bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 15, 2024
Summary
The
tight
regulation
of
meiotic
recombination
between
homologs
is
disrupted
in
Brassica
AAC
allotriploids,
a
genomic
configuration
that
may
have
facilitated
the
formation
rapeseed
(
napus
L.)
∼7,500
years
ago.
Indeed,
presence
haploid
C
genome
induces
supernumerary
crossovers
homologous
A
chromosomes
with
dramatically
reshaped
distribution.
However,
genetic
mechanisms
driving
this
phenomenon
and
their
divergence
nascent
established
lineages
remain
unclear.
To
address
these
concerns,
we
generated
hybrids
carrying
additional
derived
either
from
an
lineage
allotetraploid
B.
or
its
diploid
progenitor
oleracea
.
We
then
assessed
variation
across
twelve
populations
by
mapping
male
using
Single
Nucleotide
Polymorphism
markers
evenly
distributed
sequenced
genome.
Our
findings
reveal
C09
chromosome
responsible
for
near
pericentromeric
regions.
Interestingly,
counterpart
shows
no
significant
effect
on
own,
despite
having
similar
content
genes.
showed
influences
crossover
through
inter-chromosomal
epistatic
interactions
other
specific
chromosomes.
These
results
provide
new
insights
into
emphasize
role
since
allopolyploid
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 8, 2025
Abstract
During
meiosis,
the
correct
pairing,
synapsis,
and
recombination
of
homologous
chromosome
pairs
is
critical
for
fertility
sexual
eukaryotes.
These
processes
are
challenged
in
polyploids,
which
possess
additional
copies
each
chromosome.
Polyploidy
thus
provides
a
unique
context
to
study
how
evolution
can
modify
meiotic
programs
response
challenges.
We
previously
observed
that
Arabidopsis
arenosa
newly
formed
(neo-)polyploids,
synapsis
defects
precede
chromosomes
associating
aberrant
multivalent
univalent
configurations.
Here
we
dynamics
genotypes
with
varying
levels
stability
ask
whether
efficient
synaptic
progression
key
component
evolving
stable
tetraploid
meiosis.
develop
method
quantify
using
foci
pro-crossover
factor
HEI10
as
reference.
initially
appears
at
many
small
loci
before
accumulating
only
crossover
sites.
In
diploids,
this
transition
begins
while
there
still
significant
asynapsis,
quickly
declines
accumulation
fewer
progresses.
neo-tetraploids,
suboptimal
elongation
initiation
sites,
perhaps
defective
precedes
stalling
onset
accumulation.
established
tetraploids,
when
asynapsis
minimal,
suggesting
an
enhanced
HEI10/synapsis
co-dynamic
(even
compared
diploids).
Hybrids
generated
by
crossing
neo-
tetraploids
exhibit
intermediate
phenotypes.
find
extent
correlates
positively
numbers,
well
higher
frequency
multivalents
univalent,
disturb
segregation.
Our
work
supports
hypothesis
improving
efficiency
important
polyploid
stability.
Significance
Statement
pair
subsequently
form
synaptonemal
complex,
maturation
DNA
events.
How
formation
coordinated
where
multiple
sets
complicate
pair-wise
interactions,
remains
unclear.
Leveraging
‘developmental
clock,’
quantified
new
.
Synapsis
severely
compromised
ones
it
more
even
than
diploids.
Notably,
correlated
excess
crossovers,
compromises
connecting
connect
homologs
multivalents.
findings
highlight
polyploids.
Meiotic
crossover
recombination
is
essential
for
both
accurate
chromosome
segregation
and
the
generation
of
new
haplotypes
natural
selection
to
act
upon.
This
requirement
known
as
assurance
one
example
control.
While
conserved
role
ATPase,
PCH-2,
during
meiotic
prophase
has
been
enigmatic,
a
universal
phenotype
when
pch-2
or
its
orthologs
are
mutated
change
in
number
distribution
crossovers.
Here,
we
show
that
PCH-2
controls
crossovers
by
antagonizing
their
formation.
antagonism
produces
different
effects
at
stages
prophase:
early
prophase,
prevents
double
strand
breaks
from
becoming
crossover-eligible
intermediates,
limiting
formation
sites
initial
break
homolog
interactions.
Later
winnows
contributing
designation
ultimately,
assurance.
We
also
demonstrate
accomplishes
this
regulation
through
HORMAD,
HIM-3.
Our
data
strongly
support
model
which
PCH-2’s
remodel
HORMADs
throughout
destabilize
precursors,
coordinate
with
synapsis,
contribute
progressive
implementation
recombination,
guaranteeing
BMC Genomics,
Journal Year:
2025,
Volume and Issue:
26(1)
Published: Feb. 10, 2025
The
accumulation
of
cadmium
(Cd)
in
ryegrass
(Lolium
multiflorum
Lamk.)
as
a
widely
used
pasture
plant
poses
serious
risk
to
food
safety.
This
study
aimed
investigate
the
differences
phenotypes,
physiology,
and
expression
metal
transporters
between
four
genotypes
(diploid/tetraploid
Cd-tolerant/sensitive).
diploid/Cd-sensitive
were
found
uptake,
accumulate,
translocate
more
Cd
compared
tetraploid/Cd-tolerant
genotypes.
with
soluble
components
facilitated
transfer
from
root
shoot
sensitive
Tetraploid
Cd-tolerant
Chuansi
No.1
accumulated
less
shoots
but
higher
ratio
cell
wall,
making
it
promising
model
for
studying
mechanisms
resistance
stress.
complex
regulatory
system
dilution
effect
contributed
lower
uptake
tetraploid
Moreover,
exhibited
genes
that
promoted
efflux,
which
could
contribute
their
accumulation.
