Paper · 2024 · Frontiers in Plant Science

Signaling pathways mediating the induction of preharvest fruit drop in litchi

Jun Wang; Wuqiang Ma; Fei Wang; et al.

15
claims
15
verbatim quotes
6
citations
5
research areas
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Open access · cc-by

Abstract

Certain litchi varieties, such as “Nuomici”, are highly susceptible to preharvest fruit drop, which leads to significant losses in fruit yield and economic value. However, the precise molecular mechanisms underlying this issue are not yet fully understood. In this study, we aimed to elucidate the signaling pathways that facilitate preharvest fruit drop in litchi, using “Nuomici” and “Huaizhi” cultivars as examples, which demonstrate high and low preharvest fruit drop rates, respectively. Our findings revealed that “Nuomici” experienced a substantial preharvest fruit drop, with a cumulative rate of 41.68%, significantly higher than the 1.44% observed in “Huaizhi”. Cellulase activity assays showed a significant increase in cellulase activity in the abscission zone of “Nuomici”, which coincided with the occurrence of preharvest fruit drop, in contrast to the relatively low levels in “Huaizhi”. Phytohormone assays indicated lower indole-3-acetic acid content in the pericarp, aril, and seeds of “Nuomici” during the preharvest stage compared to “Huaizhi”, coupled with higher abscisic acid levels in the seeds of “Nuomici”. Furthermore, transcriptomic analysis identified 180, 282, 655, and 241 differentially expressed genes (DEGs) in the pericarp, aril, seed, and abscission zone, respectively, between the two cultivars during preharvest fruit drop. These DEGs are intricately involved in the generation and transmission of abscission signals from fruit tissues, encompassing PIN , PIN-LIKES , LAX , and SAUR genes related to polar auxin transport, ethylene diffusion, as well as perceiving these signals and activating the abscission process within the abscission zone. This includes ACO and ILR genes involved in hormone biosynthesis and signal transduction, regulation by WRKY, NAC, and bHLH transcription factors, AAO genes involved in response to reactive oxygen species, and EXP, EG, and PG genes involved in cell wall degradation in the abscission zone. Based on these comprehensive findings, we propose a model for preharvest fruit drop triggered by a series of molecular events in litchi, providing valuable insights into the complex mechanisms governing this phenomenon.

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Claims 15

Associationobservedoriginal resultnegativesignificant (as stated)measured

Claim · model-written summary

Nuomici had 41.68% cumulative fruit drop versus 1.44% in Huaizhi.

Material
“Nuomici”e0
Outcome
preharvest fruit drope0
Direction
highere0
Value
41.68%e0
Qualifier
1.44%e0
Comparator
“Huaizhi”e0

Not reportedTaxon

Verbatim

e0

““Nuomici” experienced a substantial preharvest fruit drop, with a cumulative rate of 41.68%, significantly higher than the 1.44% observed in “Huaizhi””

✓ located verbatim in the source · abstract, characters 520–670 · show in text ↑
Associationobservedoriginal resultnegativesignificant (as stated)measured

Claim · model-written summary

Cellulase activity rose in the Nuomici abscission zone as fruit drop occurred, compared with Huaizhi.

Material
“Nuomici”e0
Organ / stage
abscission zonee0
Gene
cellulasee0
Outcome
cellulase activitye0
Direction
increasee0
Comparator
“Huaizhi”e0

Not reportedTaxon

Verbatim

e0

“significant increase in cellulase activity in the abscission zone of “Nuomici”, which coincided with the occurrence of preharvest fruit drop, in contrast to the relatively low levels in “Huaizhi””

✓ located verbatim in the source · abstract, characters 707–902 · show in text ↑
Associationobservedoriginal resultnegativemeasured

Claim · model-written summary

Nuomici pericarp had lower indole-3-acetic acid content than Huaizhi before harvest.

Material
“Nuomici”e0
Organ / stage
pericarpe0
Outcome
indole-3-acetic acid contente0
Direction
lowere0
Comparator
“Huaizhi”e0

Not reportedTaxon

Verbatim

e0

“lower indole-3-acetic acid content in the pericarp, aril, and seeds of “Nuomici” during the preharvest stage compared to “Huaizhi””

✓ located verbatim in the source · abstract, characters 934–1064 · show in text ↑
Associationobservedoriginal resultnegativemeasured

Claim · model-written summary

Nuomici aril had lower indole-3-acetic acid content than Huaizhi before harvest.

Material
“Nuomici”e0
Organ / stage
arile0
Outcome
indole-3-acetic acid contente0
Direction
lowere0
Comparator
“Huaizhi”e0

Not reportedTaxon

Verbatim

e0

“lower indole-3-acetic acid content in the pericarp, aril, and seeds of “Nuomici” during the preharvest stage compared to “Huaizhi””

✓ located verbatim in the source · abstract, characters 934–1064 · show in text ↑
Associationobservedoriginal resultnegativemeasured

Claim · model-written summary

Nuomici seeds had lower indole-3-acetic acid content than Huaizhi before harvest.

