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中国农学通报

中国农学通报 ›› 2022, Vol. 38 ›› Issue (30): 35-40.doi: 10.11924/j.issn.1000-6850.casb2021-1062

所属专题： 生物技术； 园艺

• 农学·农业基础科学 • 上一篇    下一篇

不同甜菜单胚细胞质雄性不育系与保持系的遗传多样性分析

赵雅儒1,2(), 邳植1,2, 刘蕊3, 马语嫣1,2, 吴则东1,2()   

  1. 1黑龙江大学现代农业与生态环境学院,哈尔滨 150080
    2黑龙江省普通高校甜菜遗传育种重点实验室/黑龙江大学,哈尔滨 150080
    3黑龙江省种业技术服务中心,哈尔滨,150080
  • 收稿日期:2021-11-05 修回日期:2022-03-23 出版日期:2022-10-25 发布日期:2022-10-27
  • 通讯作者: 吴则东
  • 作者简介:赵雅儒,女,1998年出生,宁夏吴忠人,硕士研究生,主要从事甜菜遗传及分子育种研究。通信地址：150080 黑龙江省哈尔滨市南岗区学府路74号 黑龙江大学现代农业与生态环境学院,E-mail： 931178094@qq.com。
  • 基金资助:
    财政部和农业农村部：国家现代农业产业技术体系资助(CARS-170111);黑龙江大学研究生创新科研项目资助(YJSCX2021-220HLJU)

Genetic Diversity Analysis of Monogerm Cytoplasmic Male Sterile Lines and Maintainer Lines of Sugar Beet

ZHAO Yaru1,2(), PI Zhi1,2, LIU Rui3, MA Yuyan1,2, WU Zedong1,2()   

  1. 1College of Advanced Agriculture and Ecological Environment, Heilongjiang University, Harbin 150080
    2Key Laboratory of Sugar Beet Genetic Breeding/Heilongjiang University, Harbin 150080
    3Heilongjiang Seed Industry Technical Service Center, Harbin 150080
  • Received:2021-11-05 Revised:2022-03-23 Online:2022-10-25 Published:2022-10-27
  • Contact: WU Zedong

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摘要：

利用35对SSR引物分析40对不同的甜菜单胚细胞质雄性不育系与保持系的遗传多样性。结果表明：每对引物扩增得到的条带数在2~12之间,有效等位基因数(Ne)、Shannon’s信息指数(I)、Nei’s基因多样性指数(H)的平均值分别为2.306、0.891和0.519。采用类平均法(UPGMA)进行聚类分析并计算遗传距离。聚类结果显示,除供试材料22与其他材料的遗传距离较大,亲缘关系较远,单独为一类群;其余的供试甜菜品系可分为4个类群;共有14对甜菜单胚细胞质雄性不育系与保持系完全聚合在一起,说明经过回交后,不育系和保持系的细胞核基因组之间几乎达到一致,纯度较高,今后可以直接应用于甜菜育种中;另有26对纯度较低,遗传距离较大,还需要继续进行回交至纯合。80份供试材料的遗传距离最大为0.462,最小为0.120。14对聚合在一起的原配组中的不育系之间遗传距离各不相同,今后可选择14对中遗传距离较大的不育系和其异型保持系配制二元不育系,用于杂交种中的母本。加大培育出甜菜新品种的可能性,同时减少了育种工作中的盲目性,有效的提高了甜菜育种效率。

关键词: 甜菜, SSR分子标记, 细胞质雄性不育系, 遗传多样性

Abstract:

35 pairs of SSR primers were used to analyze the genetic diversity of 40 pairs of monogerm cytoplasmic male sterile lines and maintainer lines of sugar beet. The results showed that: the number of bands amplified by each pair of primers ranged from 2 and 12, and the average value of effective number of alleles (Ne), Shannon’s information index (I) and Nei’s gene diversity index (H) was 2.306, 0.891 and 0.519 respectively. The UPGMA method was used for cluster analysis and genetic distance calculation. The cluster analysis results showed that tested material 22 had a far genetic distance from other materials, which indicated a distant genetic relationship, and the material belonged to a separate group. The rest of the tested sugar beet lines could be divided into four groups. A total of 14 pairs of monogerm cytoplasmic male sterile lines and maintainer lines of sugar beet were completely polymerized together, indicating that after backcrossing, the nuclear genomes of male sterile lines and maintainer lines were almost identical with high purity, which could be directly used in sugar beet breeding in the future. The other 26 pairs of low purity, large genetic distance, still need to continue to backcross to homozygous. The maximum genetic distance of the 80 tested materials was 0.462 and the minimum was 0.120. The genetic distances of the sterile lines in the 14 pairs of primary mating groups were different. In the future, sugar beet cytoplasmic male sterile lines with large genetic distance from the 14 pairs could be selected with their heterogeneous maintainer lines to prepare binary male sterile lines for female parents in hybrids. The study can promote new sugar beet variety breeding and effectively improve the breeding efficiency.

Key words: sugar beet, SSR molecular marker, cytoplasmic male sterile line, genetic diversity

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