By organism › Green plants › Byblidaceae

Method / resourceobservedoriginal resultpositivemeasured

Claim · model-written summary

A transformation protocol regenerated transgenic Byblis shoots within two months.

Taxon: Byblis guehoiByblis guehoit0
Treatment: hygromycin-containing Byblis Selection and Regeneration Medium (BSRM)e0
Outcome: transgenic shoots were regeneratede0
Value: within two monthse0

Verbatim

e0
“transgenic shoots were regenerated within two months on hygromycin-containing Byblis Selection and Regeneration Medium (BSRM)”
✓ located verbatim in the source · abstract, characters 491–616

t0
“Byblis guehoi”
✓ located verbatim in the source · title, characters 66–79

Title

Development of a rapid transformation and amplification system in Byblis guehoi unveils an atypical protein secretion pathway in sessile trichome cells

You-Xian Li; Chia-Hua Yu; I-Jou Hsu; et al. Plant and Cell Physiology 2026. doi:10.1093/pcp/pcag050

Other claims from this paper (8)

Method / resourceobservedoriginal resultpositivemeasured

Claim · model-written summary

The temporary immersion system enhanced growth and facilitated acclimation of transgenic lines.

Taxon: Byblis guehoiByblis guehoit0
Treatment: temporary immersion system (TIS)e0
Outcome: enhancing growth and facilitating acclimatione0

Not reportedComparator

Verbatim

e0
“a temporary immersion system (TIS) was implemented to rapidly propagate transgenic lines, enhancing growth and facilitating acclimation”
✓ located verbatim in the source · abstract, characters 631–766

t0
“Byblis guehoi”
✓ located verbatim in the source · title, characters 66–79

Title

Development of a rapid transformation and amplification system in Byblis guehoi unveils an atypical protein secretion pathway in sessile trichome cells

You-Xian Li; Chia-Hua Yu; I-Jou Hsu; et al. Plant and Cell Physiology 2026. doi:10.1093/pcp/pcag050

Other claims from this paper (8)

Method / resource A transformation protocol regenerated transgenic Byblis shoots within two months.
Method / resource The four constructs yielded transformation efficiencies of 24.9–59.4%.
Method / resource The constructs yielded regeneration efficiencies of 22.3–73.7%.
Observation mGFP5 signals were predominantly cytoplasmic in epidermal cells.
Observation CLV3sp-mGFP5 signals were localized to the plasma membrane in epidermal cells.
Observation Both constructs showed GFP at the plasma membrane and extracellular space of sessile trichome cells regardless of signal peptide.
Observation mGFP5 was secreted into mucilage independently of signal peptide presence.
Mechanism The authors propose the specialized cuticular pore as a possible interface for non-classical protein export.

Method / resourceobservedoriginal resultpositivemeasured

Claim · model-written summary

The four constructs yielded transformation efficiencies of 24.9–59.4%.

Taxon: Byblis guehoiByblis guehoit0
Outcome: transformation efficienciese0
Value: 24.9-59.4%e0

Verbatim

e0
“Four 35S promoter-driven constructs expressing GUS, RUBY, mGFP5, or CLV3sp-mGFP5 validated the protocol, yielding transformation efficiencies of 24.9-59.4%”
✓ located verbatim in the source · abstract, characters 768–923

t0
“Byblis guehoi”
✓ located verbatim in the source · title, characters 66–79

Title

Development of a rapid transformation and amplification system in Byblis guehoi unveils an atypical protein secretion pathway in sessile trichome cells

You-Xian Li; Chia-Hua Yu; I-Jou Hsu; et al. Plant and Cell Physiology 2026. doi:10.1093/pcp/pcag050

Other claims from this paper (8)

Method / resourceobservedoriginal resultpositivemeasured

Claim · model-written summary

The constructs yielded regeneration efficiencies of 22.3–73.7%.

Taxon: Byblis guehoiByblis guehoit0
Outcome: regeneration efficienciese0
Value: 22.3-73.7%e0

Verbatim

e0
“regeneration efficiencies of 22.3-73.7%”
✓ located verbatim in the source · abstract, characters 928–967

t0
“Byblis guehoi”
✓ located verbatim in the source · title, characters 66–79

Title

Development of a rapid transformation and amplification system in Byblis guehoi unveils an atypical protein secretion pathway in sessile trichome cells

You-Xian Li; Chia-Hua Yu; I-Jou Hsu; et al. Plant and Cell Physiology 2026. doi:10.1093/pcp/pcag050

Other claims from this paper (8)

Observationobservedoriginal resultmeasured

Claim · model-written summary

mGFP5 signals were predominantly cytoplasmic in epidermal cells.

