 sequences suggested that Laoxueli and the unknown ‘YHHL’ belonged to the Chinese sand pear,while ‘ Zhenxiangli’ which had the special c copy types,did not.The dendrogram based on SSRs showed that ‘Zhenxiangli’ and ‘YHHL’ were not genetically closely related to Laoxueli accessions,and two sections of the putative synonyms were identified.According to their morphological characteristics,‘Zhenxiangli’ was possibly a hybrid between the Chinese sand pear and P.communis,which is worth further study by investigating the local cultivars of P.communis.

Yunhe pearLFY2int2SSRSelection and breeding

郑小艳、杨舒贻、周晓音、潘芝梅

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丽水学院,浙江丽水323000

丽水市农作物站,浙江丽水323000

丽水职业技术学院,浙江丽水323000

云和梨 LFY2int2 SSR 品种选育

浙江省自然科学基金云和传统雪梨优系选育云和传统雪梨优系选育丽水学院校级学生科研项目丽水水果产业科技创新团队

LQ13C0200011期2014XPZ042013年34号2012cxtd07

2016

果树学报
中国农业科学院郑州果树研究所

果树学报

CSTPCDCSCD北大核心
影响因子:1.486
ISSN:1009-9980
年,卷(期):2016.33(6)
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