bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Dec. 22, 2023
The
C4
photosynthetic
pathway
provided
a
major
advantage
to
plants
growing
in
hot,
dry
environments,
including
the
ancestors
of
our
most
productive
crops.
Two
traits
were
essential
for
evolution
this
pathway:
increased
vein
density
and
functionalization
bundle
sheath
cells
photosynthesis.
Although
GRAS
transcriptional
regulators,
SHORT
ROOT
(SHR),
have
been
implicated
mediating
leaf
patterning
both
C3
species,
little
is
known
about
what
controls
specialized
features
that
mediate
metabolism
physiology.
We
show
model
monocot,
Science,
Journal Year:
2025,
Volume and Issue:
387(6734), P. 666 - 673
Published: Feb. 6, 2025
Plants
grow
complex
root
systems
to
extract
unevenly
distributed
resources
from
soils.
Spatial
differences
in
soil
moisture
are
perceived
by
tips,
leading
the
patterning
of
new
branches
toward
available
water
a
process
called
hydropatterning.
Little
is
known
about
hydropatterning
behavior
and
its
genetic
basis
crop
plants.
Here,
we
developed
an
assay
measure
maize
revealed
substantial
between
tropical/subtropical
temperate
breeding
germplasm
that
likely
resulted
divergent
selection.
Genetic
analysis
confirmed
regulatory
role
auxin
gaseous
hormone
ethylene
locally
inhibits
branching
air-exposed
tissues.
Our
results
demonstrate
how
distinct
signaling
pathways
translate
spatial
patterns
availability
developmental
programs
determine
architecture.
Development,
Journal Year:
2024,
Volume and Issue:
151(20)
Published: Aug. 22, 2024
ABSTRACT
Grasses
form
morphologically
derived,
four-celled
stomata,
where
two
dumbbell-shaped
guard
cells
(GCs)
are
flanked
by
lateral
subsidiary
(SCs).
This
innovative
enables
rapid
opening
and
closing
kinetics
efficient
plant–atmosphere
gas
exchange.
The
mobile
bHLH
transcription
factor
MUTE
is
required
for
SC
formation
in
grasses.
Yet
whether
how
also
regulates
GC
development
mobility
recruitment
unclear.
Here,
we
transgenically
impaired
BdMUTE
from
to
precursors
the
emerging
model
grass
Brachypodium
distachyon.
Our
data
indicate
that
reduced
severely
affected
spatiotemporal
coordination
of
development.
Furthermore,
although
has
a
cell-autonomous
role
division
orientation,
complete
dumbbell
morphogenesis
GCs
recruitment.
Finally,
leaf-level
exchange
measurements
showed
dosage-dependent
complementation
morphology
was
mirrored
gradual
physiological
stomatal
kinetics.
Together,
our
work
revealed
dual
regulating
orientation
recruitment,
which
turn
stomata.
New Phytologist,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
Summary
Drought
stress
imposes
severe
challenges
on
agriculture
by
impacting
crop
performance.
Understanding
drought
responses
in
plants
at
a
cellular
level
is
crucial
first
step
toward
engineering
improved
resilience.
However,
the
molecular
to
are
complex
as
they
depend
multiple
factors,
including
severity
of
drought,
profiled
organ,
its
developmental
stage
or
even
cell
types
therein.
Thus,
deciphering
transcriptional
especially
challenging.
In
this
study,
we
investigated
tissue‐specific
mild
(MD)
young
Arabidopsis
thaliana
(Arabidopsis)
leaves
using
single‐cell
RNA
sequencing
(scRNA‐seq).
To
preserve
integrity
during
isolation,
inhibited
synthesis
transcription
inhibitor
actinomycin
D,
and
demonstrated
benefits
transcriptome
fixation
for
studying
level.
We
present
curated
validated
atlas,
comprising
50
797
high‐quality
cells
from
almost
all
known
leaf.
All
type
annotations
were
with
new
library
reporter
lines.
The
data
available
broad
community
an
intuitive
tool
browsable
atlas
(
http://www.single‐cell.be/plant/leaf‐drought
).
show
that
mesophyll
contains
two
spatially
separated
populations
distinct
drought:
one
enriched
canonical
abscisic
acid‐related
drought‐responsive
genes,
another
genes
involved
iron
starvation
responses.
Our
study
thus
reveals
dual
adaptive
mechanism
leaf
response
MD
provides
valuable
resource
future
research
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 27, 2024
Abstract
Plants
grow
complex
root
systems
to
extract
unevenly
distributed
resources
from
soils.
Spatial
differences
in
soil
moisture
are
perceived
by
tips
leading
the
patterning
of
new
branches
towards
available
water,
a
process
called
hydropatterning.
Little
is
known
about
hydropatterning
behavior
and
its
genetic
basis
crops
plants.
