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A conserved and predictable pluripotency window in callus unlocks efficient transformation in grasses and beyond
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SUMMARY
A major bottleneck in plant biotechnology is the inefficient and genotype-dependent regeneration of callus, which severely limits genetic transformation and functional studies across many species. This barrier is acutely exemplified in the study of beneficial plant-microbe interactions, such as the
Epichloë
-grass symbiosis—a system conferring remarkable stress tolerance to its host but hindered by a lack of efficient genetic tools. To address this, we established a chromosome-scale genome for an
Epichloë
native host grass
Achnatherum inebrians
. We discovered that the expression dynamics of evolutionarily conserved cell pluripotency regulators (CPRs) including
ARF5/7/19, BBM, WUS/WOX5
and
CUC1/2
serve as a precise molecular predictor for callus regenerative capacity, revealing that pluripotency is dynamic and peaks within a narrow, definable time window. Harnessing this predictable window enabled the development of a highly efficient transformation system for
A. inebrians
(49.4% efficiency). Crucially, this CPR-based strategy proved generalizable: applied to wheat and the legume sainfoin, it pinpointed species-specific optimal regeneration windows, boosting shoot regeneration rates to 65.7% and 87.5%, respectively. Collectively, our work provides an integrated research system and a rational design principle that removes a key barrier to uncovering molecular mechanisms in plant systems, particularly the
Epichloë
-enhanced stress tolerance symbiosis.
Title: A conserved and predictable pluripotency window in callus unlocks efficient transformation in grasses and beyond
Description:
SUMMARY
A major bottleneck in plant biotechnology is the inefficient and genotype-dependent regeneration of callus, which severely limits genetic transformation and functional studies across many species.
This barrier is acutely exemplified in the study of beneficial plant-microbe interactions, such as the
Epichloë
-grass symbiosis—a system conferring remarkable stress tolerance to its host but hindered by a lack of efficient genetic tools.
To address this, we established a chromosome-scale genome for an
Epichloë
native host grass
Achnatherum inebrians
.
We discovered that the expression dynamics of evolutionarily conserved cell pluripotency regulators (CPRs) including
ARF5/7/19, BBM, WUS/WOX5
and
CUC1/2
serve as a precise molecular predictor for callus regenerative capacity, revealing that pluripotency is dynamic and peaks within a narrow, definable time window.
Harnessing this predictable window enabled the development of a highly efficient transformation system for
A.
inebrians
(49.
4% efficiency).
Crucially, this CPR-based strategy proved generalizable: applied to wheat and the legume sainfoin, it pinpointed species-specific optimal regeneration windows, boosting shoot regeneration rates to 65.
7% and 87.
5%, respectively.
Collectively, our work provides an integrated research system and a rational design principle that removes a key barrier to uncovering molecular mechanisms in plant systems, particularly the
Epichloë
-enhanced stress tolerance symbiosis.
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