A novel regulator of wheat tillering LT1 identified by using an upgraded BSA method, uni-BSA.

IF 2.6 3区 农林科学 Q1 AGRONOMY
Molecular Breeding Pub Date : 2024-06-25 eCollection Date: 2024-07-01 DOI:10.1007/s11032-024-01484-7
Yundong Yuan, Bo Lyu, Juan Qi, Xin Liu, Yuanzhi Wang, Pierre Delaplace, Yanfang Du
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Abstract

Branching/tillering is a critical process for plant architecture and grain yield. However, Branching is intricately controlled by both endogenous and environmental factors. The underlying mechanisms of tillering in wheat remain poorly understood. In this study, we identified Less Tiller 1 (LT1) as a novel regulator of wheat tillering using an enhanced bulked segregant analysis (BSA) method, uni-BSA. This method effectively reduces alignment noise caused by the high repetitive sequence content in the wheat genome. Loss-of-function of LT1 results in fewer tillers due to defects in axillary meristem initiation and bud outgrowth. We mapped LT1 to a 6 Mb region on the chromosome 2D short arm and validated a nucleotide-binding (NB) domain encoding gene as LT1 using CRISPR/Cas9. Furthermore, the lower sucrose concentration in the shoot bases of lt1 might result in inadequate bud outgrowth due to disturbances in the sucrose biosynthesis pathways. Co-expression analysis suggests that LT1 controls tillering by regulating TaROX/TaLAX1, the ortholog of the Arabidopsis tiller regulator REGULATOR OF AXILLARY MERISTEM FORMATION (ROX) or the rice axillary meristem regulator LAX PANICLE1 (LAX1). This study not only offers a novel genetic resource for cultivating optimal plant architecture but also underscores the importance of our innovative BSA method. This uni-BSA method enables the swift and precise identification of pivotal genes associated with significant agronomic traits, thereby hastening gene cloning and crop breeding processes in wheat.

Supplementary information: The online version contains supplementary material available at 10.1007/s11032-024-01484-7.

Abstract Image

使用升级版 BSA 方法 uni-BSA 鉴定出小麦分蘖的新型调节因子 LT1。
分枝/分蘖是植物结构和谷物产量的关键过程。然而,分枝受内源和环境因素的复杂控制。人们对小麦分蘖的内在机制仍然知之甚少。在这项研究中,我们利用一种增强的大量分离分析(BSA)方法--uni-BSA--发现了小麦分蘖的新型调控因子少分蘖1(LT1)。这种方法能有效降低小麦基因组中重复序列含量高所造成的配对噪音。LT1功能缺失会导致腋生分生组织起始和芽生长缺陷,从而导致分蘖减少。我们将 LT1 映射到染色体 2D 短臂上的 6 Mb 区域,并利用 CRISPR/Cas9 验证了 LT1 是一个核苷酸结合(NB)结构域编码基因。此外,lt1的芽基部蔗糖浓度较低,可能是由于蔗糖生物合成途径紊乱导致芽生长不足。共表达分析表明,LT1通过调节拟南芥分蘖调节因子REGULATOR OF AXILLARY MERISTEM FORMATION(ROX)或水稻腋生分生组织调节因子LAX PANICLE1(LAX1)的直向异构体TaROX/TaLAX1来控制分蘖。这项研究不仅为培育最佳植物结构提供了一种新的遗传资源,而且还强调了我们创新的 BSA 方法的重要性。这种统一 BSA 方法能迅速准确地鉴定出与重要农艺性状相关的关键基因,从而加快小麦的基因克隆和作物育种进程:在线版本包含补充材料,可查阅 10.1007/s11032-024-01484-7。
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来源期刊
Molecular Breeding
Molecular Breeding 农林科学-农艺学
CiteScore
5.60
自引率
6.50%
发文量
67
审稿时长
1.5 months
期刊介绍: Molecular Breeding is an international journal publishing papers on applications of plant molecular biology, i.e., research most likely leading to practical applications. The practical applications might relate to the Developing as well as the industrialised World and have demonstrable benefits for the seed industry, farmers, processing industry, the environment and the consumer. All papers published should contribute to the understanding and progress of modern plant breeding, encompassing the scientific disciplines of molecular biology, biochemistry, genetics, physiology, pathology, plant breeding, and ecology among others. Molecular Breeding welcomes the following categories of papers: full papers, short communications, papers describing novel methods and review papers. All submission will be subject to peer review ensuring the highest possible scientific quality standards. Molecular Breeding core areas: Molecular Breeding will consider manuscripts describing contemporary methods of molecular genetics and genomic analysis, structural and functional genomics in crops, proteomics and metabolic profiling, abiotic stress and field evaluation of transgenic crops containing particular traits. Manuscripts on marker assisted breeding are also of major interest, in particular novel approaches and new results of marker assisted breeding, QTL cloning, integration of conventional and marker assisted breeding, and QTL studies in crop plants.
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