Here,
we
develop
an
assay
measure
maize
reveal
substantial
between
tropical/subtropical
temperate
breeding
germplasm
that
likely
resulted
divergent
selection.
Genetic
dissection
confirmed
regulatory
role
auxin
revealed
gaseous
hormone
ethylene
acts
locally
inhibit
branching
air-exposed
tissues.
These
findings
demonstrate
crop
relevance
establish
basis.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Nov. 28, 2023
The
plasticity
of
plant
cells
underlies
their
wide
capacity
to
regenerate,
with
increasing
evidence
in
plants
and
animals
implicating
cell
cycle
dynamics
cellular
reprogramming.
To
investigate
the
during
reprogramming,
we
developed
a
comprehensive
set
phase
markers
Arabidopsis
root.
Using
single-cell
RNA-seq
profiles
live
imaging
regeneration,
found
that
subset
near
an
ablation
injury
dramatically
increases
division
rate
by
truncating
G1.
Cells
G1
undergo
transient
nuclear
peak
glutathione
(GSH)
prior
coordinated
entry
into
S
followed
rapid
divisions
A
symplastic
block
ground
tissue
impairs
which
is
rescued
exogenous
GSH.
We
propose
model
GSH
from
outer
tissues
released
upon
licensing
exit
wound
induce
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 31, 2024
ABSTRACT
Background
Recent
developments
in
hybridization
chain
reaction
(HCR)
have
enabled
robust
simultaneous
localization
of
multiple
mRNA
transcripts
using
fluorescence
situ
(FISH).
Once
split
initiator
oligonucleotide
probes
bind
their
target
mRNA,
HCR
uses
DNA
base-pairing
fluorophore-labeled
hairpin
sets
to
self-assemble
into
large
polymers,
amplifying
the
signal
and
reducing
non-specific
background.
Few
studies
applied
plants,
despite
its
demonstrated
utility
whole
mount
animal
tissues
cell
culture.
Our
aim
was
optimize
this
technique
for
sectioned
plant
embedded
with
paraffin
methacrylate
resins,
test
combination
immunolocalization
subsequent
correlation
ultrastructure
scanning
electron
microscopy.
Results
Application
10
µm
sections
17-day-old
Setaria
viridis
(green
millet)
inflorescences
confocal
microscopy
revealed
that
transcription
factor
KNOTTED
1
(
KN1
)
were
localized
developing
floret
meristem
vascular
tissue
while
SHATTERING
SH1
MYB26
co-localized
breakpoint
below
floral
structures
(the
abscission
zone).
We
also
used
de-embedment
1.5
0.5
3-day-old
Arabidopsis
thaliana
seedlings
show
specific
CHLOROPHYLL
BINDING
FACTOR
a/b
CAB1
highly
expressed
photosynthetic
ELONGATION
ALPHA
EF1
α
meristematic
shoot
apex.
The
housekeeping
gene
ACTIN7
ACT7
more
uniformly
distributed
reduced
signals
lattice
structured-illumination
followed
by
backscattered
imaging
thus
demonstrating
feasibility
correlating
fluorescent
ultrastructure.
Conclusion
successfully
adapted
use
both
on
diverse
two
model
organisms,
allowing
concurrent
cellular
subcellular
mRNAs,
antibodies
other
affinity
probe
classes.
mild
conditions
made
it
amenable
observe
immunofluorescence
same
section.
De-embedded
semi-thin
compatible
correlative
approaches.
protocol
provides
numerous
practical
tips
successful
labeling
microscopy-compatible,
material.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 9, 2024
ABSTRACT
Single-molecule
fluorescence
in
situ
hybridization
(smFISH)
has
emerged
as
a
powerful
tool
to
study
gene
expression
dynamics
with
unparalleled
precision
and
spatial
resolution
variety
of
biological
systems.
Recent
advancements
have
expanded
its
application
encompass
plant
studies,
yet
demand
persists
for
simple
robust
smFISH
method
adapted
tissue
sections.
Here,
we
present
an
optimized
protocol
(cryo-smFISH)
visualizing
quantifying
single
mRNA
molecules
cryosections.
This
exhibits
remarkable
sensitivity,
capable
detecting
low-expression
transcripts,
including
long
non-coding
RNAs.
Integrating
deep
learning-based
algorithm
our
image
analysis
pipeline,
enables
us
assign
RNA
abundance
precisely
nuclear
cytoplasmic
compartments.
Compatibility
Immunofluorescence
also
allows
endogenous
proteins
be
visualized
quantified
simultaneously.
Finally,
this
presents
the
first
time
use
single-cell
sequencing
(scRNA-seq)
validation
plants.
By
extending
cryosections,
even
broader
community
scientists
will
able
exploit
multiple
potentials
quantitative
transcript
at
cellular
subcellular
resolutions.