MsmiR171 targets <i>MsSCL6</i> to mediate selenium-regulated chlorophyll biosynthesis in alfalfa

Alfalfa (<i>Medicago sativa</i> L.) is a globally pivotal legume forage. Selenium (Se), an essential trace element for humans and animals, can significantly enhance the growth and development of alfalfa. Chlorophyll is the central pigment of plant photosynthesis. Previous research on chlorophyll synthesis in alfalfa has mainly focused on transcriptional regulation, environmental factors (light, nutrient availability), and phytohormone signaling, while fewer studies have been conducted at the post-transcriptional level. Through whole transcriptome sequencing analysis, microRNAs (miRNAs) were identified as positively responsive to Se. This study focused on the regulation of chlorophyll synthesis by the miR171-<i>SCL6</i> module in alfalfa. β-glucuronidase staining and dual-luciferase assays revealed that MsmiR171 negatively regulated the transcript levels of the <i>SCARECROW-LIKE 6</i> transcription factor <i>MsSCL6.</i> Subcellular localization analysis revealed that MsSCL6 was mainly in the cell nucleus. Functional analyses demonstrated that MsmiR171 promoted chlorophyll synthesis and photosynthesis in alfalfa, while <i>MsSCL6</i> negatively regulated chlorophyll synthesis. Notably, Se treatment upregulated MsmiR171 expression, downregulated <i>MsSCL6</i> expression<i>,</i> and enhanced chlorophyll accumulation. qRT-PCR analysis revealed differential expression of <i>MsPOR</i> in MsmiR171 and <i>MsSCL6</i> overexpression or silencing plants. Combined yeast one-hybrid and dual-luciferase assays demonstrated that MsSCL6 transcriptionally represses <i>MsPOR</i> through direct promoter binding, suppressing chlorophyll accumulation. In summary, this study for the first time revealed the mechanism of the MsmiR171-<i>MsSCL6</i>-<i>MsPOR</i> module mediating Se-regulated chlorophyll biosynthesis in alfalfa. These findings provide a theoretical foundation and technical guidance for alfalfa breeding and the production of Se-enriched forage.

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Publication Details

Journal
Horticulture Research
Published
2025-11-12
DOI
https://doi.org/10.1093/hr/uhaf305
Primary Topic
Photosynthetic Processes and Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

MsmiR171 targets MsSCL6 to mediate selenium-regulated chlorophyll biosynthesis in alfalfa

Yuhua Shi, Shilong Su, Mengli Xu, Yonggui Ma et al.
Horticulture Research
Photosynthetic Processes and Mechanisms
article

MsmiR171 targets MsSCL6 to mediate selenium-regulated chlorophyll biosynthesis in alfalfa

Yuhua Shi, Shilong Su, Mengli Xu, Yonggui Ma, Yu Sheng, Qingdong Wang, Baohong Tang
article en

Abstract

Alfalfa (<i>Medicago sativa</i> L.) is a globally pivotal legume forage. Selenium (Se), an essential trace element for humans and animals, can significantly enhance the growth and development of alfalfa. Chlorophyll is the central pigment of plant photosynthesis. Previous research on chlorophyll synthesis in alfalfa has mainly focused on transcriptional regulation, environmental factors (light, nutrient availability), and phytohormone signaling, while fewer studies have been conducted at the post-transcriptional level. Through whole transcriptome sequencing analysis, microRNAs (miRNAs) were identified as positively responsive to Se. This study focused on the regulation of chlorophyll synthesis by the miR171-<i>SCL6</i> module in alfalfa. β-glucuronidase staining and dual-luciferase assays revealed that MsmiR171 negatively regulated the transcript levels of the <i>SCARECROW-LIKE 6</i> transcription factor <i>MsSCL6.</i> Subcellular localization analysis revealed that MsSCL6 was mainly in the cell nucleus. Functional analyses demonstrated that MsmiR171 promoted chlorophyll synthesis and photosynthesis in alfalfa, while <i>MsSCL6</i> negatively regulated chlorophyll synthesis. Notably, Se treatment upregulated MsmiR171 expression, downregulated <i>MsSCL6</i> expression<i>,</i> and enhanced chlorophyll accumulation. qRT-PCR analysis revealed differential expression of <i>MsPOR</i> in MsmiR171 and <i>MsSCL6</i> overexpression or silencing plants. Combined yeast one-hybrid and dual-luciferase assays demonstrated that MsSCL6 transcriptionally represses <i>MsPOR</i> through direct promoter binding, suppressing chlorophyll accumulation. In summary, this study for the first time revealed the mechanism of the MsmiR171-<i>MsSCL6</i>-<i>MsPOR</i> module mediating Se-regulated chlorophyll biosynthesis in alfalfa. These findings provide a theoretical foundation and technical guidance for alfalfa breeding and the production of Se-enriched forage.

Horticulture ResearchVol. 13(2)
Qinghai Normal University (CN), Zhengzhou University (CN), First Affiliated Hospital of Henan University (CN)
National Natural Science Foundation of China, China Agricultural University, Tsinghua University, Special Fund for Agro-scientific Research in the Public Interest
Openalex Percentile: Top 70%
Photosynthetic Processes and Mechanisms
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