首页|基于SSR标记的'黑果枸杞'F1代群体杂种鉴定及遗传关系分析

基于SSR标记的'黑果枸杞'F1代群体杂种鉴定及遗传关系分析

扫码查看
开展基于SSR标记的'黑果枸杞'F1 代群体杂种鉴定及遗传关系分析,为其遗传图谱构建、基因QTL定位以及高花色苷含量新品种选育提供理论支撑。以'黑果枸杞'与'白果枸杞'杂交F1 代群体('Lr-GA'与'Lr-GB')为材料,利用11对高多态性SSR引物进行F1 代真实性鉴定,并进行遗传多样性与遗传相似性系数分析。11对SSR引物在正反交2个F1 代群体中扩增到10株异常基因型单株,鉴定为假杂种,其余397株为真杂种,真杂种率为96。81%;卡方检验发现仅有1个位点出现偏离(ML0116,P<0。050),其余10个位点均符合孟德尔分离定律。在正反交2个群体中,11对SSR标记分别检测到64个和48个等位基因位点,每个标记等位基因数(Na)在2~9,有效等位基因数(Ne)的变化范围为1。55~4。35,Shannon's信息指数(I)的变化范围在0。58~1。53,观测杂合度(Ho)的变化范围在0。45~1。00,期望杂合度(He)的变化范围在0。35~0。77,F检验值的变化范围在-0。58~0。22;基因多态性信息含量(PIC)的变化范围在0。30~0。73,平均值为0。59,LM0069和LM0101的多态性适中(0。25<PIC<0。5),其他标记多态性较高,检测能力较强(PIC>0。5)。基于Nei's遗传距离,UPGMA法聚类结果显示,在Nei's遗传距离0。214处,'Lr-GA'群体分为 2组,'黑果枸杞'为组Ⅰ,'白果枸杞'和293株F1 代单株聚为组Ⅱ。在Nei's遗传距离0。29处,'Lr-GB'群体分为 2组,'黑果枸杞'为组Ⅰ,'白果枸杞'和101株F1 代单株聚为组Ⅱ。总体来看,子代经杂交后,多数SSR位点发生了变异,与父本比较而言,其遗传物质更多来源于母本。采用SSR分子标记法可对'黑果枸杞'的杂交F1 代群体进行有效的杂种鉴定,杂交F1 代单株的基因分离比符合孟德尔分离定律,且与母本有较近的遗传关系。
SSR-Based Hybrid Identification and Genetic Relationship Analysis of F1 Hybrid Progenies of Lycium ruthenicum
The objective of this study was to identify and analyze the genetic relationship of F1 hybrid based on SSR markers to provide theoretical support for the construction of genetic map,QTL mapping,and the breeding of new cultivars with high anthocyanin content.Taking F1 population'Lr-GA'and'Lr-GB'derived from Lycium ruthenicum and L.ruthenicum'Baiguo'as materials,11 highly polymorphic SSR primer pairs were used to identify the authenticity of F1.Genetic diversity and similarity coefficient were then analyzed.A total of 10 abnormal genotype plants were amplified in 2 F1 progenies using 11 pairs of SSR primers,and identified as false hybrids.The remaining 397 progenies were proved to be real hybrids,the real hybrid rate was 96.81%.Chi-square test revealed only one deviated locus(ML0116,P<0.050),the remaining 10 loci were in accordance with Mendel's law of segregation.In the two hybrids of reciprocal crosses,64 and 48 alleles were detected by 11 pairs of SSR markers,respectively.The number of alleles per marker(Na)ranged from 2 to 9,the effective number of alleles(Ne)ranged from 1.55 to 4.35,the range of Shannon's information index(I)was 0.58 to 1.53,the observed heterozygosity(Ho)ranged from 0.45 to 1.00,the expected heterozygosity(He)ranged from 0.35 to 0.77,and the range of F-test values was-0.58 to 0.22.The range of gene polymorphism information content(PIC)was 0.30 to 0.73,with an average value of 0.59.LM0069 and LM0101 has moderate polymorphisms(0.25<PIC<0.5),while other markers were high and with strong detection ability(PIC>0.5).According to the result of UPGMA clustering,the'Lr-GA'progenies was divided into two groups at the Nei's genetic distance of 0.214,'L.ruthenicum'was Group I and'L.ruthenicum'Baiguo'and 293 F1 individuals were clustered in GroupⅡ.'Lr-GB'population was divided into two groups at Nei's genetic distance of 0.29,'L.ruthenicum'was Group I and'L.ruthenicum'Baiguo'and 101 F1 individuals clustered in Group Ⅱ.Overall,most SSR loci of progenies were variant after hybridization,and the more genetic information derived from the maternal plants than paternal plants.The SSR molecular marker method can identify the F1 hybrids of'L.rutheni-cum'effectively.The genetic separation ratio of F1 hybrids complies with Mendel's law of segregation,and they have close genetic relationship with maternal parent.

Lycium ruthenicumSSR markerhybrid identificationgenetic diversitygenetic relationship

戴国礼、张波、米佳、尹跃、秦垦、何昕孺

展开 >

宁夏农林科学院 枸杞科学研究所/国家枸杞工程技术研究中心,宁夏 银川 750002

黑果枸杞 SSR 杂种鉴定 遗传多样性 遗传关系

2025

西北林学院学报
西北农林科技大学

西北林学院学报

北大核心
影响因子:1.078
ISSN:1001-7461
年,卷(期):2025.40(1)