Efficient isolated microspore culture protocol for callus induction and plantlet regeneration in japonica rice (Oryza sativa L.).

IF 4.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Plant Methods Pub Date : 2024-05-24 DOI:10.1186/s13007-024-01189-0
Runhong Gao, Yingjie Zong, Shuwei Zhang, Guimei Guo, Wenqi Zhang, Zhiwei Chen, Ruiju Lu, Chenghong Liu, Yifei Wang, Yingbo Li
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Abstract

Background: Isolated microspore culture is a useful biotechnological technique applied in modern plant breeding programs as it can produce doubled haploid (DH) plants and accelerate the development of new varieties. Furthermore, as a single-cell culture technique, the isolated microspore culture provides an excellent platform for studying microspore embryogenesis. However, the reports on isolated microspore culture are rather limited in rice due to the low callus induction rate, poor regeneration capability, and high genotypic dependency. The present study developed an effective isolated microspore culture protocol for high-frequency androgenesis in four japonica rice genotypes. Several factors affecting the isolated microspore culture were studied to evaluate their effects on callus induction and plantlet regeneration.

Results: Low-temperature pre-treatment at 4 ℃ for 10-15 days could effectively promote microspore embryogenesis in japonica rice. A simple and efficient method was proposed for identifying the microspore developmental stage. The anthers in yellow-green florets located on the second type of primary branch on the rice panicle were found to be the optimal stage for isolated microspore culture. The most effective induction media for callus induction were IM2 and IM3, depending on the genotype. The optimal concentration of 2, 4-D in the medium for callus induction was 1 mg/L. Callus induction was negatively affected by a high concentration of KT over 1.5 mg/L. The differentiation medium suitable for japonica rice microspore callus comprised 1/2 MS, 2 mg/L 6-BA, 0.5 mg/L NAA, 30 g/L sucrose, and 6 g/L agar. The regeneration frequency of the four genotypes ranged from 61-211 green plantlets per 100 mg calli, with Chongxiangjing showing the highest regeneration frequency.

Conclusions: This study presented an efficient protocol for improved callus induction and green plantlet regeneration in japonica rice via isolated microspore culture, which could provide valuable support for rice breeding and genetic research.

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用于粳稻(Oryza sativa L.)胼胝体诱导和小植株再生的高效分离小孢子培养方案。
背景:分离小孢子培养是现代植物育种计划中一项有用的生物技术,因为它可以培育出双倍单倍体(DH)植株,加速新品种的开发。此外,作为一种单细胞培养技术,离体小孢子培养为研究小孢子胚胎发生提供了一个极好的平台。然而,由于胼胝体诱导率低、再生能力差、基因型依赖性强等原因,有关水稻分离小孢子培养的报道相当有限。本研究开发了一种有效的分离小孢子培养方案,用于四种粳稻基因型的高频雄性发生。研究了影响分离小孢子培养的几个因素,以评估它们对胼胝体诱导和小植株再生的影响:结果:4 ℃低温预处理 10-15 天可有效促进粳稻小孢子胚胎发生。提出了一种简单有效的小孢子发育阶段鉴定方法。结果发现,位于水稻圆锥花序第二类主枝上的黄绿色小花的花药是分离小孢子培养的最佳阶段。根据基因型的不同,诱导胼胝体最有效的诱导培养基是 IM2 和 IM3。培养基中 2,4-D 诱导胼胝体的最佳浓度为 1 毫克/升。KT 浓度超过 1.5 mg/L 会对胼胝体诱导产生不利影响。适合粳稻小孢子胼胝体的分化培养基包括 1/2 MS、2 mg/L 6-BA、0.5 mg/L NAA、30 g/L 蔗糖和 6 g/L 琼脂。四个基因型每 100 毫克胼胝体的再生频率在 61-211 个绿色小植株之间,其中崇香晶的再生频率最高:本研究提出了一种通过分离小孢子培养提高粳稻胼胝体诱导和绿色小植株再生的有效方法,可为水稻育种和遗传研究提供有价值的支持。
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来源期刊
Plant Methods
Plant Methods 生物-植物科学
CiteScore
9.20
自引率
3.90%
发文量
121
审稿时长
2 months
期刊介绍: Plant Methods is an open access, peer-reviewed, online journal for the plant research community that encompasses all aspects of technological innovation in the plant sciences. There is no doubt that we have entered an exciting new era in plant biology. The completion of the Arabidopsis genome sequence, and the rapid progress being made in other plant genomics projects are providing unparalleled opportunities for progress in all areas of plant science. Nevertheless, enormous challenges lie ahead if we are to understand the function of every gene in the genome, and how the individual parts work together to make the whole organism. Achieving these goals will require an unprecedented collaborative effort, combining high-throughput, system-wide technologies with more focused approaches that integrate traditional disciplines such as cell biology, biochemistry and molecular genetics. Technological innovation is probably the most important catalyst for progress in any scientific discipline. Plant Methods’ goal is to stimulate the development and adoption of new and improved techniques and research tools and, where appropriate, to promote consistency of methodologies for better integration of data from different laboratories.
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