Genome Biology and Evolution,
Journal Year:
2020,
Volume and Issue:
unknown
Published: Oct. 9, 2020
The
role
of
sex-specific
demography
in
hybridization
and
admixture
genetically
diverged
species
populations
is
essential
to
understand
the
origins
genomic
diversity
sexually
reproducing
organisms.
In
order
infer
how
sex-linked
loci
have
been
differentiated
undergoing
frequent
admixture,
we
examined
17
whole-genome
sequences
seven
representing
genus
Macaca,
which
shows
inter-specific
predominantly
female
philopatry.
We
found
that
were
prevalent
within
these
species.
For
three
cases
suggested
hybrid
origin
species/subspecies,
Macaca
arctoides,
fascicularis
ssp.
aurea,
Chinese
mulatta,
level
X
chromosomes,
less
affected
by
male-biased
migration
than
autosomes.
one
case,
cyclopis
fuscata
was
closer
M.
mulatta
Indian
fuscata/cyclopis
more
pronounced
on
chromosome
Since
mitochondrial
genomes
cyclopis,
cluster
together,
genome
distantly
related,
observed
pattern
genetic
differentiation
X-chromosomal
consistent
with
nuclear
swamping
hypothesis,
strong,
continuous
introgression
from
ancestral
population
a
related
generated
incongruencies
between
genealogies
genomes.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Feb. 28, 2024
Abstract
Biological
invasions
are
a
major
threat
to
biodiversity.
Therefore,
monitoring
genomic
features
of
invasive
species
is
crucial
understand
their
population
structure
and
adaptive
processes.
However,
resources
scarce,
compromising
the
study
success.
Here,
we
present
reference
genome
Styela
plicata
,
one
most
widespread
marine
species,
combined
with
data
24
individuals
from
6
populations
distributed
worldwide.
We
characterized
large
inversions
in
four
chromosomes,
accounting
for
~
15%
size.
These
polymorphic
through
species’
distribution
area,
enriched
genes
enhancing
fitness
estuary
harbor
environments.
Nonetheless,
mask
detection
S.
structure.
When
these
structural
variants
removed,
successfully
identify
main
oceanographic
barriers
accurately
characterize
differentiation
between
within
ocean
basins.
Several
located
chromosome
3
showcased
as
drivers
biogeographic
regions.
Moreover,
recover
three
mitogenomic
clades,
involving
rearrangements
leading
cyto-nuclear
coevolution
likely
involved
mitochondrion
during
cell
division.
Our
results
suggest
that
contribute
structuring
adaptation
processes,
potentially
success
when
colonizing
new
habitats.
Molecular Biology and Evolution,
Journal Year:
2022,
Volume and Issue:
39(11)
Published: Oct. 27, 2022
Abstract
Mitochondrial
(mt)
and
nuclear-encoded
proteins
are
integrated
in
aerobic
respiration,
requiring
co-functionality
among
gene
products
from
fundamentally
different
genomes.
Different
evolutionary
rates,
inheritance
mechanisms,
selection
pressures
set
the
stage
for
incompatibilities
between
interacting
of
two
The
mitonuclear
coevolution
hypothesis
posits
that
may
be
avoided
if
evolution
one
genome
selects
complementary
changes
genes
encoded
by
other
genome.
Nuclear
compensation,
which
deleterious
mtDNA
offset
compensatory
nuclear
changes,
is
often
invoked
as
primary
mechanism
coevolution.
Yet,
direct
evidence
supporting
compensation
rare.
Here,
we
used
data
58
mammalian
species
representing
eight
orders
to
show
strong
correlations
rates
mt
mt-targeted
(N-mt)
proteins,
but
not
non-mt-targeted
providing
support
across
mammals.
N-mt
with
interactions
also
showed
strongest
correlations.
Although
most
had
elevated
dN/dS
ratios
compared
(as
predicted
under
compensation),
sites
close
contact
were
overrepresented
signs
positive
noncontact
(contrary
predictions
compensation).
Furthermore,
temporal
patterns
amino
acid
substitutions
did
even
positively
selected,
functionally
important
residues
contacts.
Overall,
our
results
strongly
∼170
million
years
fail
major
mode
Molecular Biology and Evolution,
Journal Year:
2024,
Volume and Issue:
41(3)
Published: Feb. 23, 2024
Abstract
The
interaction
and
coevolution
between
nuclear
cytoplasmic
genomes
are
one
of
the
fundamental
hallmarks
eukaryotic
genome
evolution
and,
2
billion
yr
later,
still
major
contributors
to
formation
new
species.
