Paper · 2026 · Plant Physiology and Biochemistry

Systematic identification and functional insights into IGT family members involved in leaf angle regulation and abiotic stress response in sugarcane

Ahmad Ali; Rui-Jie Wu; Ji-Shan Lin; et al.

19
claims
39
verbatim quotes
0
citations
3
research areas
✓
Open access · cc-by

Abstract

Sugarcane, a major crop for sugar production, where growth and yield are strongly influenced by plant architecture, particularly leaf angle (LA), and stress adaptation. Optimizing LA improves light capture, photosynthesis, and lodging resistance, regulated by IGT genes, though their role in sugarcane remains unclear. This study identified 50 IGT genes across three Saccharum species: 05 SsIGT in S. spontaneum (AP85-441), 10 SoIGT in S. officinarum (LA-purple), and 35 ScIGT in S. hybrid (XTT22). Phylogenetic analysis classified them into DRO, LAZY, and TAC subfamilies. Promoter analysis revealed cis-regulatory elements linked to stress, hormone responses, and growth regulation, while miRNA prediction indicated post-transcriptional regulation. Protein network analysis highlighted conserved interactions between sugarcane IGT proteins and maize homologs. BR regulates LA and cellular dynamics, shaping sugarcane growth and architecture. Cytological analysis reveals that, moderate brassinosteroids (BRs) (3-5 μM) promoted cell enlargement and increased LA, whereas higher levels (≥10 μM) reduced cell size, restored density, and decreased LA. Subcellular localization shows that ShLAZY1 is predominantly found in the cytoplasm and nucleus, supporting its role as a transcription factor. qRT-PCR revealed that BR treatment significantly upregulated ShDRO2, ShDRO18, ShLAZY1, ShTAC1, and GRAS33, implicating them in leaf joint development and architecture regulation. Under NaCl stress (250 mM), five genes including, ShDRO2, ShDRO18, ShKnox1, ShGn1, and ShGRAS33 functioned as positive regulators, while ShLg1 and ShTAC1 acted as negative regulators, potentially influencing plant architecture via source-sink modulation. These findings highlight the integrated role of IGT genes in LA modulation and stress adaptation, offering strategies for improving sugarcane productivity and resilience.

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Claims 19

Observationobservedoriginal resultmeasured

Claim · model-written summary

Fifty IGT genes were identified across three Saccharum species.

Taxon
SaccharumSaccharume1
Gene
IGT genese1
Outcome
IGT genese1
Value
50e1

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Saccharum
Saccharum · Taxon · picture of the genus (one of its species)Ton Rulkens · CC BY-SA 2.0 · Wikimedia Commons ↗

Verbatim

e1

“This study identified 50 IGT genes across three Saccharum species”

✓ located verbatim in the source · abstract, characters 319–384 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Five SsIGT genes were identified in S. spontaneum (AP85-441).

Taxon
S. spontaneumSaccharum spontaneume2
Material
AP85-441e2
Gene
SsIGTe2
Outcome
SsIGTe2
Value
05e2

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Saccharum spontaneum
Saccharum spontaneum · TaxonScott Bauer · Public domain · Wikimedia Commons ↗

Verbatim

e2

“05 SsIGT in S. spontaneum (AP85-441)”

✓ located verbatim in the source · abstract, characters 386–422 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Ten SoIGT genes were identified in S. officinarum (LA-purple).

Taxon
S. officinarumSaccharum officinarume3
Material
LA-purplee3
Gene
SoIGTe3
Outcome
SoIGTe3
Value
10e3

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Saccharum officinarum
Saccharum officinarum · TaxonTon Rulkens · CC BY-SA 2.0 · Wikimedia Commons ↗

Verbatim

e3

“10 SoIGT in S. officinarum (LA-purple)”

✓ located verbatim in the source · abstract, characters 424–462 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Thirty-five ScIGT genes were identified in S. hybrid (XTT22).

Taxon
S. hybride4
Material
XTT22e4
Gene
ScIGTe4
Outcome
ScIGTe4
Value
35e4

Verbatim

e4

“35 ScIGT in S. hybrid (XTT22)”

✓ located verbatim in the source · abstract, characters 468–497 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Phylogenetic analysis classified the IGT genes into DRO, LAZY and TAC subfamilies.

Taxon
Sugarcanee0
Outcome
DRO, LAZY, and TAC subfamiliese5

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e5

“Phylogenetic analysis classified them into DRO, LAZY, and TAC subfamilies”

✓ located verbatim in the source · abstract, characters 499–572 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Promoter analysis revealed cis-regulatory elements linked to stress, hormone responses and growth regulation.

