BioDesign Research,
Год журнала:
2024,
Номер
6, С. 0029 - 0029
Опубликована: Янв. 1, 2024
Plants
are
complex
systems
hierarchically
organized
and
composed
of
various
cell
types.
To
understand
the
molecular
underpinnings
plant
systems,
single-cell
RNA
sequencing
(scRNA-seq)
has
emerged
as
a
powerful
tool
for
revealing
high
resolution
gene
expression
patterns
at
cellular
level
investigating
cell-type
heterogeneity.
Furthermore,
scRNA-seq
analysis
biosystems
great
potential
generating
new
knowledge
to
inform
design
synthetic
biology,
which
aims
modify
plants
genetically/epigenetically
through
genome
editing,
engineering,
or
re-writing
based
on
rational
increasing
crop
yield
quality,
promoting
bioeconomy
enhancing
environmental
sustainability.
In
particular,
data
from
studies
can
be
utilized
facilitate
development
high-precision
Build-Design-Test-Learn
capabilities
maximizing
targeted
performance
engineered
while
minimizing
unintended
side
effects.
date,
been
demonstrated
in
limited
number
species,
including
model
(e.g.,
Arabidopsis
thaliana),
agricultural
crops
Oryza
sativa),
bioenergy
Populus
spp.).
It
is
expected
that
future
technical
advancements
will
reduce
cost
consequently
accelerate
application
this
emerging
technology
plants.
review,
we
summarize
current
scRNA-seq,
sample
preparation,
sequencing,
analysis,
provide
guidance
how
choose
appropriate
methods
different
types
samples.
We
then
highlight
applications
both
biology
research.
Finally,
discuss
challenges
opportunities
Abstract
Background
The
epidermis
of
cotton
ovule
produces
fibers,
the
most
important
natural
cellulose
source
for
global
textile
industry.
However,
molecular
mechanism
fiber
cell
growth
is
still
poorly
understood.
Results
Here,
we
develop
an
optimized
protoplasting
method,
and
integrate
single-cell
RNA
sequencing
(scRNA-seq)
ATAC
(scATAC-seq)
to
systematically
characterize
cells
outer
integument
ovules
from
wild
type
fuzzless/lintless
(
fl
)
(Gossypium
hirsutum
).
By
jointly
analyzing
scRNA-seq
data
wildtype
fl,
identify
five
populations
including
construct
development
trajectory
lineage
cells.
Interestingly,
by
time-course
diurnal
transcriptomic
analysis,
demonstrate
that
primary
a
highly
regulated
circadian
rhythmic
process.
Moreover,
small
peptide
GhRALF1
rhythmically
controls
possibly
through
oscillating
auxin
signaling
proton
pump
activity
in
plasma
membrane.
Combining
with
scATAC-seq,
further
two
cardinal
cis-regulatory
elements
(CREs,
TCP
motif,
TCP-like
motif)
which
are
bound
trans
factors
GhTCP14s
modulate
metabolism
mitochondria
protein
translation
regulating
approximately
one
third
genes
expressed
Conclusions
We
uncover
fiber-specific
clock-controlled
gene
expression
program
growth.
This
study
unprecedentedly
reveals
new
route
improve
traits
engineering
clock
Plant Communications,
Год журнала:
2023,
Номер
4(5), С. 100630 - 100630
Опубликована: Май 25, 2023
Taxus
leaves
provide
the
raw
industrial
materials
for
taxol,
a
natural
antineoplastic
drug
widely
used
in
treatment
of
various
cancers.
However,
precise
distribution,
biosynthesis,
and
transcriptional
regulation
taxoids
other
active
components
remain
unknown.
Matrix-assisted
laser
desorption/ionization-mass
spectrometry
imaging
analysis
was
to
visualize
secondary
metabolites
leaf
sections
mairei,
confirming
tissue-specific
accumulation
different
metabolites.
Single-cell
sequencing
produce
expression
profiles
8846
cells,
with
median
2352
genes
per
cell.
Based
on
series
cluster-specific
markers,
cells
were
grouped
into
15
clusters,
suggesting
high
degree
cell
heterogeneity
T.
mairei
leaves.
Our
data
create
first
metabolic
single-cell
atlas
reveal
spatial
temporal
patterns
several
pathways.
According
cell-type
annotation,
most
taxol
biosynthesis
are
expressed
mainly
mesophyll
cells;
phenolic
acid
flavonoid
highly
epidermal
(including
stomatal
complex
guard
cells);
terpenoid
steroid
specifically
cells.
