Division of Plant Pathology, ICAR Indian Agricultural Research Institute, New Delhi, 110012, India.
Division of Genetics, ICAR Indian Agricultural Research Institute, New Delhi, 110012, India.
Planta. 2024 May 4;259(6):143. doi: 10.1007/s00425-024-04413-2.
The investigation is the first report on genome-wide identification and characterization of NBLRR genes in pearl millet. We have shown the role of gene loss and purifying selection in the divergence of NBLRRs in Poaceae lineage and candidate CaNBLRR genes for resistance to Magnaporthe grisea infection. Plants have evolved multiple integral mechanisms to counteract the pathogens' infection, among which plant immunity through NBLRR (nucleotide-binding site, leucine-rich repeat) genes is at the forefront. The genome-wide mining in pearl millet (Cenchrus americanus (L.) Morrone) revealed 146 CaNBLRRs. The variation in the branch length of NBLRRs showed the dynamic nature of NBLRRs in response to evolving pathogen races. The orthology of NBLRRs showed a predominance of many-to-one orthologs, indicating the divergence of NBLRRs in the pearl millet lineage mainly through gene loss events followed by gene gain through single-copy duplications. Further, the purifying selection (Ka/Ks < 1) shaped the expansion of NBLRRs within the lineage of pear millet and other members of Poaceae. Presence of cis-acting elements, viz. TCA element, G-box, MYB, SARE, ABRE and conserved motifs annotated with P-loop, kinase 2, RNBS-A, RNBS-D, GLPL, MHD, Rx-CC and LRR suggests their putative role in disease resistance and stress regulation. The qRT-PCR analysis in pearl millet lines showing contrasting responses to Magnaporthe grisea infection identified CaNBLRR20, CaNBLRR33, CaNBLRR46 CaNBLRR51, CaNBLRR78 and CaNBLRR146 as putative candidates. Molecular docking showed the involvement of three and two amino acid residues of LRR domains forming hydrogen bonds (histidine, arginine and threonine) and salt bridges (arginine and lysine) with effectors. Whereas 14 and 20 amino acid residues of CaNBLRR78 and CaNBLRR20 showed hydrophobic interactions with 11 and 9 amino acid residues of effectors, Mg.00g064570.m01 and Mg.00g006570.m01, respectively. The present investigation gives a comprehensive overview of CaNBLRRs and paves the foundation for their utility in pearl millet resistance breeding through understanding of host-pathogen interactions.
该研究首次报道了在黍属植物中全基因组鉴定和特征化 NBLRR 基因。我们展示了基因丢失和纯化选择在禾本科 NBLRR 分化中的作用,以及候选 CaNBLRR 基因对稻瘟病菌感染的抗性。植物已经进化出多种综合机制来抵抗病原体的感染,其中通过 NBLRR(核苷酸结合位点,富含亮氨酸重复)基因的植物免疫处于前沿。在珍珠 millet(Cenchrus americanus (L.) Morrone)中的全基因组挖掘揭示了 146 个 CaNBLRR。NBLRR 分支长度的变化表明 NBLRR 对进化的病原体种群的动态响应。NBLRR 的同源性显示出许多到一个的直系同源物占优势,表明 NBLRR 在珍珠 millet 谱系中的分化主要是通过基因丢失事件,然后通过单拷贝重复获得基因。此外,纯化选择(Ka/Ks<1)塑造了 NBLRR 在黍属和禾本科其他成员中的扩展。顺式作用元件(如 TCA 元件、G 框、MYB、SARE、ABRE 和注释为 P-loop、激酶 2、RNBS-A、RNBS-D、GLPL、MHD、Rx-CC 和 LRR 的保守基序)的存在表明它们在疾病抗性和应激调节中的潜在作用。在对稻瘟病菌感染表现出不同反应的珍珠 millet 品系中的 qRT-PCR 分析鉴定了 CaNBLRR20、CaNBLRR33、CaNBLRR46、CaNBLRR51、CaNBLRR78 和 CaNBLRR146 为潜在候选基因。分子对接显示 LRR 结构域的三个和两个氨基酸残基(组氨酸、精氨酸和苏氨酸)以及盐桥(精氨酸和赖氨酸)与效应物形成氢键和盐桥。而 CaNBLRR78 和 CaNBLRR20 的 14 个和 20 个氨基酸残基与效应物的 11 个和 9 个氨基酸残基分别表现出疏水性相互作用,Mg.00g064570.m01 和 Mg.00g006570.m01。本研究全面概述了 CaNBLRR,并通过了解宿主-病原体相互作用,为其在珍珠 millet 抗性育种中的应用奠定了基础。