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通过快中子辐照结合离体培养产生花生突变体。

Generation of peanut mutants by fast neutron irradiation combined with in vitro culture.

作者信息

Wang Jing-Shan, Sui Jiong-Ming, Xie Yong-Dun, Guo Hui-Jun, Qiao Li-Xian, Zhao Li-Lan, Yu Shan-Lin, Liu Lu-Xiang

机构信息

College of Life Sciences, Qingdao Agricultural University/Key Lab of Plant Biotechnology in Universities of Shandong Province, Qingdao 266109, China.

Institute of Crop Science, Chinese Academy of Agricultural Sciences/National Key Facility for Crop Gene Resources and Genetic Improvement, National Center of Space Mutagenesis for Crop Improvement, Beijing 100081, China.

出版信息

J Radiat Res. 2015 May;56(3):437-45. doi: 10.1093/jrr/rru121. Epub 2015 Feb 4.

Abstract

Induced mutations have played an important role in the development of new plant varieties. In this study, we investigated the effects of fast neutron irradiation on somatic embryogenesis combined with plant regeneration in embryonic leaflet culture to develop new peanut (Arachis hypogaea L.) germplasm for breeding. The dry seeds of the elite cultivar Luhua 11 were irradiated with fast neutrons at dosages of 9.7, 14.0 and 18.0 Gy. The embryonic leaflets were separated and incubated in a medium with 10.0-mg/l 2,4-D to induce somatic embryogenesis. Next, they were incubated in a medium with 4.0-mg/l BAP for plant regeneration. As the irradiation dosage increased, the frequency of both somatic embryo formation and plantlet regeneration decreased. The regenerated plantlets were grafted onto rootstocks and were transplanted into the field. Later, the mature seeds of the regenerated plants were harvested. The M2 generation plants from most of the regenerated cultivars exhibited variations and segregation in vigor, plant height, branch and pod number, pod size, and pod shape. To determine whether the phenotypes were associated with genomic modification, we compared the DNA polymorphisms between the wild-type plants and 19 M3-generation individuals from different regenerated plants. We used 20 pairs of simple sequence repeat (SSR) primers and detected polymorphisms between most of the mutants and the wild-type plants (Luhua 11). Our results indicate that using a combination of fast neutron irradiation and tissue culture is an effective approach for creating new peanut germplasm.

摘要

诱发突变在新植物品种的培育过程中发挥了重要作用。在本研究中,我们探究了快中子辐照对体细胞胚胎发生的影响,并结合胚小叶培养中的植株再生,以培育用于育种的花生(Arachis hypogaea L.)新种质。选用优良品种鲁花11的干种子,分别用9.7、14.0和18.0 Gy剂量的快中子进行辐照。分离胚小叶并在含有10.0 mg/L 2,4 - D的培养基中培养以诱导体细胞胚胎发生。接下来,将其置于含有4.0 mg/L BAP的培养基中进行植株再生。随着辐照剂量的增加,体细胞胚形成频率和植株再生频率均降低。将再生植株嫁接至砧木上,然后移栽至田间。之后,收获再生植株的成熟种子。大多数再生品种的M2代植株在活力、株高、分枝数、荚果数、荚果大小和荚果形状等方面表现出变异和分离。为确定这些表型是否与基因组修饰相关,我们比较了野生型植株与来自不同再生植株的19个M3代个体之间的DNA多态性。我们使用了20对简单序列重复(SSR)引物,检测到大多数突变体与野生型植株(鲁花11)之间存在多态性。我们的结果表明,结合快中子辐照和组织培养是创建花生新种质的有效方法。

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