Ciliary
motility
is
driven
by
axonemal
dyneins
that
are
assembled
in
the
cytoplasm
before
deployment
to
cilia.
Motile
ciliopathy
can
result
from
defects
themselves
or
factors
required
for
their
cytoplasmic
pre-assembly.
Recent
work
demonstrates
dyneins,
specific
assembly
factors,
and
broadly-acting
chaperones
concentrated
liquid-like
organelles
called
DynAPs
(Dynein
Axonemal
Particles).
Here,
we
use
Mapping
the
vertebrate
developmental
landscape
As
embryos
develop,
numerous
cell
types
with
distinct
functions
and
morphologies
arise
from
pluripotent
cells.
Three
research
groups
have
used
single-cell
RNA
sequencing
to
analyze
transcriptional
changes
accompanying
development
of
(see
Perspective
by
Harland).
Wagner
et
al.
sequenced
transcriptomes
more
than
90,000
cells
throughout
zebrafish
reveal
how
differentiate
during
axis
patterning,
germ
layer
formation,
early
organogenesis.
Farrell
profiled
tens
thousands
embryonic
applied
a
computational
approach
construct
branching
tree
describing
trajectories
that
lead
25
types.
The
revealed
change
their
gene
expression
as
they
become
specialized.
Briggs
examined
whole
frog
embryos,
spanning
zygotic
genome
activation
through
organogenesis,
map
states
differentiation
across
all
lineages
over
time.
These
data
approaches
pave
way
for
comprehensive
reconstruction
development.
Science
,
this
issue
p.
981
eaar3131
eaar5780
;
see
also
967
Nucleic Acids Research,
Год журнала:
2018,
Номер
47(D1), С. D786 - D792
Опубликована: Окт. 4, 2018
The
HUGO
Gene
Nomenclature
Committee
(HGNC)
based
at
EMBL's
European
Bioinformatics
Institute
(EMBL-EBI)
assigns
unique
symbols
and
names
to
human
genes.
There
are
over
40
000
approved
gene
in
our
current
database
of
which
19
for
protein-coding
Vertebrate
(VGNC)
was
established
2016
assign
standardized
nomenclature
line
with
vertebrate
species
that
lack
their
own
committees.
VGNC
initially
assigned
15000
genes
chimpanzee.
We
have
extended
this
process
other
species,
naming
14000
cow
dog
13
horse
date.
Our
HGNC
website
https://www.genenames.org
has
undergone
a
major
design
update,
simplifying
the
homepage
provide
easy
access
search
tools
making
site
more
mobile
friendly.
families
pages
now
known
as
'gene
groups'
increased
number
1200,
nearly
half
all
named
currently
least
one
group.
This
article
provides
an
overview
online
data
resources,
focusing
on
work
last
two
years.
Science,
Год журнала:
2021,
Номер
372(6545), С. 984 - 989
Опубликована: Май 27, 2021
We
investigated
genome
folding
across
the
eukaryotic
tree
of
life.
find
two
types
three-dimensional
(3D)
architectures
at
chromosome
scale.
Each
type
appears
and
disappears
repeatedly
during
evolution.
The
architecture
that
an
organism
exhibits
correlates
with
absence
condensin
II
subunits.
Moreover,
depletion
converts
human
to
a
state
resembling
seen
in
organisms
such
as
fungi
or
mosquitoes.
In
this
state,
centromeres
cluster
together
nucleoli,
heterochromatin
domains
merge.
propose
physical
model
which
lengthwise
compaction
chromosomes
by
mitosis
determines
chromosome-scale
architecture,
effects
are
retained
subsequent
interphase.
This
mechanism
likely
has
been
conserved
since
last
common
ancestor
all
eukaryotes.
Nucleic Acids Research,
Год журнала:
2020,
Номер
49(D1), С. D831 - D847
Опубликована: Сен. 15, 2020
Abstract
Bgee
is
a
database
to
retrieve
and
compare
gene
expression
patterns
in
multiple
animal
species,
produced
by
integrating
data
types
(RNA-Seq,
Affymetrix,
situ
hybridization,
EST
data).
It
based
exclusively
on
curated
healthy
wild-type
(e.g.,
no
knock-out,
treatment,
disease),
provide
comparable
reference
of
normal
expression.
Curation
includes
very
large
datasets
such
as
GTEx
(re-annotation
samples
‘healthy’
or
not)
well
many
small
ones.
Data
are
integrated
made
between
species
thanks
consistent
annotation
processing,
calls
presence/absence
expression,
along
with
scores.
As
result,
capable
detecting
the
conditions
any
single
gene,
accommodating
type
species.
provides
several
tools
for
analyses,
allowing,
e.g.,
automated
comparisons
within
retrieval
prefered
enrichment
analyses
sets
genes.
release
14.1
29
available
at
https://bgee.org/
through
its
Bioconductor
R
package
BgeeDB.
