bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2022,
Номер
unknown
Опубликована: Май 9, 2022
SUMMARY
RNA
interference
systems
depend
on
the
synthesis
of
small
precursors
whose
sequences
define
target
spectrum
these
silencing
pathways.
The
Drosophila
Heterochromatin
Protein
1
(HP1)
variant
Rhino
permits
transcription
PIWI-interacting
(piRNA)
within
transposon-rich
heterochromatic
loci
in
germline
cells.
Current
models
propose
that
Rhino’s
specific
chromatin
occupancy
at
piRNA
source
is
determined
by
histone
marks
and
maternally
inherited
piRNAs,
but
also
imply
existence
other,
undiscovered
specificity
cues.
Here,
we
identify
a
member
diverse
family
zinc
finger
associated
domain
(ZAD)-C
2
H
proteins,
Kipferl,
as
critical
cofactor
ovaries.
By
binding
to
guanosine-rich
DNA
motifs
interacting
with
chromodomain,
Kipferl
recruits
stabilizes
it
chromatin.
In
kipferl
mutant
flies,
lost
from
most
its
instead
accumulates
pericentromeric
satellite
arrays,
resulting
decreased
levels
transposon
targeting
piRNAs
impaired
fertility.
Our
findings
reveal
sequence,
addition
H3K9me3
mark,
determines
identity
provide
insight
into
how
might
be
caught
crossfire
genetic
conflicts.
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.
Annual Review of Genetics,
Год журнала:
2021,
Номер
55(1), С. 401 - 425
Опубликована: Ноя. 23, 2021
Repeat-enriched
genomic
regions
evolve
rapidly
and
yet
support
strictly
conserved
functions
like
faithful
chromosome
transmission
the
preservation
of
genome
integrity.
The
leading
resolution
to
this
paradox
is
that
DNA
repeat–packaging
proteins
adaptively
mitigate
deleterious
changes
in
repeat
copy
number,
sequence,
organization.
Exciting
new
research
has
tested
model
coevolution
by
engineering
evolutionary
mismatches
between
evolving
chromatin
one
species
repeats
a
close
relative.
Here,
we
review
these
innovative
evolution-guided
functional
analyses.
studies
demonstrate
vital,
chromatin-mediated
cellular
processes,
including
transposon
suppression,
transmission,
retention
depend
on
species-specific
versions
package
repeats.
In
many
cases,
ever-evolving
are
selfish
genetic
elements,
raising
possibility
battleground
intragenomic
conflict.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Ноя. 15, 2023
New
genes
(or
young
genes)
are
genetic
novelties
pivotal
in
mammalian
evolution.
However,
their
phenotypic
impacts
and
evolutionary
patterns
over
time
remain
elusive
humans
due
to
the
technical
ethical
complexities
of
functional
studies.
Integrating
gene
age
dating
with
Mendelian
disease
phenotyping,
our
research
shows
a
gradual
rise
proportion
as
increases.
Logistic
regression
modeling
indicates
that
this
increase
older
may
be
related
longer
sequence
lengths
higher
burdens
deleterious
de
novo
germline
variants
(DNVs).
We
also
find
steady
integration
new
biomedical
phenotypes
into
human
genome
macroevolutionary
timescales
(~0.07%
per
million
years).
Despite
stable
pace,
we
observe
distinct
enrichment,
pleiotropy,
selective
pressures
across
ages.
Notably,
show
significant
enrichment
diseases
male
reproductive
system,
indicating
strong
sexual
selection.
Young
exhibit
disease-related
functions
tissues
systems
potentially
linked
innovations,
such
increased
brain
size,
musculoskeletal
phenotypes,
color
vision.
further
reveal
logistic
growth
pattern
pleiotropy
time,
diminishing
marginal
for
intensifying
constraints
time.
propose
"pleiotropy-barrier"
model
delineates
potentials
innovation
compared
genes,
process
is
subject
natural
Our
study
demonstrates
evolutionarily
critical
influencing
evolution
adaptive
innovations
driven
by
selection,
low
advantage.