Material
“Nuomici”e0
Organ / stage
seedse0
Outcome
indole-3-acetic acid contente0
Direction
lowere0
Comparator
“Huaizhi”e0

Not reportedTaxon

Verbatim

e0

“lower indole-3-acetic acid content in the pericarp, aril, and seeds of “Nuomici” during the preharvest stage compared to “Huaizhi””

✓ located verbatim in the source · abstract, characters 934–1064 · show in text ↑
Associationobservedoriginal resultnegativemeasured

Claim · model-written summary

Nuomici seeds had higher abscisic acid levels than Huaizhi.

Material
“Nuomici”e0
Organ / stage
seedse0
Outcome
abscisic acid levelse0
Direction
highere0

Not reportedTaxon

Verbatim

e0

“higher abscisic acid levels in the seeds of “Nuomici””

✓ located verbatim in the source · abstract, characters 1079–1132 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Pericarp had 180 differentially expressed genes between cultivars.

Organ / stage
pericarpe0
Outcome
differentially expressed genes (DEGs)e0
Value
180e0

Not reportedTaxon

Verbatim

e0

“identified 180, 282, 655, and 241 differentially expressed genes (DEGs) in the pericarp, aril, seed, and abscission zone, respectively”

✓ located verbatim in the source · abstract, characters 1171–1305 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Aril had 282 differentially expressed genes between cultivars.

Organ / stage
arile0
Outcome
differentially expressed genes (DEGs)e0
Value
282e0

Not reportedTaxon

Verbatim

e0

“identified 180, 282, 655, and 241 differentially expressed genes (DEGs) in the pericarp, aril, seed, and abscission zone, respectively”

✓ located verbatim in the source · abstract, characters 1171–1305 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Seed had 655 differentially expressed genes between cultivars.

Organ / stage
seede0
Outcome
differentially expressed genes (DEGs)e0
Value
655e0

Not reportedTaxon

Verbatim

e0

“identified 180, 282, 655, and 241 differentially expressed genes (DEGs) in the pericarp, aril, seed, and abscission zone, respectively”

✓ located verbatim in the source · abstract, characters 1171–1305 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

Abscission zone had 241 differentially expressed genes between cultivars.

Organ / stage
abscission zonee0
Outcome
differentially expressed genes (DEGs)e0
Value
241e0

Not reportedTaxon

Verbatim

e0

“identified 180, 282, 655, and 241 differentially expressed genes (DEGs) in the pericarp, aril, seed, and abscission zone, respectively”

✓ located verbatim in the source · abstract, characters 1171–1305 · show in text ↑
Mechanismobservedoriginal resultmeasured

Claim · model-written summary

PIN, PIN-LIKES, LAX and SAUR genes were implicated in polar auxin transport and abscission signaling.

Gene
PIN , PIN-LIKES , LAX , and SAURe0
Outcome
polar auxin transporte0

Not reportedTaxon

Verbatim

e0

“PIN , PIN-LIKES , LAX , and SAUR genes related to polar auxin transport”

✓ located verbatim in the source · abstract, characters 1489–1560 · show in text ↑
Mechanismobservedoriginal resultmeasured

Claim · model-written summary

ACO and ILR genes were implicated in hormone biosynthesis and signaling.

Gene
ACO and ILRe0
Outcome
hormone biosynthesis and signal transductione0

Not reportedTaxon

Verbatim

e0

“ACO and ILR genes involved in hormone biosynthesis and signal transduction”

✓ located verbatim in the source · abstract, characters 1698–1772 · show in text ↑
Mechanismobservedoriginal resultmeasured

Claim · model-written summary

WRKY, NAC and bHLH transcription factors were implicated in abscission regulation.

Gene
WRKY, NAC, and bHLHe0
Outcome
regulatione0

Not reportedTaxon

Verbatim

e0

“regulation by WRKY, NAC, and bHLH transcription factors”

✓ located verbatim in the source · abstract, characters 1774–1829 · show in text ↑
Mechanismobservedoriginal resultmeasured

Claim · model-written summary

AAO genes were implicated in reactive oxygen species response.

Gene
AAOe0
Outcome
response to reactive oxygen speciese0

Not reportedTaxon

Verbatim

e0

“AAO genes involved in response to reactive oxygen species”

✓ located verbatim in the source · abstract, characters 1831–1888 · show in text ↑
Mechanismobservedoriginal resultmeasured

Claim · model-written summary

EXP, EG and PG genes were implicated in cell wall degradation in the abscission zone.

Organ / stage
abscission zonee0
Gene
EXP, EG, and PGe0
Outcome
cell wall degradatione0

Not reportedTaxon

Verbatim

e0

“EXP, EG, and PG genes involved in cell wall degradation in the abscission zone”

✓ located verbatim in the source · abstract, characters 1894–1972 · show in text ↑