bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2022,
Volume and Issue:
unknown
Published: Oct. 7, 2022
Abstract
Large
regions
of
suppressed
recombination
having
extended
over
time
occur
in
many
organisms
around
genes
involved
mating
compatibility
(sex-determining
or
mating-type
genes).
The
sheltering
deleterious
alleles
has
been
proposed
to
be
such
expansions.
However,
the
dynamics
mutations
partially
linked
are
not
well
understood,
especially
finite
populations.
In
particular,
under
what
conditions
likely
maintained
for
long
enough
near
mating-compatibility
remains
evaluated,
selfing,
which
generally
increases
purging
rate
mutations.
Using
a
branching
process
approximation,
we
studied
fate
new
overdominant
mutation
diploid
population,
considering
locus
carrying
two
permanently
heterozygous
alleles,
and
at
appears.
We
obtained
analytical
numerical
results
on
probability
mutation.
investigated
impact
between
loci
system
(outcrossing,
intra
inter-tetrad
selfing)
maintenance
found
that
presence
fungal-like
(
i.e
.
preventing
always
sheltered
it
decreased
increased
effect
was
higher
case
automixis
(intra-tetrad
selfing).
This
may
contribute
explain
why
evolutionary
strata
suppression
mostly
automictic
(pseudo-homothallic)
fungi.
also
showed
rare
events
during
strikingly
times
could
occur,
suggesting
can
indeed
accumulate
scales.
conclusion,
our
show
that,
although
selfing
purges
mutations,
these
very
locus,
promote
evolution
sex-related
chromosomes.
Annual Review of Animal Biosciences,
Journal Year:
2023,
Volume and Issue:
12(1), P. 233 - 259
Published: Oct. 20, 2023
Sexual
reproduction
is
prevalent
across
diverse
taxa.
However,
sex-determination
mechanisms
are
so
that
even
closely
related
species
often
differ
in
systems.
Teleost
fish
a
taxonomic
group
with
frequent
turnovers
of
sex-determining
and
thus
provides
us
great
opportunities
to
investigate
the
molecular
evolutionary
underlying
turnover
Here,
we
compile
recent
studies
on
diversity
fish.
We
demonstrate
genes
TGF-β
signaling
pathway
frequently
used
for
master
(MSD)
genes.
MSD
arise
via
two
main
mechanisms,
duplication-and-transposition
allelic
mutations,
few
exceptions.
also
temperature
influences
sex
determination
many
species,
those
chromosomes,
higher
temperatures
inducing
differentiation
into
males
most
cases.
Finally,
review
theoretical
models
discuss
what
questions
remain
elusive.
Molecular Ecology,
Journal Year:
2024,
Volume and Issue:
33(24)
Published: Jan. 5, 2024
Sex
chromosomes
play
an
outsized
role
in
adaptation
and
speciation,
thus
deserve
particular
attention
evolutionary
genomics.
In
particular,
fusions
between
sex
autosomes
can
produce
neo-sex
chromosomes,
which
offer
important
insights
into
the
dynamics
of
chromosomes.
Here,
we
investigate
origin
previously
reported
Danaus
chromosome
within
tribe
Danaini.
We
assembled
annotated
genomes
Tirumala
septentrionis
(subtribe
Danaina),
Ideopsis
similis
(Amaurina),
Idea
leuconoe
(Euploeina)
Lycorea
halia
(Itunina)
identified
their
Z-linked
scaffolds.
found
that
resulting
from
fusion
a
Z
autosome
corresponding
to
Melitaea
cinxia
(McChr)
21
arose
common
ancestor
Danaina,
Amaurina
Euploina.
also
two
additional
as
W
further
fused
with
synteny
block
McChr31
I.
independent
occurred
ancestral
McChr12
L.
halia.
tested
possible
sexually
antagonistic
selection
turnover
by
analysing
genomic
distribution
sex-biased
genes
The
McChr21
involved
are
significantly
enriched
female-
male-biased
genes,
respectively,
could
have
hypothetically
facilitated
fixation
This
suggests
sexual
antagonism
Lepidoptera.
neo-Z
both
appear
fully
compensated
somatic
tissues,
but
extent
dosage
compensation
for
varies
across
tissues
species.
Molecular Biology and Evolution,
Journal Year:
2024,
Volume and Issue:
41(11)
Published: Oct. 16, 2024
Abstract
Sex
chromosomes
are
widespread
in
species
with
separate
sexes.
They
have
evolved
many
times
independently
and
display
a
truly
remarkable
diversity.
New
sequencing
technologies
methodological
developments
allowed
the
field
of
molecular
evolution
to
explore
this
diversity
large
number
model
nonmodel
organisms,
broadening
our
vision
on
mechanisms
involved
their
evolution.
