bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Окт. 20, 2023
The
evolutionary
mechanisms
that
drive
the
emergence
of
genome
architecture
remain
poorly
understood
but
can
now
be
assessed
with
unprecedented
power
due
to
massive
accumulation
assemblies
spanning
phylogenetic
diversity.
Transposable
elements
(TEs)
are
a
rich
source
large-effect
mutations
since
they
directly
and
indirectly
genomic
structural
variation
changes
in
gene
expression.
Here,
we
demonstrate
universal
patterns
TE
compartmentalization
across
eukaryotic
genomes
~1.7
billion
years
evolution,
which
TEs
colocalize
families
under
strong
predicted
selective
pressure
for
dynamic
evolution
involved
specific
functions.
For
non-pathogenic
species
these
genes
represent
defense,
sensory
perception
environmental
interaction,
whereas
pathogenic
species,
TE-compartmentalized
highly
enriched
Many
display
signatures
positive
selection
at
molecular
level.
Furthermore,
exhibit
an
excess
high-frequency
alleles
polymorphic
insertions
fruit
fly
populations.
We
postulate
reflect
adaptive
as
well
TE-associated
variants.
This
process
may
shared
diverse
lineages.
Current Opinion in Genetics & Development,
Год журнала:
2023,
Номер
82, С. 102092 - 102092
Опубликована: Июль 28, 2023
Transposable
elements
(TEs)
are
ubiquitous
among
eukaryotic
species.
Their
evolutionary
persistence
is
likely
due
to
a
combination
of
tolerogenic,
evasive/antagonistic,
and
cooperative
interactions
with
their
host
genomes.
Here,
we
focus
on
metazoan
species
review
recent
advances
related
the
harmful
effects
TE
insertions,
including
how
epigenetic
TE-derived
RNAs
can
damage
cells.
We
discuss
new
findings
pathways
that
silence
TEs,
such
as
piRNA
pathway
APOBEC3
Kruppel-associated
box
zinc
finger
gene
families.
Finally,
summarize
novel
strategies
used
by
TEs
evade
silencing,
Y
chromosome
permissive
niche
for
mobilization
counterdefense
block
silencing
factors.
In
this
study,
we
elucidate
the
contribution
of
repetitive
DNA
sequences
to
establishment
social
structures
in
honeybees
(Apis
mellifera).
Despite
recent
advancements
understanding
molecular
mechanisms
underlying
formation
honeybee
castes,
primarily
associated
with
Notch
signaling,
comprehensive
identification
specific
genomic
cis-regulatory
remains
elusive.
Our
objective
is
characterize
landscape
within
genomes
two
subspecies,
namely
A.
m.
mellifera
and
ligustica.
An
observed
burst
repeats
highlights
a
notable
distinction
between
subspecies.
After
that,
transitioned
identifying
differentially
expressed
elements
that
may
function
as
elements.
Nevertheless,
expression
these
showed
minimal
disparity
transcriptome
during
caste
differentiation,
pivotal
process
eusocial
organization.
this,
chromatin
segmentation,
facilitated
by
ATAC-seq,
ChIP-seq,
RNA-seq
data,
revealed
distinct
state
repeats.
Lastly,
an
analysis
sequence
divergence
among
indicates
successive
changes
repeat
states,
correlating
their
respective
time
origin.
Collectively,
findings
propose
potential
role
acquiring
novel
regulatory
functions.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Март 5, 2024
The
structural
organization
of
eukaryotic
genomes
is
contingent
upon
the
fractionation
DNA
into
transcriptionally
permissive
euchromatin
and
repressive
heterochromatin.
However,
we
have
a
limited
understanding
how
these
distinct
states
are
first
established
during
animal
embryogenesis.
Histone
3
lysine
9
trimethylation
(H3K9me3)
critical
to
heterochromatin
formation
bulk
establishment
this
mark
thought
help
drive
large-scale
remodeling
an
initially
naive
chromatin
state
detailed
process
lacking.
Here,
leverage
CUT&RUN
define
emerging
H3K9me3
landscape
zebrafish
embryo
with
high
sensitivity
temporal
resolution.
Despite
prevalence
transposons
in
genome,
found
that
LTR
preferentially
targeted
for
embryonic
deposition,
different
families
exhibiting
timelines.