Abstract
Xenbase
(https://www.xenbase.org/),
the
Xenopus
model
organism
knowledgebase,
is
a
web-accessible
resource
that
integrates
diverse
genomic
and
biological
data
from
research
on
laboratory
frogs
laevis
tropicalis.
The
goal
of
to
accelerate
discovery
empower
research,
enhance
impact
data,
facilitate
dissemination
these
data.
also
enhances
value
through
high-quality
curation,
integration,
providing
bioinformatics
tools
optimized
for
experiments,
linking
human
other
organisms.
plays
an
indispensable
role
in
making
interoperable
accessible
broader
biomedical
community
accordance
with
FAIR
principles.
provides
annotated
updates
organizations
such
as
NCBI,
UniProtKB,
Ensembl,
Gene
Ontology
consortium,
most
recently,
Alliance
Genomic
Resources,
common
clearing
house
humans
This
article
brief
overview
key
recently
added
features
Xenbase.
New
include
processing
high-throughput
sequencing
NCBI
Expression
Omnibus;
curation
anatomical,
physiological,
expression
phenotypes
newly
created
Phenotype
Ontology;
annotations;
new
anatomical
drawings
Normal
Table
development;
integration
latest
v10.1
genome
annotations.
Finally,
we
highlight
areas
future
development
at
continue
support
community.
Analytical Chemistry,
Год журнала:
2019,
Номер
91(7), С. 4797 - 4805
Опубликована: Март 3, 2019
Label-free
single-cell
proteomics
by
mass
spectrometry
(MS)
is
currently
incompatible
with
complex
tissues
without
requiring
cell
culturing,
dissection,
or
tissue
dissociation.
We
here
report
the
first
example
of
label-free
MS-based
directly
in
single
cells
live
vertebrate
embryos.
Our
approach
integrates
optically
guided
situ
subcellular
capillary
microsampling,
one-pot
extraction-digestion
collected
proteins,
peptide
separation
electrophoresis,
ionization
an
ultrasensitive
electrokinetically
pumped
nanoelectrospray,
and
detection
high-resolution
MS
(Orbitrap).
With
a
700
zmol
(420
000
copies)
lower
limit
detection,
this
trace-sensitive
technology
confidently
identified
quantified
∼750-800
protein
groups
(<1%
false-discovery
rate)
analyzing
just
∼5
ng
digest,
viz.
<0.05%
total
content
from
individual
16-cell
Xenopus
laevis
(frog)
embryo.
After
validating
recovering
animal-vegetal-pole
proteomic
asymmetry
frog
zygote,
was
applied
to
uncover
reorganization
as
animal-dorsal
(D11)
embryo
gave
rise
its
neural-tissue-fated
clone
developing
32-,
64-,
128-cell
stages.
In
addition
enabling
on
smaller
X.
laevis,
we
also
demonstrated
be
scalable
zebrafish
Microsampling
raises
exciting
opportunities
study
developmental
processes
whole
organisms
at
level
building
block
life:
cell.
Developmental Cell,
Год журнала:
2021,
Номер
56(10), С. 1541 - 1551.e6
Опубликована: Май 1, 2021
Limb
regeneration,
while
observed
lifelong
in
salamanders,
is
restricted
post-metamorphic
Xenopus
laevis
frogs.
Whether
this
loss
due
to
systemic
factors
or
an
intrinsic
incapability
of
cells
form
competent
stem
has
been
unclear.
Here,
we
use
genetic
fate
mapping
establish
that
connective
tissue
(CT)
the
frog
blastema,
as
case
axolotls.
Using
heterochronic
transplantation
into
limb
bud
and
single-cell
transcriptomic
profiling,
show
axolotl
CT
dedifferentiate
integrate
lineages,
including
cartilage.
In
contrast,
blastema
do
not
fully
re-express
progenitor
program,
even
when
transplanted
bud.
Correspondingly,
contribute
extraskeletal
CT,
but
developing
Furthermore,
using
RNA-seq
analysis
find
embryonic
adult
cartilage
differentiation
programs
are
molecularly
distinct.
This
work
defines
restrictions
dedifferentiation
a
limitation
regeneration.
Partial
phagocytosis-called
trogocytosis-of
axons
by
microglia
has
been
documented
in
ex
vivo
preparations
but
not
directly
observed
vivo.
The
mechanisms
that
modulate
microglial
trogocytosis
of
and
its
function
neural
circuit
development
remain
poorly
understood.
Here,
we
observe
axon
the
developing
Xenopus
laevis
retinotectal
circuit.
We
show
regulate
pruning
retinal
ganglion
cell
are
important
for
proper
behavioral
response
to
dark
bright
looming
stimuli.
Using
bioinformatics,
identify
amphibian
regulator
complement
activation
3,
a
homolog
human
CD46,
as
neuronally
expressed
synapse-associated
inhibitory
molecule
inhibits
axonal
pruning.
membrane-bound
C3
fusion
protein,
demonstrate
enhancing
activity
enhances
Our
results
support
model
remodel
via
neurons
can
control
this
process
through
expression
proteins.