Diverse
studies
us
better
capture
common
evolutionary
routes
that
shape
sex
chromosomes;
however,
we
still
mostly
fail
explain
why
so
diverse.
We
review
over
half
century
theoretical
empirical
work
chromosome
highlight
pending
questions
origins,
turnovers,
rearrangements,
degeneration,
dosage
compensation,
gene
content,
rates
also
report
recent
progress
understanding
ultimate
reasons
for
chromosomes’
existence.
Philosophical Transactions of the Royal Society B Biological Sciences,
Journal Year:
2022,
Volume and Issue:
377(1856)
Published: June 13, 2022
Supergenes
are
tightly
linked
sets
of
loci
that
inherited
together
and
control
complex
phenotypes.
While
classical
supergenes-governing
traits
such
as
wing
patterns
in
Heliconius
butterflies
or
heterostyly
Primula-have
been
studied
since
the
Modern
Synthesis,
we
still
understand
very
little
about
how
they
evolve
persist
nature.
The
genetic
architecture
supergenes
is
a
critical
factor
affecting
their
evolutionary
fate,
it
can
change
key
parameters
recombination
rate
effective
population
size,
potentially
redirecting
molecular
evolution
supergene
addition
to
surrounding
genomic
region.
To
evolution,
must
link
with
processes.
This
now
becoming
possible
recent
advances
sequencing
technology
powerful
forward
computer
simulations.
present
theme
issue
brings
theoretical
empirical
papers,
well
opinion
synthesis
which
showcase
architectural
diversity
connect
this
processes
polymorphism
maintenance
mutation
accumulation.
Here,
summarize
those
insights
highlight
new
ideas
methods
illuminate
path
for
study
article
part
'Genomic
supergenes:
causes
consequences'.
Philosophical Transactions of the Royal Society B Biological Sciences,
Journal Year:
2022,
Volume and Issue:
377(1856)
Published: June 13, 2022
Intralocus
sexually
antagonistic
selection
occurs
when
an
allele
is
beneficial
to
one
sex
but
detrimental
the
other.
This
form
of
thought
be
key
evolution
chromosomes
hard
detect.
Here
we
perform
analysis
phased
young
look
for
signals
in
Japan
Sea
stickleback
(Gasterosteus
nipponicus).
Phasing
allows
us
date
suppression
recombination
on
chromosome
and
provides
unprecedented
resolution
identify
recombining
region
chromosome.
We
four
windows
with
elevated
divergence
between
X
Y
region,
all
or
very
near
genes
associated
phenotypes
potentially
under
humans.
are
unable,
however,
rule
out
alternative
hypothesis
that
peaks
result
from
demographic
effects.
Thus,
although
a
formation
supergenes
chromosomes,
it
remains
challenging
article
part
theme
issue
'Genomic
architecture
supergenes:
causes
evolutionary
consequences'.
Journal of Evolutionary Biology,
Journal Year:
2023,
Volume and Issue:
36(3), P. 632 - 636
Published: Jan. 22, 2023
Sex
chromosomes
either
carry
a
factor
like
the
male-determining
factors
of
mammals
(Berta
et
al.,
1990)
or
plant
Silene
latifolia
(Westergaard,
1958),
function
in
balanced
sex-determining
systems,
as
Drosophila
(Bridges,
1925)
and
Caenorhabditis
elegans
(Meyer,
2022).
The
sex
chromosome
pairs
these
several
other
species
include
physically
extensive
fully
Y-linked,
male-specific,
regions
('MSY')
that
have
undergone
'genetic
degeneration'
lost
most
genes
are
carried
on
X
(X-linked
then
hemizygous
males).
Similar
losses
recombination,
similar
degeneration,
occurred
evolution
with
female
heterogamety,
including
birds
Lepidoptera,
respectively,
reviewed
by
Wang
al.
(2014)
Fraisse
(2017).
lack
recombination
is
probably
not
direct
consequence
carrying
genes,
having
an
essential
role
determination,
since
unrelated
fish
small
located
within
recombining
(Koyama
2019;
Kuhl
2021;
Nacif
2022;
Reichwald
2015),
completely
sex-linked
some
plants
smaller
than
1
Mb
(Akagi
2014;
Harkess
2020).
These
situations
can
be
explained
ways,
for
example
they
could
reflect
recent
separate
sexes,
appearance
genome
region
so-called
turnover
event
(Vicoso,
2019).
Species
whose
pair
has
changes
which
formerly
stopped
previously
established
therefore
important,
because
tell
us
became
suppressed
after
their
locus
evolved.
first
case
to
discovered
was
Eutherian
mammals.
earliest
enlargement
MSY
involved
fusion
Y
chromosome,
autosome
Marsupials
(Waters
2001).