Taxon
Sugarcanee0
Outcome
cis-regulatory elementse6
Qualifier
linked to stress, hormone responses, and growth regulatione6

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e6

“Promoter analysis revealed cis-regulatory elements linked to stress, hormone responses, and growth regulation”

✓ located verbatim in the source · abstract, characters 574–683 · show in text ↑
Mechanismauthor interpretationoriginal resultmeasured

Claim · model-written summary

A miRNA prediction indicated post-transcriptional regulation in sugarcane IGT genes.

Taxon
Sugarcanee0
Outcome
post-transcriptional regulatione7
Qualifier
miRNA predictione7

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e7

“miRNA prediction indicated post-transcriptional regulation”

✓ located verbatim in the source · abstract, characters 691–749 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Protein network analysis highlighted conserved interactions between sugarcane IGT proteins and maize homologs.

Taxon
sugarcanee1
Gene
IGT proteinse1
Outcome
conserved interactionse1

Verbatim

e1

“Protein network analysis highlighted conserved interactions between sugarcane IGT proteins and maize homologs”

✓ located verbatim in the source · abstract, characters 751–860 · show in text ↑
Intervention effectobservedoriginal resultmeasured

Claim · model-written summary

Moderate BR (3-5 μM) promoted cell enlargement in sugarcane, compared with higher levels (≥10 μM).

Taxon
Sugarcanee0
Treatment
moderate brassinosteroids (BRs) (3-5 μM)e1
Outcome
cell enlargemente1
Direction
promotede1
Comparator
higher levels (≥10 μM)e2

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“moderate brassinosteroids (BRs) (3-5 μM) promoted cell enlargement and increased LA”

✓ located verbatim in the source · abstract, characters 979–1062 · show in text ↑
e2

“whereas higher levels (≥10 μM) reduced cell size, restored density, and decreased LA”

✓ located verbatim in the source · abstract, characters 1064–1148 · show in text ↑
Intervention effectobservedoriginal resultmeasured

Claim · model-written summary

Moderate BR (3-5 μM) increased leaf angle (LA) in sugarcane, compared with higher levels (≥10 μM).

Taxon
Sugarcanee0
Treatment
moderate brassinosteroids (BRs) (3-5 μM)e1
Outcome
LAe1
Direction
increasede1
Comparator
higher levels (≥10 μM)e2

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“moderate brassinosteroids (BRs) (3-5 μM) promoted cell enlargement and increased LA”

✓ located verbatim in the source · abstract, characters 979–1062 · show in text ↑
e2

“whereas higher levels (≥10 μM) reduced cell size, restored density, and decreased LA”

✓ located verbatim in the source · abstract, characters 1064–1148 · show in text ↑
Intervention effectobservedoriginal resultmeasured

Claim · model-written summary

Higher BR levels (≥10 μM) reduced cell size in sugarcane, compared with moderate BR (3-5 μM).

Taxon
Sugarcanee0
Treatment
higher levels (≥10 μM)e2
Outcome
cell sizee2
Direction
reducede2
Comparator
moderate brassinosteroids (BRs) (3-5 μM)e1

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“moderate brassinosteroids (BRs) (3-5 μM) promoted cell enlargement and increased LA”

✓ located verbatim in the source · abstract, characters 979–1062 · show in text ↑
e2

“whereas higher levels (≥10 μM) reduced cell size, restored density, and decreased LA”

✓ located verbatim in the source · abstract, characters 1064–1148 · show in text ↑
Intervention effectobservedoriginal resultmeasured

Claim · model-written summary

Higher BR levels (≥10 μM) decreased leaf angle (LA) in sugarcane, compared with moderate BR (3-5 μM).

Taxon
Sugarcanee0
Treatment
higher levels (≥10 μM)e2
Outcome
LAe2
Direction
decreasede2
Comparator
moderate brassinosteroids (BRs) (3-5 μM)e1

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“moderate brassinosteroids (BRs) (3-5 μM) promoted cell enlargement and increased LA”

✓ located verbatim in the source · abstract, characters 979–1062 · show in text ↑
e2

“whereas higher levels (≥10 μM) reduced cell size, restored density, and decreased LA”

✓ located verbatim in the source · abstract, characters 1064–1148 · show in text ↑
Intervention effectobservedoriginal resultmeasured

Claim · model-written summary

Higher BR levels (≥10 μM) restored cell density in sugarcane, compared with moderate BR (3-5 μM).

