National Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University/JCIC-MCP, Nanjing, 210095, China.
Zhongshan Biological Breeding Laboratory, Nanjing, 210014, China.
Theor Appl Genet. 2024 Jul 15;137(8):185. doi: 10.1007/s00122-024-04691-0.
Phenotypical, physiological and genetic characterization was carried out on the hybrid necrosis gene from Haynaldia villosa, and the related gene Ne-V was mapped to chromosome arm 2VL. Introducing genetic variation from wild relatives into common wheat through wide crosses is a vital strategy for enriching genetic diversity and promoting wheat breeding. However, hybrid necrosis, a genetic autoimmunity syndrome, often occurs in the offspring of interspecific or intraspecific crosses, restricting both the selection of hybrid parents and the pyramiding of beneficial genes. To utilize the germplasms of Haynaldia villosa (2n = 2x = 14, VV), we conducted wide hybridization between durum wheat (2n = 4x = 28, AABB) and multiple H. villosa accessions to synthesize the amphiploids (2n = 6x = 42, AABBVV). This study revealed that 61.5% of amphiploids derived from the above crosses exhibited hybrid necrosis, with some amphiploids even dying before reaching maturity. However, the initiation time and severity of necrosis varied dramatically among the progenies, suggesting that there were multiple genetic loci or multiple alleles in the same genetic locus conferring to hybrid necrosis in H. villosa accessions. Genetic analysis was performed on the F and derived F populations, which were constructed between amphiploid STH59-1 with normal leaves and amphiploid STH59-2 with necrotic leaves. A semidominant hybrid necrosis-related gene, Ne-V, was mapped to an 11.8-cM genetic interval on the long arm of chromosome 2V, representing a novel genetic locus identified in Triticum-related species. In addition, the hybrid necrosis was correlated with enhanced HO accumulation and cell death, and it was influenced by the temperature and light. Our findings provide a foundation for cloning the Ne-V gene and exploring its molecular mechanism.
对来自节节麦的杂种坏死基因进行了表型、生理和遗传特征分析,相关基因 Ne-V 被定位到 2VL 染色体臂上。通过广泛杂交将野生亲缘种的遗传变异引入普通小麦中,是丰富遗传多样性和促进小麦育种的重要策略。然而,杂种坏死是一种遗传自身免疫综合征,通常发生在种间或种内杂交的后代中,限制了杂种亲本的选择和有益基因的聚合。为了利用节节麦(2n = 2x = 14,VV)的种质资源,我们进行了硬粒小麦(2n = 4x = 28,AABB)与多个节节麦品系的广泛杂交,以合成双二倍体(2n = 6x = 42,AABBVV)。本研究表明,上述杂交产生的 61.5%的双二倍体表现出杂种坏死,有些双二倍体甚至在成熟前死亡。然而,坏死的起始时间和严重程度在后代中差异很大,这表明在节节麦品系中存在多个遗传位点或同一遗传位点中的多个等位基因导致杂种坏死。对具有正常叶片的双二倍体 STH59-1 和具有坏死叶片的双二倍体 STH59-2 之间构建的 F 和衍生 F 群体进行了遗传分析。一个半显性的与杂种坏死相关的基因 Ne-V 被定位到 2V 染色体长臂上 11.8-cM 的遗传区间,代表了在小麦相关物种中鉴定的一个新的遗传位点。此外,杂种坏死与 HO 积累和细胞死亡增强有关,并受温度和光照的影响。我们的研究结果为克隆 Ne-V 基因和探索其分子机制提供了基础。