Although
many
studies
have
investigated
role
cytonuclear
interactions
following
allopolyploidization,
relative
magnitude
effect
subgenome
dominance
versus
on
remains
unclear.
Brassica
triangle
U
features
3
diploid
species
that
together
formed
separate
allotetraploid
similar
evolutionary
timescales,
providing
an
ideal
system
for
understanding
contribution
donor
hybrid
polyploid.
Here,
we
pattern
organelle-targeted
genes
in
carinata
(BBCC)
varieties
juncea
(AABB)
at
whole-genome
level,
with
particular
focus
enzyme
complexes.
We
found
partial
evidence
plastid-targeted
experience
selection
match
plastid
genomes,
but
no
obvious
corresponding
signal
mitochondria-targeted
from
these
separately
allopolyploids.
Interestingly,
acting
always
reduced
retention
rate
encoded
by
B
subgenome,
regardless
whether
nigra
(BB)
was
contributed
paternal
or
maternal
progenitor.
More
broadly,
this
study
illustrates
distinct
selective
pressures
experienced
plastid-
genes,
despite
a
shared
inheritance
natural
history.
Our
also
highlights
important
allopolyploid
evolution,
even
whose
function
depends
inherited
molecules.
Molecular Ecology,
Journal Year:
2024,
Volume and Issue:
33(12)
Published: May 10, 2024
Abstract
Understanding
genetic
incompatibilities
and
introgression
between
incipient
species
are
major
goals
in
evolutionary
biology.
Mitochondrial
genes
evolve
rapidly
exist
dense
gene
networks
with
coevolved
nuclear
genes,
suggesting
that
mitochondrial
respiration
may
be
particularly
susceptible
to
disruption
hybrid
organisms.
Mitonuclear
interactions
have
been
demonstrated
contribute
dysfunction
deeply
divergent
taxa
crossed
the
laboratory,
but
there
few
empirical
examples
of
mitonuclear
younger
lineages
naturally
hybridize.
Here,
we
use
controlled
crosses
high‐resolution
respirometry
provide
first
experimental
evidence
a
bird
inter‐lineage
impact
aerobic
metabolism.
Specifically,
capacity
two
mitodiscordant
backcrosses
(with
mismatched
combinations)
differs
from
one
another,
although
they
do
not
differ
significantly
parental
groups
or
mitoconcordant
as
would
expect
disruptions.
In
wild
zone
these
subspecies,
cline
centre
is
shifted
west
centre,
which
consistent
direction
our
results.
Our
results
therefore
demonstrate
asymmetric
cellular
help
explain
geographic
discordance
genomes
observed
wild.
Evolution Letters,
Journal Year:
2024,
Volume and Issue:
8(6), P. 916 - 926
Published: Aug. 9, 2024
Abstract
Mitochondrial
function
depends
on
the
effective
interactions
between
proteins
and
RNA
encoded
by
mitochondrial
nuclear
genomes.
Evidence
suggests
that
both
genomes
respond
to
thermal
selection
promote
adaptation.
However,
contribution
of
their
epistatic
life
history
phenotypes
in
wild
remains
elusive.
We
investigated
evolutionary
implications
mitonuclear
a
real-world
scenario
sees
populations
adapted
different
environments,
altering
geographical
distribution
while
experiencing
flow
admixture.
created
Drosophila
melanogaster
panel
with
replicate
native
from
ends
Australian
east-coast
cline,
into
which
we
substituted
mtDNA
haplotypes
were
either
predominant
or
rare
at
each
cline-end,
thus
creating
putatively
matched
mismatched
populations.
Our
results
suggest
mismatching
may
impact
phenotype,
harboring
rarer
haplotype
suffering
trade-off
aerobic
capacity
key
fitness
aspects
such
as
reproduction,
growth,
survival.
discuss
significance
modulators
context
future
adaptation
population
persistence.
Journal of Inherited Metabolic Disease,
Journal Year:
2020,
Volume and Issue:
44(2), P. 325 - 342
Published: Oct. 25, 2020
Abstract
Mitochondrial
disorders
make
up
a
large
class
of
heritable
diseases
that
cause
broad
array
different
human
pathologies.
They
can
affect
many
organ
systems,
or
display
very
specific
tissue
presentation,
and
lead
to
illness
either
in
childhood
later
life.
While
the
over
1200
genes
encoded
nuclear
DNA
play
an
important
role
mitochondrial
disease,
it
has
been
known
for
30
years
mutations
mitochondria's
own
small,
multicopy
chromosome
(mtDNA)
diseases.
