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大豆GmALMT基因家族在大豆适应低磷胁迫中的功能研究

haracterization of the GmALMT gene family in soybean responsive to Pi starvation

中文摘要英文摘要

低磷胁迫是酸性土壤上限制作物生产的重要因子。由ALMT基因家族介导的苹果酸分泌具有提高难溶磷(P)利用率的潜在功能。本研究发现,大豆基因组中共有34个GmALMT成员,进化树分析表明它们来自两个不同的分支。其中,有26个GmALMT基因在大豆叶、根及花的表达受外界磷有效性的影响。对根部受磷饥饿特异增强表达的基因,GmALMT5,进行功能研究。结果显示,GmALMT5定位于细胞质膜上,并参与介导根系苹果酸的外排。当以难溶磷Ca-P作为唯一磷源时,超量表达GmALMT5能够促进拟南芥生长并显著增加拟南芥中磷含量。以上结果表明,大豆GmALMT家族在大豆磷营养中具有多样化的功能,而GmALMT5可能参与了大豆在低磷条件下对外部难溶磷的利用。

Phosphorus (P) deficiency is a major factor limiting crop production. A potential mechanism to enhance utilization of sparingly soluble forms of this sparsely available element is the secretion of organic acids, such as malate from roots. Malate exudation is mainly mediated by the ALMT family in plants. In this study, a total of 34 GmALMT genes were identified in the soybean genome, with two distinct clades detected in the phylogenetic tree. Expression patterns diverged considerably among GmALMT genes in response to Pi starvation in leaves, roots and flowers, with expression altered by P availability in 26 of the 34 GmALMTs. One root specific member with expression enhanced by Pi-starvation, GmALMT5, was chosen for dissecting the role of ALMT in controlling malate exudation. Results showed that GmALMT5 is a root cell plasma membrane channel protein that mediates malate efflux. Furthermore, it was found that both growth and P concentration of transgenic Arabidopsis lines with GmALMT5 overexpression were significantly increased when sparingly soluble Ca-P was applied as the sole external P source. Taken together, these results suggest that soybean GmALMT proteins have diverse functions in P nutrition. Closer inspection revealed that one member, GmALMT5, might contribute to the utilization of sparingly soluble extracellular sources of P by soybean under P limited conditions

梁翠月、吴炜炜

农业科学研究植物学生理学

植物营养大豆苹果酸转运子磷。

Plant NutritionSoybeanMalate TransportersPhosphorus.

梁翠月,吴炜炜.大豆GmALMT基因家族在大豆适应低磷胁迫中的功能研究[EB/OL].(2017-12-04)[2025-08-04].http://www.paper.edu.cn/releasepaper/content/201712-43.点此复制

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