This study demonstrates that PtWOX2 and PtWOX14 significantly accelerate the initiation of somatic embryos in Pinus massoniana, offering a comprehensive molecular framework to address conifer recalcitrance via PtWOX -mediated synergistic hormonal and transcriptional reprogramming.
Abstract
Somatic embryogenesis (SE) represents a powerful tool for conifer biotechnology, yet its application in
Pinus massoniana
is frequently hindered by severe genotype-dependent recalcitrance.
We identified two
WUSCHEL-related homeobox
(
WOX
) orthologs,
PtWOX2
and
PtWOX14
, as key regulators driving the embryogenic transition. By employing a genetic transformation system harboring the RUBY reporter for real-time visual selection, we demonstrated that ectopic expression of
PtWOX2
and
PtWOX14
dramatically accelerated SE initiation, with proembryogenic masses (PEMs) emerging 22.0-26.7 days earlier than in controls. Notably,
PtWOX
overexpression enabled the “fate reversal” of recalcitrant cell lines, transforming disorganized cell aggregates into highly polarized PEMs with distinct embryonal heads. Maturation capacity was increased by up to 1.7-fold in
PtWOX2
-overexpressing lines, whereas
PtWOX14
exhibited a genotype-dependent effect on somatic embryo yield. Physiological and WGCNA analyses revealed that
PtWOX
genes orchestrate a reciprocal hormonal reconfiguration, shifting the hormonal landscape from a high-auxin proliferative state to a low-IAA/high-ABA differentiation-permissive state. This transition is sustained by hierarchical regulatory networks in which
PtWOX2
and
PtWOX14
converge on an IAA-mediated execution module. This process involves the mobilization of master hubs such as
bHLH139
and
HB9
, to activate cell-wall and metabolic enzymes (
MAN1
,
Cht1
, and
EXPA1
) while relieving the transcriptional repression imposed by auxin signaling inhibitors like
IAA11
. Furthermore, protein interaction assays confirmed that PtWOX2 associates with nuclear partners such as Pt1G46750 and Pt5G39360, likely forming a post-translational regulatory complex to coordinate downstream developmental programs.
Our study demonstrates that
PtWOX2
and
PtWOX14
significantly accelerate the initiation of somatic embryos in
P. massoniana
, offering a comprehensive molecular framework to address conifer recalcitrance via
PtWOX
-mediated synergistic hormonal and transcriptional reprogramming. Furthermore, by establishing a genetic transformation system integrated with the RUBY reporter, this work provides a potential foundation for the genetic improvement and future large-scale propagation of
Pinus
species by enhancing early developmental efficiency.
This study constructed a pH-responsive P-TN/SF@Fe-Cur composite coating that demonstrated significant anti-infective, anti-inflammatory, antioxidant, pro-angiogenic, and pro-osteogenic effects in rat subcutaneous infection and femoral defect models.
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