Unfortunately,
animal
mtDNA
resisted
transgenic
directed
genome
editing
technologies
until
quite
recently.
As
such,
models
aid
our
understanding
these
diseases,
explore
preclinical
therapeutic
research
have
rare.
This
review
will
discuss
unusual
properties
mitochondria
hindered
generation
models.
It
also
existing
mammalian
describe
methods
employed
their
generation,
recent
advances
targeting
DNA‐manipulating
enzymes
how
may
be
generate
new
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2021,
Volume and Issue:
unknown
Published: July 14, 2021
Abstract
The
evolution
of
reproductive
barriers
is
the
first
step
in
formation
new
species
and
can
help
us
understand
diversification
life
on
Earth.
These
often
take
form
“hybrid
incompatibilities,”
where
alleles
derived
from
two
different
no
longer
interact
properly
hybrids.
Theory
predicts
that
hybrid
incompatibilities
may
be
more
likely
to
arise
at
rapidly
evolving
genes
involving
multiple
should
common,
but
there
has
been
sparse
empirical
data
evaluate
these
predictions.
Here,
we
describe
a
mitonuclear
incompatibility
three
physical
contact
within
respiratory
Complex
I
naturally
hybridizing
swordtail
fish
species.
Individuals
homozygous
for
specific
mismatched
protein
combinations
fail
complete
embryonic
development
or
die
as
juveniles,
while
those
heterozygous
have
reduced
function
unbalanced
representation
parental
mitochondrial
proteome.
We
find
impacts
genetic
interactions
survival
are
non-additive,
highlighting
subtle
complexity
architecture
incompatibilities.
document
evolutionary
history
involved,
showing
time
an
transferred
between
via
hybridization.
This
work
thus
provides
glimpse
into
architecture,
physiological
impacts,
origin
complex
impacting
Genome Research,
Journal Year:
2021,
Volume and Issue:
31(7), P. 1203 - 1215
Published: May 4, 2021
In
contrast
to
the
western
honey
bee,
Apis
mellifera,
other
bee
species
have
been
largely
neglected
despite
their
importance
and
diversity.
The
genetic
basis
of
evolutionary
diversification
bees
remains
unknown.
Here,
we
provide
a
genome-wide
comparison
three
species,
each
representing
one
subgenera
bees,
namely
dwarf
(Apis
florea),
giant
(A.
dorsata),
cavity-nesting
mellifera)
with
bumblebees
as
an
outgroup.
Our
analyses
resolve
phylogeny
diverging
first.
We
find
that
evolution
increased
eusocial
complexity
in
proceeds
via
increases
gene
regulation,
which
is
agreement
previous
studies.
However,
this
process
seems
be
related
pathways
than
transcriptional
control.
Positive
selection
patterns
across
reveal
trade-off
between
maintaining
genome
stability
generating
diversity,
rapidly
evolving
piRNA
pathway
leading
genomes
depleted
transposable
elements,
DNA
repair
associated
high
recombination
rates
all
species.
Diversification
within
accompanied
by
positive
several
genes
whose
putative
functions
present
candidate
mechanisms
for
lineage-specific
adaptations,
such
migration,
immunity,
nesting
behavior.
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: Aug. 30, 2022
Abstract
Human
mitochondrial
gene
expression
relies
on
the
specific
recognition
and
aminoacylation
of
tRNAs
(mtRNAs)
by
nuclear-encoded
aminoacyl-tRNA
synthetases
(mt-aaRSs).
Despite
their
essential
role
in
cellular
energy
homeostasis,
strong
mutation
pressure
genetic
drift
have
led
to
an
unparalleled
sequence
erosion
animal
mtRNAs.
The
structural
functional
consequences
this
are
not
understood.
Here,
we
present
cryo-EM
structures
human
seryl-tRNA
synthetase
(mSerRS)
complex
with
mtRNA
Ser(GCU)
.
These
reveal
a
unique
mechanism
substrate
aminoacylation.
is
highly
degenerated,
having
lost
entire
D-arm,
tertiary
core,
stable
L-shaped
fold
that
define
canonical
tRNAs.
Instead,
evolved
innovations,
including
radically
altered
T-arm
topology
serves
as
critical
identity
determinant
unusual
shape-selective
readout
mSerRS.
Our
results
provide
molecular
framework
understand
principles
mito-nuclear
co-evolution
specialized
mechanisms
tRNA
mammalian
expression.