bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2022,
Номер
unknown
Опубликована: Фев. 28, 2022
Abstract
Modern
humans
exhibit
phenotypic
traits
that
are
shared
across
independent
domestication
events,
suggesting
the
human
self-domestication
hypothesis.
Epigenetic
changes
may
facilitate
early
in
humans,
since
they
can
be
first
layer
of
response
to
a
novel
environment.
Here,
we
argue
fish
provide
model
systems
study
epigenetic
drivers
self-domestication.
To
do
this,
compare
genes
carry
domesticates
European
sea
bass
with
1)
anatomically
modern
and
2)
neurodevelopmental
cognitive
disorders
abnormal
traits,
i.e.,
schizophrenia,
Williams
syndrome
autism
spectrum
disorders.
We
found
vs
ancient
were
involved
processes
like
limb
morphogenesis
phenotypes
snout
morphology
hypopigmentation.
Moreover,
impairment
affected
paralogue
such
as
neural
crest
differentiation
ectoderm
differentiation.
conclude
parallel
occur
at
initial
steps
absence
deliberate
selection
phylogenetically
distant
vertebrates.
These
findings
pave
way
for
future
studies
using
models
investigate
human-self
triggers
Genes,
Год журнала:
2022,
Номер
13(6), С. 987 - 987
Опубликована: Май 31, 2022
Modern
humans
exhibit
phenotypic
traits
and
molecular
events
shared
with
other
domesticates
that
are
thought
to
be
by-products
of
selection
for
reduced
aggression.
This
is
the
human
self-domestication
hypothesis.
As
one
first
types
responses
a
novel
environment,
epigenetic
changes
may
have
also
facilitated
early
in
humans.
Here,
we
argue
fish
species,
which
been
recently
domesticated,
can
provide
model
systems
study
drivers
self-domestication.
To
test
this,
used
silico
approaches
compare
genes
European
sea
bass
exhibiting
methylation
anatomically
modern
(comparison
1),
neurodevelopmental
cognitive
disorders
considered
abnormal
traits,
i.e.,
schizophrenia,
Williams
syndrome,
autism
spectrum
2).
Overlapping
comparison
1
were
involved
processes
like
limb
morphogenesis
phenotypes
jaw
morphology
hypopigmentation.
2
affected
paralogue
such
as
neural
crest
differentiation
ectoderm
differentiation.
These
findings
pave
way
future
studies
using
species
models
investigate
triggers
disorders.
Disease Models & Mechanisms,
Год журнала:
2022,
Номер
15(9)
Опубликована: Сен. 1, 2022
Model
organism
(MO)
research
provides
a
basic
understanding
of
biology
and
disease
due
to
the
evolutionary
conservation
molecular
cellular
language
life.
MOs
have
been
used
identify
understand
function
orthologous
genes,
proteins,
cells
tissues
involved
in
biological
processes,
develop
evaluate
techniques
methods,
perform
whole-organism-based
chemical
screens
test
drug
efficacy
toxicity.
However,
growing
richness
datasets
rising
power
computation
raise
an
important
question:
How
do
we
maximize
value
MOs?
In-depth
discussions
over
50
virtual
presentations
organized
by
National
Institutes
Health
across
more
than
10
weeks
yielded
suggestions
for
improving
rigor,
validation,
reproducibility
translatability
MO
research.
The
effort
clarified
challenges
opportunities
developing
integrating
tools
resources.
Maintenance
critical
existing
infrastructure
implementation
suggested
improvements
will
play
roles
maintaining
productivity
facilitating
validation
animal
models
human
disease.
Molecular Biology and Evolution,
Год журнала:
2023,
Номер
40(11)
Опубликована: Окт. 25, 2023
Expression
of
multiple
hemoglobin
isoforms
with
differing
physiochemical
properties
likely
helps
species
adapt
to
different
environmental
and
physiological
conditions.
Antarctic
notothenioid
fishes
inhabit
the
icy
Southern
Ocean
display
fewer
isoforms,
each
less
affinity
for
oxygen
than
temperate
relatives.
Reduced
multiplicity
was
proposed
result
from
relaxed
selective
pressure
in
cold,
thermally
stable,
highly
oxygenated
waters.
These
conditions
also
permitted
survival
diversification
white-blooded
icefishes,
only
vertebrates
living
without
hemoglobin.