High
signal-to-noise
ratios
afforded
by
revealed
new,
sites
low-amplitude
initiated
before
major
wave
zygotic
genome
activation
(ZGA).
Early
predominated
at
specific
subsets
were
particularly
enriched
transposon
sequences
maternal
piRNAs
pericentromeric
localization.
Notably,
number
increased
linearly
across
blastula
development,
while
quantitative
comparison
>10-fold
genome-wide
increase
signal
over
just
30
minutes
onset
ZGA.
Continued
maturation
was
observed
beyond
initial
establishment.
Abstract
The
structural
organization
of
eukaryotic
genomes
is
contingent
upon
the
fractionation
DNA
into
transcriptionally
permissive
euchromatin
and
repressive
heterochromatin.
However,
we
have
a
limited
understanding
how
these
distinct
states
are
first
established
during
animal
embryogenesis.
Histone
3
lysine
9
trimethylation
(H3K9me3)
critical
to
heterochromatin
formation,
bulk
establishment
this
mark
thought
help
drive
large-scale
remodeling
an
initially
naive
chromatin
state
detailed
process
lacking.
Here,
leverage
CUT&RUN
define
emerging
H3K9me3
landscape
zebrafish
embryo
with
high
sensitivity
temporal
resolution.
Despite
prevalence
transposons
in
genome,
found
that
LTR
preferentially
targeted
for
embryonic
deposition,
different
families
exhibiting
timelines.
High
signal-to-noise
ratios
afforded
by
revealed
new,
sites
low-amplitude
initiated
before
major
wave
zygotic
genome
activation
(ZGA).
Early
predominated
at
specific
subsets
were
particularly
enriched
transposon
sequences
maternal
piRNAs
pericentromeric
localization.
Notably,
number
increased
linearly
across
blastula
development,
while
quantitative
comparison
>10-fold
genome-wide
increase
signal
over
just
30
min
onset
ZGA.
Continued
maturation
was
observed
beyond
initial
establishment.
PLoS Biology,
Год журнала:
2024,
Номер
22(12), С. e3002887 - e3002887
Опубликована: Дек. 5, 2024
Quality
control
of
translation
is
crucial
for
maintaining
cellular
and
organismal
homeostasis.
Obstacles
in
elongation
induce
ribosome
collision,
which
monitored
by
multiple
sensor
mechanisms
eukaryotes.
The
E3
ubiquitin
ligase
Znf598
recognizes
collided
ribosomes,
triggering
ribosome-associated
quality
(RQC)
to
rescue
stalled
ribosomes
no-go
decay
(NGD)
degrade
stall-prone
mRNAs.
However,
the
impact
RQC
NGD
on
translational
homeostasis
endogenous
mRNAs
has
remained
unclear.
In
this
study,
we
investigated
substrate
during
maternal-to-zygotic
transition
(MZT)
zebrafish
development.
RNA-Seq
analysis
znf598
mutant
embryos
revealed
that
down-regulates
encoding
C2H2-type
zinc
finger
domain
(C2H2-ZF)
MZT.
Reporter
assays
disome
profiling
indicated
stall
collide
while
translating
tandem
C2H2-ZFs,
leading
mRNA
degradation
Znf598.
Our
results
suggest
maintains
translatome
mitigating
risk
collision
at
abundantly
present
C2H2-ZF
sequences
vertebrate
genome.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Дек. 8, 2023
ABSTRACT
Wild
zebrafish
(
Danio
rerio
)
have
a
ZZ/ZW
chromosomal
sex
determination
system
with
the
major
locus
on
right
arm
of
chromosome-4
(Chr4R)
near
largest
heterochromatic
block
in
genome,
suggesting
hypothesis
that
Chr4R
transcriptome
might
be
different
from
rest
genome.
We
conducted
an
RNA-seq
analysis
adult
ZW
ovaries
and
ZZ
testes
identified
four
regions
Chr4
gene
expression
profiles.
Unique
protein-coding
genes
41.7
Mb
section
(Region-2)
were
expressed
testis
but
silent
ovary.
