Ali Ahmad, Zhao Xue-Ting, Lin Ji-Shan, Zhao Ting-Ting, Feng Cui-Lian, Li Ling, Wu Rui-Jie, Huang Qi-Xing, Liu Hong-Bo, Wang Jun-Gang
National Key Laboratory for Tropical Crop Breeding, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, China.
Key Laboratory of Biology and Genetic Resources of Tropical Crops/Key Laboratory for Biology and Genetic Resources of Tropical Crops of Hainan Province, Hainan Institute for Tropical Agricultural Resources, Sanya Institute of Chinese Academy of Tropical Agricultural Sciences, Sanya, 572024, China.
BMC Plant Biol. 2025 Apr 16;25(1):484. doi: 10.1186/s12870-025-06490-1.
The MAP Kinase cascade system is a conserved signaling mechanism essential for plant development, growth, and stress tolerance. Thus far, genes from the MAPK cascade have been identified in several plant species but remain uncharacterized in the polyploid Saccharum spp. Hybrid R570 genome.
This study identified 89 ScMAPK, 24 ScMAPKK, and 107 ScMAPKKK genes through genome-wide analysis. Phylogenetic classification revealed that four subgroups were present in each ScMAPK and ScMAPKK family, and three sub-families (ZIK-like, RAF-like, and MEKK-like) presented in the ScMAPKKK family. Conserved motif and gene structure analysis supported the evolutionary relationships of the three families inferred from the phylogenetic analysis. All of the ScMAPK, ScMAPKK and ScMAPKKK genes were mapped on four scaffolds (Scaffold_88/89/91/92) and nine chromosomes (1-8, 10). Collinearity and gene duplication analysis identified 169 pairs of allelic and non-allelic segmentally duplicated MAPK cascade genes, contributing to their expansion. Additionally, 13 putative 'ss-miRNAs' were predicted to target 87 MAPK cascade genes, with 'ssp-miR168a' alone regulating 45 genes. qRT-PCR analysis revealed differential gene expression under abiotic stressors. ScMAPK07, ScMAPK66, and ScRAF43 were down-regulated and acted as negative regulators. Conversely, ScMAPKK13, ScRAF10, and ScZIK18 were up-regulated at specific time points under drought, with ScZIK18 exhibiting strong defense. Under NaCl stress, most genes were down-regulated, except for slight increases in ScZIK18 and ScMAPKK13, suggesting a positive role in salt stress response. Under CaCl stress, five genes were significantly down-regulated, while ScRAF43 remained unchanged, reflecting their negative roles in stress adaptation and resource conservation.
This study provides insights into MAPK cascade gene evolution and function in sugarcane, highlighting distinct regulatory roles in abiotic stress responses. Interestingly, some genes acted as negative regulators, serving as a mechanism to balance stress responses and prevent overactivation. In contrast, others contributed to defense mechanisms, offering potential targets for stress resilience improvement.
This study contains no clinical trials. Not applicable.
丝裂原活化蛋白激酶(MAPK)级联系统是一种保守的信号传导机制,对植物发育、生长和胁迫耐受性至关重要。到目前为止,已在几种植物物种中鉴定出MAPK级联的基因,但在多倍体甘蔗属杂种R570基因组中仍未得到表征。
本研究通过全基因组分析鉴定出89个甘蔗丝裂原活化蛋白激酶(ScMAPK)、24个丝裂原活化蛋白激酶激酶(ScMAPKK)和107个丝裂原活化蛋白激酶激酶激酶(ScMAPKKK)基因。系统发育分类显示,每个ScMAPK和ScMAPKK家族中存在四个亚组,ScMAPKKK家族中存在三个亚家族(ZIK样、RAF样和MEKK样)。保守基序和基因结构分析支持了系统发育分析推断的三个家族的进化关系。所有ScMAPK、ScMAPKK和ScMAPKKK基因都定位在四个支架(支架_88/89/91/92)和九条染色体(1 - 8、10)上。共线性和基因复制分析确定了169对等位基因和非等位基因片段重复的MAPK级联基因,这促成了它们的扩增。此外,预测有13个假定的“ss - miRNAs”靶向87个MAPK级联基因,仅“ssp - miR168a”就调控45个基因。qRT - PCR分析揭示了非生物胁迫下基因表达的差异。ScMAPK07、ScMAPK66和ScRAF43被下调并作为负调控因子。相反,在干旱条件下,ScMAPKK13、ScRAF10和ScZIK18在特定时间点上调,ScZIK18表现出强大的防御作用。在NaCl胁迫下,除ScZIK18和ScMAPKK13略有增加外,大多数基因被下调,表明它们在盐胁迫反应中起积极作用。在CaCl胁迫下,五个基因显著下调,而ScRAF43保持不变,反映了它们在胁迫适应和资源保护中的负作用。
本研究深入了解了甘蔗中MAPK级联基因的进化和功能,突出了其在非生物胁迫反应中的不同调控作用。有趣的是,一些基因作为负调控因子,作为平衡胁迫反应和防止过度激活的一种机制。相比之下,其他基因有助于防御机制,为提高胁迫恢复力提供了潜在靶点。
本研究不包含临床试验。不适用。