To
understand
evolution
during
adaptation
freezing
water,
we
analyzed
genes
36
genome
assemblies.
Results
showed
that
frigid
shaped
gene
by
episodic
diversifying
selection
concomitant
cold
pervasive
notothenioids
compared
relatives,
a
continuing
Analysis
expression
adult
hematopoietic
organs
various
further
revealed
switch
underlying
reduction
fish,
leading
single
isoform
plunderfishes
dragonfishes,
sister
groups
icefishes.
The
predicted
high
fish
embryos
based
on
transcriptomic
data,
however,
raises
questions
about
molecular
bases
implications
diverse
adults.
This
analysis
supports
hypothesis
last
common
icefish
ancestor
vulnerable
detrimental
mutations
affecting
ancestral
expressed
alpha-
beta-globin
pair,
potentially
predisposing
their
subsequent
loss.
Zootaxa,
Год журнала:
2024,
Номер
5501(2), С. 265 - 290
Опубликована: Авг. 29, 2024
Bathydraconidae
(Notothenioidei)
are
a
group
of
benthic
fishes
endemic
to
the
Southern
Ocean.
Because
their
recent
evolutionary
radiation
and
limited
sampling
efforts
due
occurrence
in
remote
regions,
diversity
is
likely
underestimated.
Akarotaxis
nudiceps,
currently
only
recognized
member
its
genus,
an
especially
poorly
known
bathydraconid.
Although
A.
nudiceps
has
circumpolar
distribution
on
Antarctic
continental
shelf,
deep
habitat
rarity
limit
knowledge
life
history
biology.
Using
combination
morphological
genetic
analyses,
we
identified
undescribed
species
this
herein
named
gouldae
sp.
nov.
(Banded
Dragonfish).
The
separation
was
initially
from
archived
larval
specimens,
highlighting
importance
early
stage
taxonomy
natural
collections.
All
adult
specimens
have
been
collected
restricted
~400
km
coastal
section
western
Peninsula,
although
possibly
bias.
This
region
targeted
by
epipelagic
krill
fishery,
which
could
potentially
capture
as
bycatch.
Due
extremely
low
fecundity
near-surface
larvae,
suggest
growing
fishery
negatively
impact
speces.
Journal of Anatomy,
Год журнала:
2021,
Номер
240(1), С. 34 - 49
Опубликована: Авг. 22, 2021
Abstract
Ancestors
of
the
Antarctic
icefishes
(family
Channichthyidae)
were
benthic
and
had
no
swim
bladder,
making
it
energetically
expensive
to
rise
from
ocean
floor.
To
exploit
water
column,
benthopelagic
hypothesized
have
evolved
a
skeleton
with
“reduced
bone,”
which
gross
anatomical
data
supported.
Here,
we
tested
hypothesis
that
changes
icefish
bones
also
occurred
below
level
anatomy.
Histology
micro‐CT
imaging
representative
craniofacial
(i.e.,
ceratohyal,
frontal,
dentary,
articular)
extant
fish
species
specifically
evaluated
two
features
might
cause
appearance
bone”:
bone
microstructure
(e.g.,
volume
fraction
structure
linear
density)
mineral
density
(BMD,
or
mass
per
bone).
Measures
not
consistently
different
in
Chaenocephalus
aceratus
Champsocephalus
gunnari
,
compared
related
notothenioids
Notothenia
coriiceps
Gobionotothen
gibberifrons
.
Some
quantitative
measures,
such
as
density,
significantly
increased
some
homologous
non‐icefish.
However,
differences
rare,
microstructural
measures
across
all
analyzed.
Furthermore,
BMD
was
similar
among
non‐icefish
notothenioids.
In
summary,
bone”
due
systemic
BMD,
raising
prospect
occurs
only
at
anatomic
smaller
fewer
bones).
Given
exhibit
delayed
skeletal
development
fishes,
combining
these
phenotypic
genomic
clarify
genetic
driving
heterochrony.
iScience,
Год журнала:
2022,
Номер
25(7), С. 104588 - 104588
Опубликована: Июнь 15, 2022
Climate
changes
can
promote
disease
outbreaks,
but
their
nature
and
potential
impacts
in
remote
areas
have
received
little
attention.
