ADP-glucose pyrophosphorylase gene family in soybean and implications in drought stress tolerance
Background ADP-glucose pyrophosphorylase (AGPase) is the key rate-limiting enzyme in starch biosynthesis pathway, and has been identified as a potential target for manipulation strategies aimed at improving crop yield and quality. Objective To identify the AGPase gene family members in soybean, and...
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Veröffentlicht in: | Genes & genomics 2024, 46(10), , pp.1183-1199 |
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Sprache: | eng |
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Zusammenfassung: | Background
ADP-glucose pyrophosphorylase (AGPase) is the key rate-limiting enzyme in starch biosynthesis pathway, and has been identified as a potential target for manipulation strategies aimed at improving crop yield and quality.
Objective
To identify the
AGPase
gene family members in soybean, and explore the potential implications of
GmAGPS2
in drought stress tolerance.
Methods
The genome-wide identification and sequence analysis of soybean
AGPase
gene family was carried out by bioinformatics methods. The
GmAGP
gene expression was analyzed using transcriptome data and quantitative real-time PCR (qRT-PCR). Furthermore, transgenic yeast strains overexpressing
GmAGPS2
were generated, and their growth was observed under drought stress.
Results
In this study, we searched for
AGPase
genes (
GmAGP
) in the soybean genome and identified a total of 14
GmAGP
genes. The GmAGP proteins had a unique conserved NTP_transferase domain and were mainly located in the chloroplast and cytosol. Evolutionarily, the GmAGP proteins can be clustered into two distinct subgroups; within the same subgroup, they displayed a similar distribution pattern of conserved motifs. The
GmAGP
genes exhibited an uneven distribution on 10 chromosomes, and segmental duplication contributed to
AGPase
gene family expansion in soybean. The
GmAGP
genes presented different tissue expression pattern, in which
GmAGPL6
,
GmAGPL9
, and
GmAGPL10
mainly exhibited tissue-specific expression pattern. The promoter of
GmAGP
genes had multiple
cis
-acting elements related to phytohormones and stress responses, and 8
GmAGP
genes contained drought-responsive
cis
-acting elements. qRT‒PCR analysis demonstrated a significant upregulation expression of
GmAGPL6
,
GmAGPL10
, and
GmAGPS2
in response to drought stress. Further functional analysis indicated that
GmAGPS2
gene could improve yeast growth under drought stress conditions and enhance the drought tolerance of yeast.
Conclusion
These results will contribute to further elucidation of the function of
GmAGP
genes, and offer important candidate genes for the genetic improvement of starch and yield-related traits and the breeding of high drought stress tolerance varieties in soybean. |
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ISSN: | 1976-9571 2092-9293 2092-9293 |
DOI: | 10.1007/s13258-024-01558-y |