Molecular Ecology,
Год журнала:
2021,
Номер
30(18), С. 4448 - 4465
Опубликована: Июль 3, 2021
Human
induced
environmental
change
may
require
rapid
adaptation
of
plant
populations
and
crops,
but
the
genomic
basis
remain
poorly
understood.
We
analysed
polymorphic
loci
from
perennial
crop
Medicago
sativa
(alfalfa
or
lucerne)
annual
legume
model
species
M.
truncatula
to
search
for
a
common
set
candidate
genes
that
might
contribute
abiotic
stress
in
both
species.
identified
associated
with
gradients
along
distribution
two
Candidate
each
were
detected
homologous
linkage
blocks
using
genome-environment
(GEA)
genome-phenotype
association
analyses.
Hundreds
GEA
species-specific,
these,
13.4%
(M.
sativa)
24%
truncatula)
also
significantly
phenotypic
traits.
A
168
candidates
shared
by
species,
which
was
25.4%
more
than
expected
chance.
When
combined,
they
explained
high
proportion
variance
certain
traits
adaptation.
Genes
highly
conserved
functions
dominated
among
enriched
gene
ontology
terms
have
shown
play
central
role
drought
avoidance
tolerance
mechanisms
means
cellular
shape
modifications
other
cell
homeostasis.
Our
results
point
existence
molecular
determined
functions.
discuss
these
light
recently
proposed
omnigenic
complex
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Июнь 14, 2024
Summary
From
RNA
interference
to
chromatin
silencing,
diverse
genome
defense
pathways
silence
selfish
genetic
elements
safeguard
integrity
1,2
.
Despite
their
diversity,
different
share
a
modular
organization,
where
numerous
specificity
factors
identify
targets
and
common
effectors
them.
In
the
PIWI-interacting
(piRNA)
pathway,
which
controls
in
metazoan
germline,
target
RNAs
are
first
identified
by
complementary
base
pairing
with
piRNAs
then
silenced
PIWI-clade
nucleases
via
enzymatic
cleavage
1,3
Such
binary
architecture
allows
systems
be
readily
adaptable,
new
can
captured
innovation
of
4,5
Thus,
our
current
understanding
against
lineage-specific
genes
has
been
largely
limited
evolution
factors,
while
it
remains
poorly
understood
whether
other
types
innovations
required.
Here,
we
describe
type
innovation,
escalates
capacity
piRNA
pathway
control
recently
expanded
gene
Drosophila
melanogaster
Through
an
vivo
RNAi
screen
for
repressors
Stellate
—a
evolved
meiotic
driver
6–8
—we
discovered
novel
factor,
Trailblazer.
Trailblazer
is
transcription
factor
that
promotes
expression
two
nucleases,
Aub
AGO3,
match
abundance.
Recent
DNA-binding
domain
enabled
drastically
elevate
AGO3
D.
lineage,
thereby
escalating
silencing
fertility.
As
copy-number
expansion
recurrent
feature
across
tree
life
9–12
,
envision
augmenting
quantitatively
likely
repeatedly
employed
strategy
evolution.
Abstract
The
genome
sequencing
revolution
has
revealed
that
all
species
possess
a
large
number
of
unique
genes
critical
for
trait
variation,
adaptation,
and
evolutionary
innovation.
One
widely
used
approach
to
identify
such
consists
detecting
protein‐coding
sequences
with
no
homology
in
other
genomes,
termed
orphan
genes.
These
have
been
extensively
studied,
under
the
assumption
they
represent
valid
proxies
species‐specific
Here,
we
critically
evaluate
taxonomic,
phylogenetic,
sequence
evolution
evidence
showing
belong
range
ages
thus
cannot
be
assigned
single
lineage.
Furthermore,
show
processes
generating
are
substantially
more
diverse
than
generally
thought
include
horizontal
gene
transfer,
transposable
element
domestication,
overprinting.
Thus,
heterogeneous
collection
rather
biological
entity,
making
them
unsuitable
as
subject
meaningful
investigation
phenotypic