Taxon: Byblis guehoiByblis guehoit0
Organ / stage: epidermal cellse0
Gene: mGFP5e0
Outcome: predominantly cytoplasmic signalse0

Not reportedDirection

Verbatim

e0
“predominantly cytoplasmic signals for mGFP5 and plasma membrane-localized signals for CLV3sp-mGFP5 in epidermal cells”
✓ located verbatim in the source · abstract, characters 998–1115

t0
“Byblis guehoi”
✓ located verbatim in the source · title, characters 66–79

Title

Development of a rapid transformation and amplification system in Byblis guehoi unveils an atypical protein secretion pathway in sessile trichome cells

You-Xian Li; Chia-Hua Yu; I-Jou Hsu; et al. Plant and Cell Physiology 2026. doi:10.1093/pcp/pcag050

Other claims from this paper (8)

Method / resource A transformation protocol regenerated transgenic Byblis shoots within two months.
Method / resource The temporary immersion system enhanced growth and facilitated acclimation of transgenic lines.
Method / resource The four constructs yielded transformation efficiencies of 24.9–59.4%.
Method / resource The constructs yielded regeneration efficiencies of 22.3–73.7%.
Observation CLV3sp-mGFP5 signals were localized to the plasma membrane in epidermal cells.
Observation Both constructs showed GFP at the plasma membrane and extracellular space of sessile trichome cells regardless of signal peptide.
Observation mGFP5 was secreted into mucilage independently of signal peptide presence.
Mechanism The authors propose the specialized cuticular pore as a possible interface for non-classical protein export.

Observationobservedoriginal resultmeasured

Claim · model-written summary

CLV3sp-mGFP5 signals were localized to the plasma membrane in epidermal cells.

Taxon: Byblis guehoiByblis guehoit0
Organ / stage: epidermal cellse0
Gene: CLV3sp-mGFP5e0
Outcome: plasma membrane-localized signalse0

Not reportedDirection

Verbatim

e0
“plasma membrane-localized signals for CLV3sp-mGFP5 in epidermal cells”
✓ located verbatim in the source · abstract, characters 1046–1115

t0
“Byblis guehoi”
✓ located verbatim in the source · title, characters 66–79

Title

Development of a rapid transformation and amplification system in Byblis guehoi unveils an atypical protein secretion pathway in sessile trichome cells

You-Xian Li; Chia-Hua Yu; I-Jou Hsu; et al. Plant and Cell Physiology 2026. doi:10.1093/pcp/pcag050

Other claims from this paper (8)

Method / resource A transformation protocol regenerated transgenic Byblis shoots within two months.
Method / resource The temporary immersion system enhanced growth and facilitated acclimation of transgenic lines.
Method / resource The four constructs yielded transformation efficiencies of 24.9–59.4%.
Method / resource The constructs yielded regeneration efficiencies of 22.3–73.7%.
Observation mGFP5 signals were predominantly cytoplasmic in epidermal cells.
Observation Both constructs showed GFP at the plasma membrane and extracellular space of sessile trichome cells regardless of signal peptide.
Observation mGFP5 was secreted into mucilage independently of signal peptide presence.
Mechanism The authors propose the specialized cuticular pore as a possible interface for non-classical protein export.

Observationobservedoriginal resultmeasured

Claim · model-written summary

Both constructs showed GFP at the plasma membrane and extracellular space of sessile trichome cells regardless of signal peptide.

Taxon: Byblis guehoiByblis guehoit0
Organ / stage: sessile trichome cellse0
Gene: GFPe0
Outcome: GFP signals at the plasma membrane and in the extracellular spacee0
Qualifier: regardless of the presence of a signal peptidee0

Not reportedDirection

Verbatim

e0
“both constructs exhibited GFP signals at the plasma membrane and in the extracellular space of sessile trichome cells, regardless of the presence of a signal peptide”
✓ located verbatim in the source · abstract, characters 1131–1296

t0
“Byblis guehoi”
✓ located verbatim in the source · title, characters 66–79

Title

Development of a rapid transformation and amplification system in Byblis guehoi unveils an atypical protein secretion pathway in sessile trichome cells

You-Xian Li; Chia-Hua Yu; I-Jou Hsu; et al. Plant and Cell Physiology 2026. doi:10.1093/pcp/pcag050

Other claims from this paper (8)

Method / resource A transformation protocol regenerated transgenic Byblis shoots within two months.
Method / resource The temporary immersion system enhanced growth and facilitated acclimation of transgenic lines.
Method / resource The four constructs yielded transformation efficiencies of 24.9–59.4%.
Method / resource The constructs yielded regeneration efficiencies of 22.3–73.7%.
Observation mGFP5 signals were predominantly cytoplasmic in epidermal cells.
Observation CLV3sp-mGFP5 signals were localized to the plasma membrane in epidermal cells.
Observation mGFP5 was secreted into mucilage independently of signal peptide presence.
Mechanism The authors propose the specialized cuticular pore as a possible interface for non-classical protein export.

