Si Yaoqi, Lu Qiao, Tian Shuiquan, Niu Jianqing, Cui Man, Liu Xiaolin, Gao Qiang, Shi Xiaoli, Ling Hong-Qing, Zheng Shusong
State Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, the Innovative Academy of Seed Design, Chinese Academy of Sciences, Beijing, 100101, China.
University of Chinese Academy of Sciences, Beijing, 100049, China.
Theor Appl Genet. 2022 Aug;135(8):2665-2673. doi: 10.1007/s00122-022-04140-w. Epub 2022 Jun 22.
A tiller inhibition gene TIN5 was delimited to an approximate 2.1 Mb region on chromosome Tu7 that contains 24 annotated genes. Grain yield in wheat (Triticum aestivum L.) is a polygenic trait representing many developmental processes and their interactions with the environments. Among them, tillering capacity is an important agronomic trait for plant architecture and grain yield, but the genetic basis of tiller formation in wheat remains largely unknown. In this study, we identified a tiller inhibition 5 (tin5) mutant from ethyl methane sulfonate treated G1812 (Triticum urartu Thumanjan ex Gandilyan). A mapping population was constructed with tin5/G3146. Based on the sequence differences between G1812 and G3146, large insertions and deletions (≥ 5 bp) were selected and verified, and a skeleton physical map was constructed with genome-wide 168 polymorphic InDel markers. Genetic analysis revealed that the low-tiller phenotype was controlled by a single recessive locus, which we named TIN5. This locus was mapped to a 2.1-Mb region that contained 24 annotated genes on chromosome Tu7. Among these annotated genes, only TuG1812G0700004539 showed a non-synonymous polymorphism between tin5 and the wild type. Our finding will facilitate its map-based cloning and pave the way for an in-depth analysis of the underlying genetic basis of tiller formation and regulation patterns.
一个分蘖抑制基因TIN5被定位到图7染色体上一个约2.1 Mb的区域,该区域包含24个注释基因。小麦(Triticum aestivum L.)的籽粒产量是一个多基因性状,代表了许多发育过程及其与环境的相互作用。其中,分蘖能力是影响植株形态和籽粒产量的重要农艺性状,但小麦分蘖形成的遗传基础仍 largely unknown。在本研究中,我们从经甲基磺酸乙酯处理的G1812(Triticum urartu Thumanjan ex Gandilyan)中鉴定出一个分蘖抑制5(tin5)突变体。用tin5/G3146构建了一个作图群体。基于G1812和G3146之间的序列差异,选择并验证了大的插入和缺失(≥5 bp),并用全基因组168个多态性InDel标记构建了一个骨架物理图谱。遗传分析表明,低分蘖表型受一个单隐性位点控制,我们将其命名为TIN5。该位点被定位到图7染色体上一个包含24个注释基因的2.1 Mb区域。在这些注释基因中,只有TuG1812G0700004539在tin5和野生型之间表现出非同义多态性。我们的发现将有助于其图位克隆,并为深入分析分蘖形成和调控模式的潜在遗传基础铺平道路。