The
AB
lab
strain,
which
lacks
chromosomes,
verified
this
result,
showing
testis-biased
Region-2
depends
gonad
biology,
not
sex-determining
mechanism.
analyses
female
male
brain
liver
validated
few
transcripts
somatic
cells,
without
sex-specificity.
corresponds
to
portion
its
content
repetitive
elements
distinguishes
it
In
Region-2,
lack
human
orthologs;
has
zinc
finger
early
zygotic
genome
activation;
maternal
5S
rRNA
genes,
spliceosome
concentration
tRNA
distinct
set
elements.
colocalization
1)
silenced
are
2)
embryos
briefly
at
onset
3)
maternal-specific
for
translation
machinery;
4)
components;
adjacent
encoding
miR-430,
mediates
transcript
degradation,
suggest
is
Maternal-to-Zygotic-Transition
Gene
Regulatory
Block.
ARTICLE
SUMMARY
wild
chromosome
region,
unique
contains
transiently
embryo
as
begins
express
own
genes.
This
region
also
protein-synthesis
machinery
used
specifically
by
developing
embryos,
molecules
target
degradation
messenger
RNAs
mother
stored
her
eggs.
defines
maternal-to-zygotic-transition
block.
Frontiers in Marine Science,
Год журнала:
2024,
Номер
11
Опубликована: Фев. 28, 2024
Pleuronectiformes
are
flatfishes
with
high
commercial
value
and
a
prominent
example
of
successful
marine
adaptation
through
chromosomal
evolution.
Hence,
the
aim
this
study
was
to
analyze
14
relative
abundance
repetitive
elements
(satellite
DNA
transposable
(TE))
in
15
genome
10
fish
species
(8
flatfish)
delving
into
special
relevance,
16
Senegalese
sole,
Solea
senegalensis.
The
results
showed
differences
elements,
S.
senegalensis
exhibiting
highest
frequency
coverage
these
reaching
40%
not
at
random
distribution.
It
is
noteworthy
presence
relevant
peaks
Helitrons
centromeric/pericentromeric
positions
mainly
bi-armed
chromosomes
1,
2,
4,
6,
7,
9.
position
centromeres
determined
genomic
localization
family
satellite
PvuII
,
other
sequences
obtained
de
novo
.
This
allowed
us
know
19
out
21
an
accumulation
tandem
copies
pericentromeric
1
occupying
region,
first
case,
600Kb
repeats.
That
has
only
been
previously
described
mammals
plants.
Divergence
copy
number
studies
indicated
active
families
species’
existence
two
important
events
transposon
activity
(burst)
senegalensis,
accentuated
Helitrons.
that
transposons
exhibited
landscape
symmetrical
bell-shaped
phylogenetic
analysis
Helitron
revealed
large
groups
four
heterogeneous
distribution
among
chromosomes.
Finally,
phylogenomic
8615
belonging
insertions
from
5
flatfish
external
species,
classify
nine
different
levels
divergence
clusters,
including
some
branches
distant
phylogenetically
species.
implications
will
help
expand
knowledge
chromosome
structure
evolution
medRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Март 15, 2024
Abstract
The
hallmark
of
Chronic
Myeloid
Leukemia
(CML)
is
Philadelphia
chromosome
t(9:22),
which
leads
to
formation
BCR-ABL1
fusion
oncogene.
induces
genetic
instability,
causing
the
progression
chronic
myeloid
leukemia
from
manageable
Phase
(CP-CML)
accelerated
phase
(AP-CML)
and
ultimately
lethal
blast
crisis
(BC-CML).
precise
mechanism
responsible
for
CML
are
not
well
comprehended,
there
a
lack
specific
molecular
biomarkers
advanced
CML.
Mutations
in
transcription
factors
(TFs)
have
significant
role
cancer
initiation,
relapses,
invasion,
metastasis,
resistance
anti-cancer
drugs.
Recently,
our
group
reported
association
novel
factor,
ZNF208,
with
was
dire
need
clinical
validation
this
biomarker.
Therefore,
aim
study
clinically
validate
mutated
ZNF208
as
biomarker
larger
cohort
AP-
BC-CML
patients
using
control-case
studies.