Observationobservedoriginal resultmeasured

Claim · model-written summary

mGFP5 was secreted into mucilage independently of signal peptide presence.

Taxon: Byblis guehoiByblis guehoit0
Gene: mGFP5e0
Outcome: secreted into the mucilagee0
Qualifier: independently of signal peptide presencee0

Not reportedDirection

Verbatim

e0
“mGFP5 was secreted into the mucilage independently of signal peptide presence”
✓ located verbatim in the source · abstract, characters 1343–1420

t0
“Byblis guehoi”
✓ located verbatim in the source · title, characters 66–79

Title

Development of a rapid transformation and amplification system in Byblis guehoi unveils an atypical protein secretion pathway in sessile trichome cells

You-Xian Li; Chia-Hua Yu; I-Jou Hsu; et al. Plant and Cell Physiology 2026. doi:10.1093/pcp/pcag050

Other claims from this paper (8)

Method / resource A transformation protocol regenerated transgenic Byblis shoots within two months.
Method / resource The temporary immersion system enhanced growth and facilitated acclimation of transgenic lines.
Method / resource The four constructs yielded transformation efficiencies of 24.9–59.4%.
Method / resource The constructs yielded regeneration efficiencies of 22.3–73.7%.
Observation mGFP5 signals were predominantly cytoplasmic in epidermal cells.
Observation CLV3sp-mGFP5 signals were localized to the plasma membrane in epidermal cells.
Observation Both constructs showed GFP at the plasma membrane and extracellular space of sessile trichome cells regardless of signal peptide.
Mechanism The authors propose the specialized cuticular pore as a possible interface for non-classical protein export.

Mechanismhypothesisoriginal resultbasis n/a

Claim · model-written summary

The authors propose the specialized cuticular pore as a possible interface for non-classical protein export.

Taxon: Byblis guehoiByblis guehoit0
Organ / stage: sessile trichomese0
Outcome: non-classical protein exporte0
Qualifier: specialized cuticular pore lacking a rigid cell walle0

Verbatim

e0
“sessile trichomes of B. guehoi possess a specialized cuticular pore lacking a rigid cell wall, this structural feature may provide a plausible interface for non-classical protein export”
✓ located verbatim in the source · abstract, characters 1588–1773

t0
“Byblis guehoi”
✓ located verbatim in the source · title, characters 66–79

Title

Development of a rapid transformation and amplification system in Byblis guehoi unveils an atypical protein secretion pathway in sessile trichome cells

You-Xian Li; Chia-Hua Yu; I-Jou Hsu; et al. Plant and Cell Physiology 2026. doi:10.1093/pcp/pcag050

Other claims from this paper (8)

Method / resource A transformation protocol regenerated transgenic Byblis shoots within two months.
Method / resource The temporary immersion system enhanced growth and facilitated acclimation of transgenic lines.
Method / resource The four constructs yielded transformation efficiencies of 24.9–59.4%.
Method / resource The constructs yielded regeneration efficiencies of 22.3–73.7%.
Observation mGFP5 signals were predominantly cytoplasmic in epidermal cells.
Observation CLV3sp-mGFP5 signals were localized to the plasma membrane in epidermal cells.
Observation Both constructs showed GFP at the plasma membrane and extracellular space of sessile trichome cells regardless of signal peptide.
Observation mGFP5 was secreted into mucilage independently of signal peptide presence.

Intervention effectobservedoriginal resultpositivemeasured

Claim · model-written summary

Feeding Byblis filifolia with fruit flies increased the levels of hydrolytic digestive enzymes in its secreted fluid.

Taxon: Byblis filifoliaByblis filifoliat0
Treatment: experimental feeding with fruit fliese1
Interactor: fruit fliese1other
Outcome: hydrolytic digestive enzymese2
Direction: increasede2

Not reportedComparator

Verbatim

t0
“Byblis filifolia Planch.”
✓ located verbatim in the source · title, characters 30–54

e1
“after experimental feeding with fruit flies and coronatine application”
✓ located verbatim in the source · abstract, characters 530–600

e2
“Several hydrolytic digestive enzymes were identified in the secreted digestive fluid, the levels of which clearly increased in the presence of insect prey”
✓ located verbatim in the source · abstract, characters 602–756

Title

The carnivorous rainbow plant Byblis filifolia Planch. secretes digestive enzymes in response to prey capture independently of jasmonates

A. Pavlovič; T. Jílková; I. Chamrád; et al. Plant Biology 2025. doi:10.1111/plb.70029

Other claims from this paper (5)

Byblidaceae 164 claims

164 claims