A
number
novel
cell-specific
transcription
factors
involved
metabolite
identified,
including
MYB17,
WRKY12,
WRKY31,
ERF13,
GT_2,
bHLH46.
research
establishes
landscape
major
types
at
resolution
provides
valuable
resources
studying
basic
principles
cell-type-specific
metabolism.
Molecular Plant,
Год журнала:
2023,
Номер
16(12), С. 1990 - 2003
Опубликована: Окт. 17, 2023
Plants
can
synthesize
a
wide
range
of
terpenoids
in
response
to
various
environmental
cues.
However,
the
specific
regulatory
mechanisms
governing
terpenoid
biosynthesis
at
cellular
level
remain
largely
elusive.
In
this
study,
we
employed
single-cell
RNA
sequencing
comprehensively
characterize
transcriptome
profile
cotton
leaves
and
established
hierarchical
transcriptional
network
regulating
cell-specific
production.
We
observed
substantial
expression
levels
genes
associated
with
both
volatile
terpenes
(such
as
β-caryophyllene
β-myrcene)
non-volatile
gossypol-type
secretory
glandular
cells.
Moreover,
two
novel
transcription
factors,
namely
GoHSFA4a
GoNAC42,
are
identified
function
downstream
Gossypium
PIGMENT
GLAND
FORMATION
genes.
Both
factors
could
directly
regulate
biosynthetic
cells
developmental
stimuli.
For
convenient
retrieval
data
generated
developed
user-friendly
web
server
.
Our
findings
not
only
offer
valuable
insights
into
precise
regulation
but
also
provide
potential
targets
for
breeding
endeavors.
Cell Reports,
Год журнала:
2024,
Номер
43(2), С. 113747 - 113747
Опубликована: Фев. 1, 2024
Legumes
establish
a
symbiotic
relationship
with
nitrogen-fixing
rhizobia
by
developing
nodules.
Nodules
are
modified
lateral
roots
that
undergo
changes
in
their
cellular
development
response
to
bacteria,
but
the
transcriptional
reprogramming
occurs
these
root
cells
remains
largely
uncharacterized.
Here,
we
describe
cell-type-specific
transcriptome
of
Medicago
truncatula
during
early
nodule
wild-type
genotype
Jemalong
A17,
complemented
hypernodulating
mutant
(sunn-4)
expand
cell
population
responding
infection
and
subsequent
biological
inferences.
The
analysis
identifies
epidermal
hair
stele
sub-cell
types
associated
regulation
proliferation.
Trajectory
inference
shows
cortex-derived
lineages
differentiating
form
primordia
and,
posteriorly,
its
meristem,
while
modulating
phytohormone-related
genes.
Gene
regulatory
transcriptomes
new
regulators
nodulation,
including
STYLISH
4,
for
which
function
is
validated.
BioDesign Research,
Год журнала:
2024,
Номер
6, С. 0029 - 0029
Опубликована: Янв. 1, 2024
Plants
are
complex
systems
hierarchically
organized
and
composed
of
various
cell
types.
To
understand
the
molecular
underpinnings
plant
systems,
single-cell
RNA
sequencing
(scRNA-seq)
has
emerged
as
a
powerful
tool
for
revealing
high
resolution
gene
expression
patterns
at
cellular
level
investigating
cell-type
heterogeneity.
Furthermore,
scRNA-seq
analysis
biosystems
great
potential
generating
new
knowledge
to
inform
design
synthetic
biology,
which
aims
modify
plants
genetically/epigenetically
through
genome
editing,
engineering,
or
re-writing
based
on
rational
increasing
crop
yield
quality,
promoting
bioeconomy
enhancing
environmental
sustainability.
In
particular,
data
from
studies
can
be
utilized
facilitate
development
high-precision
Build-Design-Test-Learn
capabilities
maximizing
targeted
performance
engineered
while
minimizing
unintended
side
effects.
date,
been
demonstrated
in
limited
number
species,
including
model
(e.g.,
Arabidopsis
thaliana),
agricultural
crops
Oryza
sativa),
bioenergy
Populus
spp.).
It
is
expected
that
future
technical
advancements
will
reduce
cost
consequently
accelerate
application
this
emerging
technology
plants.
review,
we
summarize
current
scRNA-seq,
sample
preparation,
sequencing,
analysis,
provide
guidance
how
choose
appropriate
methods
different
types
samples.
We
then
highlight
applications
both
biology
research.
Finally,
discuss
challenges
opportunities