This
around
115
million
years
ago
(Cortez
2014).
Further
enlargements
caused
subsequent
suppression
events
produced
'evolutionary
strata'
wide
differences
sequence
divergence
between
Y-X
different
(Figure
1).
Based
genetic
map
estimated
females
(which
represents
ancestral
order
added
chromosome),
recently
near
still
recombines,
pseudo-autosomal
region,
'PAR'
(Lahn
&
Page,
1999;
Skaletsky
2003).
In
two
evolved
strata
humans,
median
synonymous
site
values
14%
26%,
almost
high
rest
(Sayres
Makova,
2013).
Very
varied
divergence,
perhaps
reflecting
strata,
also
seen
latifolia,
carnation
family
(Bergero
2007;
Papadopulos
2015).
threespine
stickleback,
without
fusions
any
autosomes,
shows
clear
Figure
1b
(Peichel
2020),
been
inferred
ZW
Neognathous
(Wang
A
may
always
such
(Charlesworth,
However,
cases
when
(shrinking
PAR
changing
its
boundary
region)
demand
explanation.
Several
hypotheses
proposed.
One
idea
sexually
antagonistic
polymorphisms
become
(e.g.
male-benefit
allele
would
reduce
fitness
more
likely
spread
if
closely
linked
one
same
effects
autosomal).
Should
mutation
establish
polymorphism,
this
generates
selection
closer
linkage
(Rice,
1987).
difficult
test
because,
non-recombining
stratum
evolved,
will
present
only
Y-linked
making
analysis
impossible.
Although
mutations
might
detectable
from
expression
sexes
at
(perhaps
higher
males),
degeneration
expected
eventually
old
evolutionary
strata.
Another
approach
population
genomic
evidence
show
associations
alleles
(Dagilis
Qiu
signal
found
partially
it
does
whether
future
lead
recombination.
search
alternatives
explain
ask
ruled
out.
As
described
below,
new
ideas
Testing
predictions
2
below)
requires
studies
newly
evolving
genomes,
becoming
possible,
using
combination
sequencing
mapping.
study
S.
dioica
(closely
related
hybridize
nature
homologous
XY
chromosomes),
published
Journal
Evolutionary
Biology
(Filatov,
2022),
examines
stratum.
Y-
X-linked
nevertheless
ascertained
identifying
male-specific
variants
gene
sequences,
samples
males
natural
populations.
allowed
analyses
mentioned
above
showed
parts
establishment
factor.
Clear
step
those
seen,
numbers
unknown,
species'
genomes
large
human
yet
assembled.
mapping
suggest
extremely
rate
PAR,
thus
differ
mammalian
PARs,
crossover
concentrated
very
(Rouyer
1986).
Some
but
dioica,
suggesting
(and
dioica;
Campos
2016).
end
studied
them
detail.
22
were
both
(they
had
populations),
20
classified
species,
15
appear
forming
young
(much
younger
youngest
ones
humans
above)
suitable
testing
about
suppression.
(MSY)
gradually
expand
hinders
pairing
sequences
meiosis
(Jeffries
2021).
MSY-X
should
increase
distance
into
2).
slight
trend
stratum,
outgroup
vulgaris
increases
so
responsible
(HKA
tests,
correct
effect,
detected
elevated
diversity
suggests
regions).
Interestingly,
sharply
latifolia-specific
shared
change
possibly
discontinuous
1b.
time
makes
seem
unlikely
loss
expansion
across
includes
least
(probably
500
kb,
density
34
genes/Mb).
stickleback
slightly
(Ks),
3%
4%,
Again
Ks
older
predicted.
true
papaya,
2012),
consistent
chromosomal
inversion
models
propose
expansions
involving
chance
inversions
prevent
set
MSY.
advantage
outweigh
fertility
disadvantages
heterozygotes,
production
gametes
duplications
deficiencies
crossovers
occur
paired
inversions.
version
(Jay
Olito
2022)
proposes
prevents
deleterious
homozygous
males.
effect
strongest
highly
recessive
effects.
Accumulation
arises
fixing
population,
must
rapidly
replace
(initially
arrangement).
process
works
best
populations,
account
observations
time-course
formation.
involved,
data
distinguish
previous
one—both
predict
current
boundary.
Only
few
examples
coinciding
boundaries
far
discovered.
inversions,
others
done
(Lemaitre
2009).
cases,
(10
IV
seven
V),
formation
require
genes.
(involving
16
genes)
papaya
2012).
Clearly,
detailed
helpful.
rearrangements,
accumulate
stops
(Charlesworth
1994),
third
model
decrease
expression,
dosage
compensation
simultaneously
alleles'
even
before
major
deterioration
coding
reverting
standard
arrangement
(Lenormand
Roze,
Female-biased
indeed
observed
assumed
decreased
alleles,
while
increased
enough
restore
predicts
bias
quickly
sex-linkage
evolves.