In
a
hot
spot
of
biodiversity
on
the
West
Antarctic
Peninsula,
which
faces
among
fastest
changing
climates
Earth,
we
captured
specimens
two
notothenioid
fish
species
affected
by
large
skin
tumors
at
an
incidence
never
before
observed
Southern
Ocean.
Molecular
histopathological
analyses
revealed
that
X-cell
parasitic
alveolates,
members
genus
call
Notoxcellia,
are
etiological
agent
these
tumors.
Parasite-specific
molecular
probes
showed
xenomas
remained
within
largely
outgrew
host
cells
dermis.
We
further
induced
neovascularization
underlying
tissue
detrimentally
growth
condition.
Although
many
knowledge
gaps
persist
about
disease,
including
its
mode
transmission
life
cycle,
findings
reveal
potentially
active
biotic
threats
to
vulnerable
ecosystems.
Frontiers in Genetics,
Год журнала:
2022,
Номер
13
Опубликована: Сен. 8, 2022
Mitochondrial
DNA
is
primarily
maternally
inherited
in
most
animals
and
evolves
about
10
times
faster
than
biparentally
nuclear
DNA.
dysfunction
(mt-dys)
arises
when
interactions
between
the
co-evolving
mitochondrial
genomes
are
perturbed
essential
processes
like
oxidative
phosphorylation
(OXPHOS).
Over
time
mt-dys
can
lead
to
diseases
(mt-diseases),
which
surprisingly
prevalent
include
common
such
as
Alzheimer's,
Parkinson's,
diabetes.
Unfortunately,
strong
impact
that
intraspecific
genetic
variation
has
on
mt-disease
complicates
its
study
development
of
effective
treatments.
Animal
models
have
advanced
our
understanding
but
their
relevance
human
conditions
often
limited
by
relatively
low
diversity.
Many
traditional
laboratory
also
typically
a
single
haplotype
(mitotype),
stark
contrast
over
5,000
mitotypes
humans
worldwide.
The
threespine
stickleback
fish
an
evolutionary
history
made
it
favorable
mutant
model
(EMM)
for
studying
mito-nuclear
possibly
mt-diseases.
EMMs
species
with
naturally
evolved
states
mimic
maladaptive
diseases.
In
stickleback,
period
isolation
followed
introgression
genome
from
sister
resulted
maintenance
two
distinct
haplotypes
continue
segregate
within
many
populations
wild
stickleback.
existence
mitogenomes
segregating
numerous
genetically
diverse
provides
unique
system
exploring
complex
dynamics.
Here
we
provide
first
complete
coding
region
analysis
mitotypes,
whose
mitogenomic
divergence
exceeds
other
mammalian
disease
even
ancient
modern
humans.
We
find
not
uniform
across
mitogenome,
impacts
protein
genes,
significantly
proteins
Complex
I
OXPHOS.
full
characterization
these
highly
divergent
foundation
EMM
interactions.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2022,
Номер
unknown
Опубликована: Сен. 20, 2022
Abstract
Mitochondrial
genomes
are
known
for
their
compact
size
and
conserved
gene
order,
however,
recent
studies
employing
long-read
sequencing
technologies
have
revealed
the
presence
of
atypical
mitogenomes
in
some
species.
In
this
study,
we
assembled
annotated
five
Antarctic
notothenioids,
including
four
icefishes
(
Champsocephalus
gunnari,
C.
esox,
Chaenocephalus
aceratus
,
Pseudochaenuchthys
georgianus
)
cold-specialized
Trematomus
borchgrevinki
.
notothenioids
to
harbor
rearrangements
mt
genomes,
however
extensive
duplications
observed
our
study
never
been
reported
before.
icefishes,
protein
coding
ND6
two
transfer
RNAs,
control
region
with
different
copy
number
variants
present
within
same
individuals
appearing
follow
canonical
Duplication-Degeneration-Complementation
(DDC)
model
esox
gunnari
addition,
using
k-mer
analysis,
were
able
detect
heteroplasmy
We
also
a
large
inversion
mitogenome
T.
along
tandem
repeats
its
region.
This
is
first
assemble
identify
structural
notothenioid
signifies
importance
long-reads
resolving
complex
mitochondrial
architectures.
Identification
such
wide-ranging
these
fishes
could
provide
insight
into
genetic
basis
icefish
physiology
more
generally
may
insights
about
potential
role
cold
adaptation.