A
total
73
(N=73)
King
Saud
University
Medical
City
Riyadh
Abdulaziz
National
Guard
Hospital,
Al-Ahsa,
Saudi
Arabia
were
enrolled
(2020-2023),
experimental
(cases)
consisting
AP-CML
(n=20)
(n=12).
controls
consisted
age/sex
matched
CP-CML
(n=41).
approved
by
Research
Ethics
Committees
participating
institutes
all
provided
informed
consent
study.
Clinical
evaluations
conducted
according
guidelines
established
European
LeukemiaNet
2020.
Targeted
resequencing
ZNF
208
employed
Illumina
NextSeq500
instrument
(Illumina,
San
Diego,
CA,
USA)
mutations
confirmed
Sanger
sequencing.
Both
next
generation
sequencing
identified
missense
mutation
(c.64G>A)
ZNF208.
56
(93.3)
and12
(100)
CP-,
respectively,
while
none
(0%)
or
healthy
genomic
databases
(p=0.0001).
studies
show
that
very
AP-and
patients.
other
such
proteins
may
cause
carcinogenesis
interacting
KAP-1
repressor
silence
many
target
genes
thus
prove
be
drug
targets
well.
we
recommend
carrying
out
prospective
trials
further
its
utilization
decision,
investigating
pathogenesis
investigate
potential
Simple
Summary
type
blood
caused
oncogene,
leading
instability
changes.
This
results
advancement
(CP)
an
(AP)
finally
(BC).
development
known,
dearth
dependable
shared
indicators.
Transcription
class
molecules
that,
when
altered,
significantly
contribute
cancer,
including
has
been
factor
gene
associated
BC-CML.
Here,
carried
targeted
resequencing.
detected
0
(0%),
respectively
(p=0.0001)
demonstrating
high
specificity
shows
progression.
We
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(19), С. 10525 - 10525
Опубликована: Сен. 30, 2024
As
the
most
abundant
class
of
transcription
factors
in
eukaryotes,
C2H2-type
zinc
finger
proteins
(C2H2-ZFPs)
play
critical
roles
various
biological
processes.
Despite
being
extensively
studied
mammals,
C2H2-ZFPs
remain
poorly
characterized
birds.
Recent
accumulation
multi-omics
data
for
chicken
enables
genome-wide
investigation
The
purpose
this
study
is
to
reveal
genomic
occurrence
and
evolutionary
signature
C2H2-ZFPs,
further
depict
their
expression
profiles
across
diverse
tissues.
Here,
we
annotated
301
genome,
which
are
associated
with
different
effector
domains,
including
KRAB,
BTB,
HOMEO,
PHD,
SCAN,
SET.
Among
them,
KRAB-ZFPs
lack
orthologues
mammals
tend
form
clusters
by
duplication,
supporting
fast
evolution
chicken.
We
also
a
unique
previously
unidentified
SCAN-ZFP,
lineage-specific
highly
expressed
ovary
testis.
By
integrating
101
RNA-seq
datasets
32
tissues,
found
that
have
tissue-specific
expression.
Particularly,
74
C2H2-ZFPs—including
27
KRAB-ZFPs—show
blastoderm-enriched
expression,
indicating
association
early
embryo
development.
Overall,
performs
comprehensive
annotation
profiling
C2H2
ZFPs
gives
new
insights
into
potential
function
avian
species.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 6, 2024
Abstract
The
cell
cycle
is
a
fundamental
process
in
eukaryotic
biology
and
accordingly
controlled
by
highly
conserved
core
signaling
cascade.
However,
whether
recently
evolved
proteins
also
influence
this
unclear.
Here,
we
systematically
map
the
of
evolutionarily
recent
transcription
factors
(TFs)
on
human
progression.
We
find
that
genomic
targets
select
young
TFs,
many
which
belong
to
rapidly
evolving
Krüppel-associated
box
(KRAB)
zinc-finger
(KZFP)
family,
exhibit
synchronized
expression.
Systematic
perturbation
studies
reveal
silencing
TFs
disrupts
normal
progression,
experimentally
confirm
for
ZNF519,
simian-restricted
KZFP.
Further,
show
therian-specific
KZFP
ZNF274
sets
expression
replication
timing
hundreds
clustered
genes.
These
findings
highlight
an
underappreciated
level
lineage
specificity
regulation.