Because
evolves
part
process,
strongly
female-biased
many
older)
sexes.
appears
opposite
way
increasing
reach
level
(in
double
males,
significant
difference
which,
expected,
little
bias).
(reviewed
Bachtrog,
2008).
Genes
compensated
seems
incomplete
It
interesting
already
begun
studied,
well
ones,
percent.
Under
polymorphism
hypothesis
outlined
above,
expect
gene(s)
often
pattern
predicted
just
described),
Overall,
model,
do
fit
observations.
Filatov's
larger
supports
(using
HKA
differences),
variants.
Whether
conclusions
confirmed
once
assembly
becomes
available,
valuable
how
integrated
increasingly
accessible
kinds
allow
empirical
tests
this,
potentially
For
instance,
compared
somatic
tissues,
over-represented
among
biased
155
47
one,
did
relationship
genes'
positions
(Kitano
peer
review
history
article
available
https://publons.com/publon/10.1111/jeb.14137.
commentary
there
no
data.
Proceedings of the Royal Society B Biological Sciences,
Journal Year:
2024,
Volume and Issue:
291(2014)
Published: Jan. 10, 2024
The
maintenance
of
colour
variation
in
wild
populations
has
long
fascinated
evolutionary
biologists,
although
most
studies
have
focused
on
discrete
traits
exhibiting
rather
simple
inheritance
patterns
and
genetic
architectures.
However,
the
study
continuous
their
potentially
oligo-
or
polygenic
bases
remains
rare
populations.
We
studied
genetics
continuously
varying
white-to-rufous
plumage
coloration
European
barn
owl
(
Tyto
alba
)
using
a
genome-wide
association
approach
whole-genome
data
75
individuals.
confirmed
mutation
at
melanocortin-1-receptor
gene
MC1R)
is
involved
identified
two
new
regions,
located
super-scaffolds
9
42.
combination
three
regions
explains
(80.37%,
95%
credible
interval
58.45–100%).
One
discovered
region,
sex
chromosome,
differs
between
extreme
colorations
owls
sharing
specific
MC1R
genotype.
This
region
may
play
role
dimorphism
this
species,
possibly
interaction
with
autosomal
.
thus
provide
insights
into
architecture
variation,
pointing
to
an
oligogenic
basis
potential
epistatic
effects
among
loci
that
should
aid
future
understanding
how
maintained
nature.
Proceedings of the Royal Society B Biological Sciences,
Journal Year:
2024,
Volume and Issue:
291(2024)
Published: June 1, 2024
Evolutionary
conflicts
occur
when
there
is
antagonistic
selection
between
different
individuals
of
the
same
or
species,
life
stages
levels
biological
organization.
Remarkably,
can
within
species
genomes.
In
dynamics
evolutionary
conflicts,
gene
duplications
play
a
major
role
because
they
bring
very
specific
changes
to
genome:
in
protein
dose,
generation
novel
paralogues
with
functions
expression
patterns
evolution
small
antisense
RNAs.
As
we
describe
here,
by
having
those
effects,
duplication
might
spark
conflict
fuel
arms
race
that
takes
place
during
conflicts.
Interestingly,
also
contribute
resolution
within-locus
partitioning
under
an
trade-off.
this
review,
focus
on
intraspecific
including
sexual
and
illustrate
various
roles
compilation
examples.
These
examples
reveal
level
complexity
differences
genomes
ontologies
involved
genomic
location
elements
conflict.
The
provide
blueprint
for
direct
study
these
exploration
presence
similar
other
lineages.
Ecology and Evolution,
Journal Year:
2025,
Volume and Issue:
15(2)
Published: Feb. 1, 2025
ABSTRACT
The
genetic
basis
of
sex
determination
is
typically
conserved
within
species
if
not
broader
lineages.
For
example,
the
stickleback
family
(Gasterosteidae),
AmhY
has
been
identified
as
a
master
sex‐determination
(MSD)
gene
in
multiple
across
two
genera.
By
contrast,
existence
within‐species
variability
frequently
observed
but
provides
an
opportunity
to
understand
evolution
and
turnover
systems.
In
this
study,
we
investigated
consistency
with
which
involved
610
individuals
from
five
brook
(
Culaea
inconstans
)
populations.
We
designed
PCR‐restriction
enzyme
assay
identify
presence
each
individual
recorded
sexual
morphology
field
at
time
capture.
found
that
(presence/absence
did
match
field‐determined
phenotypic
up
44%
population.
This
variation
suggests
mechanism
likely
more
complex
than
thought
when
was
first
implicated
may
still
be
evolving.
Such
further
investigate
how
why
transitions
mechanisms
occur.