ICAR-Central Agroforestry Research Institute, Jhansi, India.
Chaudhary Charan Singh Haryana Agricultural University, Hisar, Haryana, India.
Int J Radiat Biol. 2022;98(1):69-81. doi: 10.1080/09553002.2022.1998710. Epub 2021 Nov 12.
Mungbean yellow mosaic India virus (MYMIV) is a serious constraint in the mungbean which is a potential source of easily digestible high-quality proteins, fibers, minerals, and vitamins in Asian countries. Developing resistant cultivars is the most cost-effective, eco-friendly, and sustainable approach to protect mungbean from MYMIV damage. Mutation breeding provides a quick and cost-effective way of developing resistance as lack of genetic variability is the biggest bottleneck for other traditional breeding tools.
Outstanding but MYMIV-sensitive varieties of mungbean, viz., MH 2-15 and MH 318 were mutagenized through various individual and combined doses of gamma-rays and Ethyl methanesulfonate (EMS) and evaluated in M and M generations for the appearance of resistance reactions. This was subsequently validated through marker-assisted genotyping using previously reported Yellow Mosaic Disease (YMD) linked markers.
The phenotyping in M generation yielded 64 MYMIV resistant mutants whereas, marker-assisted genotyping identified the 22 mutants with true resistance. Markers YR4, CYR1, and CEDG180 were found associated with MYMIV resistance whereas, DMB-SSR158 did not show any amplification. Among identified resistant mutants, ten lines exhibited at par and two revealed a little higher seed yield over controls.
The mutagenesis created significant variability in MYMIV resistance as well as seed yield per plant. YR4, CYR1, and CEDG180 are found to be linked with the MYMIV loci in the mungbean and could be utilized for MYMIV resistance breeding. Mutant M-37 from MH 2-15 and M-104 from MH 318 exhibited more seed yield along with MYMIV resistance which upon further validation can be released as a variety. The induced mutagenesis integrated with powerful emerging molecular and next-generation sequencing (NGS) tools would be highly helpful in breeding mungbean for durable resistance against threatening MYMIV.
绿豆黄花叶病毒(MYMIV)是绿豆的严重限制因素,绿豆是亚洲国家容易消化的高质量蛋白质、纤维、矿物质和维生素的潜在来源。培育抗性品种是保护绿豆免受 MYMIV 损害最具成本效益、环保和可持续的方法。诱变育种为开发抗性提供了一种快速且具有成本效益的方法,因为缺乏遗传变异性是其他传统育种工具的最大瓶颈。
对敏感但表现出色的绿豆品种 MH 2-15 和 MH 318 进行不同剂量的γ射线和乙基甲磺酸(EMS)诱变处理,并在 M 和 M 世代中评估其抗性反应的出现。随后通过使用先前报道的黄花叶病(YMD)连锁标记的标记辅助基因型鉴定进行验证。
在 M 代中表型鉴定出 64 个 MYMIV 抗性突变体,而标记辅助基因型鉴定出 22 个具有真正抗性的突变体。标记 YR4、CYR1 和 CEDG180 与 MYMIV 抗性相关,而 DMB-SSR158 没有扩增。在鉴定出的抗性突变体中,有 10 个系表现相当,有 2 个系的种子产量略高于对照。
诱变在 MYMIV 抗性和每株植物的种子产量方面产生了显著的变异性。在绿豆中发现 YR4、CYR1 和 CEDG180 与 MYMIV 位点连锁,可用于 MYMIV 抗性育种。MH 2-15 的 M-37 突变体和 MH 318 的 M-104 突变体表现出更高的种子产量和 MYMIV 抗性,进一步验证后可作为品种释放。将诱导诱变与强大的新兴分子和下一代测序(NGS)工具相结合,将极大地有助于培育对威胁性 MYMIV 具有持久抗性的绿豆。