Key Laboratory of Germplasm Innovation and Genetic Improvement of Grain and Oil Crops (Co-Construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Crop Breeding and Cultivation Research Institute, Shanghai Academy of Agricultural Sciences, Shanghai 201403, China.
Shanghai Key Laboratory of Agricultural Genetics and Breeding, Shanghai Academy of Agricultural Sciences, Shanghai 201106, China.
Genes (Basel). 2023 Nov 17;14(11):2086. doi: 10.3390/genes14112086.
Anther culture (AC) is a valuable technique in rice breeding. However, the genetic mechanisms underlying anther culturability remain elusive, which has hindered its widespread adoption in rice breeding programs. During AC, microspores carrying favorable alleles for AC are selectively regenerated, leading to segregation distortion (SD) of chromosomal regions linked to these alleles in the doubled haploid (DH) population. Using the AC method, a DH population was generated from the hybrid rice Shenyou 26. A genetic map consisting of 470 SNPs was constructed using this DH population, and SD analysis was performed at both the single- and two-locus levels to dissect the genetic basis underlying anther culturability. Five segregation distortion loci (SDLs) potentially linked to anther culturability were identified. Among these, exhibited an overrepresentation of alleles from the female parent, while , , , and displayed an overrepresentation of alleles from the male parent. Furthermore, six pairs of epistatic interactions (EPIs) that influenced two-locus SDs in the DH population were discovered. A cluster of genetic loci, associated with EPI-1, EPI-3, EPI-4, and EPI-5, overlapped with , indicating that the locus may play a role in regulating anther culturability via both additive and epistatic mechanisms. These findings provide valuable insights into the genetic control of anther culturability in rice and lay the foundation for future research focused on identifying the causal genes associated with anther culturability.
花药培养(Anther Culture,AC)是水稻育种中的一项重要技术。然而,花药培养能力的遗传机制仍难以捉摸,这阻碍了其在水稻育种计划中的广泛应用。在花药培养过程中,携带有利于花药培养的有利等位基因的小孢子被选择性地再生,导致与这些等位基因连锁的染色体区域在加倍单倍体(Doubled Haploid,DH)群体中发生分离失真(Segregation Distortion,SD)。利用 AC 方法,从杂交水稻深优 26 中产生了一个 DH 群体。使用该 DH 群体构建了一个由 470 个 SNP 组成的遗传图谱,并在单基因座和双基因座水平上进行 SD 分析,以剖析与花药培养能力相关的遗传基础。鉴定出了五个潜在与花药培养能力相关的分离失真基因座(Segregation Distortion Loci,SDLs)。其中, 显示出来自母本的等位基因的过度表达,而 、 、 、 则显示出来自父本的等位基因的过度表达。此外,还发现了六个影响 DH 群体中双基因座 SD 的上位性互作(Epistatic Interaction,EPI)对。与 EPI-1、EPI-3、EPI-4 和 EPI-5 相关的遗传基因座簇,与 重叠,表明 基因座可能通过加性和上位性机制在调节花药培养能力方面发挥作用。这些发现为深入了解水稻花药培养能力的遗传控制提供了有价值的见解,并为未来的研究奠定了基础,这些研究将集中在鉴定与花药培养能力相关的因果基因上。