Taxon
Sugarcanee0
Treatment
higher levels (≥10 μM)e2
Outcome
densitye2
Direction
restorede2
Comparator
moderate brassinosteroids (BRs) (3-5 μM)e1

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“moderate brassinosteroids (BRs) (3-5 μM) promoted cell enlargement and increased LA”

✓ located verbatim in the source · abstract, characters 979–1062 · show in text ↑
e2

“whereas higher levels (≥10 μM) reduced cell size, restored density, and decreased LA”

✓ located verbatim in the source · abstract, characters 1064–1148 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

ShLAZY1 is predominantly localized to the cytoplasm and nucleus of sugarcane cells.

Taxon
Sugarcanee0
Gene
ShLAZY1e1
Outcome
Subcellular localizatione1
Qualifier
predominantly found in the cytoplasm and nucleuse1

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“Subcellular localization shows that ShLAZY1 is predominantly found in the cytoplasm and nucleus”

✓ located verbatim in the source · abstract, characters 1150–1245 · show in text ↑
Intervention effectobservedoriginal resultsignificant (as stated)measured

Claim · model-written summary

BR treatment significantly upregulated ShDRO2, ShDRO18 and ShLAZY1 in sugarcane.

Taxon
Sugarcanee0
Treatment
BR treatmente1
Gene
ShDRO2, ShDRO18, ShLAZY1e1
Outcome
qRT-PCRe1
Direction
upregulatede1

Not reportedComparator

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“qRT-PCR revealed that BR treatment significantly upregulated ShDRO2, ShDRO18, ShLAZY1, ShTAC1, and GRAS33”

✓ located verbatim in the source · abstract, characters 1294–1399 · show in text ↑
Intervention effectobservedoriginal resultsignificant (as stated)measured

Claim · model-written summary

BR treatment significantly upregulated ShTAC1 and GRAS33 in sugarcane.

Taxon
Sugarcanee0
Treatment
BR treatmente1
Gene
ShTAC1, and GRAS33e1
Outcome
qRT-PCRe1
Direction
upregulatede1

Not reportedComparator

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“qRT-PCR revealed that BR treatment significantly upregulated ShDRO2, ShDRO18, ShLAZY1, ShTAC1, and GRAS33”

✓ located verbatim in the source · abstract, characters 1294–1399 · show in text ↑
Associationobservedoriginal resultpositivemeasured

Claim · model-written summary

Under NaCl stress (250 mM), ShDRO2, ShDRO18 and ShKnox1 functioned as positive regulators in sugarcane.

Taxon
Sugarcanee0
Treatment
NaCl stress (250 mM)e1
Gene
ShDRO2, ShDRO18, ShKnox1e1
Outcome
positive regulatorse1
Direction
positivee1

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“Under NaCl stress (250 mM), five genes including, ShDRO2, ShDRO18, ShKnox1, ShGn1, and ShGRAS33 functioned as positive regulators”

✓ located verbatim in the source · abstract, characters 1473–1602 · show in text ↑
Associationobservedoriginal resultpositivemeasured

Claim · model-written summary

Under NaCl stress (250 mM), ShGn1 and ShGRAS33 functioned as positive regulators in sugarcane.

Taxon
Sugarcanee0
Treatment
NaCl stress (250 mM)e1
Gene
ShGn1, and ShGRAS33e1
Outcome
positive regulatorse1
Direction
positivee1

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“Under NaCl stress (250 mM), five genes including, ShDRO2, ShDRO18, ShKnox1, ShGn1, and ShGRAS33 functioned as positive regulators”

✓ located verbatim in the source · abstract, characters 1473–1602 · show in text ↑
Associationobservedoriginal resultnegativemeasured

Claim · model-written summary

Under NaCl stress, ShLg1 and ShTAC1 acted as negative regulators in sugarcane.

Taxon
Sugarcanee0
Treatment
NaCl stress (250 mM)e1
Gene
ShLg1 and ShTAC1e2
Outcome
negative regulatorse2
Direction
negativee2

Verbatim

e0

“Sugarcane, a major crop for sugar production”

✓ located verbatim in the source · abstract, characters 0–44 · show in text ↑
e1

“Under NaCl stress (250 mM), five genes including, ShDRO2, ShDRO18, ShKnox1, ShGn1, and ShGRAS33 functioned as positive regulators”

✓ located verbatim in the source · abstract, characters 1473–1602 · show in text ↑
e2

“while ShLg1 and ShTAC1 acted as negative regulators”

✓ located verbatim in the source · abstract, characters 1604–1655 · show in text ↑