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大豆丙酮酸激酶基因家族的特征分析及一个可能的盐响应基因 GmPK21 的鉴定。

Characterization of the pyruvate kinase gene family in soybean and identification of a putative salt responsive gene GmPK21.

机构信息

Crop Research Institute, Shandong Academy of Agricultural Sciences, 202 Gongye North Road, Jinan, 250100, Shandong, China.

Shandong Engineering Laboratory of Featured Crops, 202 Gongye North Road, Jinan, 250100, Shandong, China.

出版信息

BMC Genomics. 2024 Jan 22;25(1):88. doi: 10.1186/s12864-023-09929-7.

Abstract

BACKGROUND

As a key regulatory enzyme in the glycolysis pathway, pyruvate kinase (PK) plays crucial roles in multiple physiological processes during plant growth and is also involved in the abiotic stress response. However, little information is known about PKs in soybean.

RESULTS

In this study, we identified 27 PK family genes against the genome of soybean cultivar Zhonghuang13. They were classified into 2 subfamilies including PKc and PKp. 22 segmental duplicated gene pairs and 1 tandem duplicated gene pair were identified and all of them experienced a strong purifying selective pressure during evolution. Furthermore, the abiotic stresses (especially salt stress) and hormone responsive cis-elements were present in the promoters of GmPK genes, suggesting their potential roles in abiotic stress tolerance. By performing the qRT-PCR, 6 GmPK genes that continuously respond to both NaCl and ABA were identified. Subsequently, GmPK21, which represented the most significant change under NaCl treatment was chosen for further study. Its encoded protein GmPK21 was localized in the cytoplasm and plasma membrane. The transgenic Arabidopsis overexpressing GmPK21 exhibited weakened salinity tolerance.

CONCLUSIONS

This study provides genomic information of soybean PK genes and a molecular basis for mining salt tolerance function of PKs in the future.

摘要

背景

丙酮酸激酶(PK)作为糖酵解途径中的关键调节酶,在植物生长过程中的多个生理过程中发挥着重要作用,并且还参与非生物胁迫响应。然而,关于大豆中的 PK 知之甚少。

结果

本研究针对大豆品种中黄 13 的基因组,鉴定了 27 个 PK 家族基因。它们被分为 2 个子家族,包括 PKc 和 PKp。鉴定到 22 个片段重复基因对和 1 个串联重复基因对,它们在进化过程中都经历了强烈的纯化选择压力。此外,GmPK 基因启动子中存在非生物胁迫(尤其是盐胁迫)和激素响应顺式元件,表明它们在非生物胁迫耐受中可能发挥作用。通过进行 qRT-PCR,鉴定到 6 个对 NaCl 和 ABA 均持续响应的 GmPK 基因。随后,选择 NaCl 处理下变化最显著的 GmPK21 进行进一步研究。其编码的 GmPK21 蛋白定位于细胞质和质膜中。过表达 GmPK21 的转基因拟南芥表现出较弱的耐盐性。

结论

本研究提供了大豆 PK 基因的基因组信息,为未来挖掘 PK 耐盐功能提供了分子基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7d/10802038/14e0cf177d7d/12864_2023_9929_Fig1_HTML.jpg

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