Overall,
this
sheds
light
on
physiological
transcriptional
by
different
polyploids,
providing
guidance
breeding
soil
improvement.
New Phytologist,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 18, 2025
Summary
Polyploidy
plays
a
key
role
in
genome
evolution
and
crop
improvement.
The
formation
of
bivalents
rather
than
multivalents
during
meiosis
polyploids
is
essential
to
ensure
meiotic
stability
optimal
fertility
the
species.
However,
mechanisms
preventing
multivalent
recombination
remain
obscure.
We
studied
synaptonemal
complex
polyploid
by
mutating
transverse
filament
component
ZYP1
allotetraploid
Brassica
napus
autotetraploid
Arabidopsis.
In
B.
,
mutation
all
four
copies
results
pairing
accompanied
partner
switches,
nonhomologous
recombination,
interlocks,
leading
severe
chromosome
entanglement
abortion.
presence
only
one
functional
allele
compromises
synapsis
associations
occur
at
nonsynaptic
regions.
Moreover,
disruption
causes
complete
shift
from
predominantly
exclusively
pachytene
cells
synthetic
Arabidopsis
thaliana
resulting
dramatic
increase
frequency
metaphase
I.
conclude
that
ZYP1‐mediated
assembly
facilitates
pairwise
homologous
both
allopolyploid
autopolyploid
species
ensuring
diploid‐like
bivalent
meiosis.
Meiotic
crossover
recombination
is
essential
for
both
accurate
chromosome
segregation
and
the
generation
of
new
haplotypes
natural
selection
to
act
upon.
This
requirement
known
as
assurance
one
example
control.
While
conserved
role
ATPase,
PCH-2,
during
meiotic
prophase
has
been
enigmatic,
a
universal
phenotype
when
pch-2
or
its
orthologs
are
mutated
change
in
number
distribution
crossovers.
Here,
we
show
that
PCH-2
controls
crossovers
by
antagonizing
their
formation.
antagonism
produces
different
effects
at
stages
prophase:
early
prophase,
prevents
double-strand
breaks
from
becoming
crossover-eligible
intermediates,
limiting
formation
sites
initial
break
homolog
interactions.
Later
winnows
contributing
designation
ultimately,
assurance.
We
also
demonstrate
accomplishes
this
regulation
through
HORMAD,
HIM-3.
Our
data
strongly
support
model
which
PCH-2’s
remodel
HORMADs
throughout
destabilize
precursors
coordinate
with
synapsis,
ensuring
progressive
implementation
explaining
function
pachytene
checkpoint
Journal of Integrative Plant Biology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 21, 2025
Seedlessness
is
a
most
valuable
trait
in
fruit
crops
for
fresh
consumption
and
processing.
The
mutations
essential
meiosis
genes
are
known
to
confer
sterility
seed
abortion
plants.
However,
defects
have
rarely
been
reported
crops.
Here,
we
found
caused
seedless
citrus
bud
sport
cultivar,
with
massive
unpaired
univalents
during
diakinesis,
indicating
disruption
crossover
formation.
A
non-functional
CrMER3A-103
bp
allele
103-bp
deletion
the
gene
body,
together
other
CrMER3a
T
exon,
were
identified
cultivar.
CrMER3
protein
was
undetectable
at
meiotic
prophase
I
knock
out
of
resulted
precocious
Mini-citrus.
Therefore,
natural
variation
responsible
seedlessness
this
originated
from
primitive
wild
mandarin
passed
cultivated
mandarins.
Kompetitive
Allele-Specific
PCR
(KASP)
marker
developed
identify
germplasm
screen
potential
sterile
hybrids
cross
breeding.
Uncovering
enhances
our
understanding
mechanisms
controlling
facilitates
breeding
varieties.
Proceedings of the National Academy of Sciences,
Journal Year:
2025,
Volume and Issue:
122(19)
Published: May 7, 2025
During
meiosis,
the
correct
pairing,
synapsis,
and
recombination
of
homologous
chromosome
pairs
is
critical
for
fertility
sexual
eukaryotes.
These
processes
are
challenged
in
polyploids,
which
possess
additional
copies
each
chromosome.
Polyploidy
thus
provides
a
unique
context
to
study
how
evolution
can
modify
meiotic
programs
response
challenges.
We
previously
observed
that
newly
formed
(neo-)polyploids
Arabidopsis
arenosa
,
synapsis
defects
precede
chromosomes
associating
aberrant
multivalent
univalent
configurations.
Here,
we
dynamics
genotypes
with
varying
levels
stability
ask
whether
efficient
synaptic
progression
key
component
evolving
stable
tetraploid
meiosis.
develop
method
quantify
using
foci
pro-crossover
factor
HEI10
as
reference.
initially
appears
at
many
small
before
accumulating
only
crossover
sites.
In
diploids,
this
transition
begins
while
significant
asynapsis
still
present,
though
it
quickly
declines
accumulates
fewer
foci.
neo-tetraploids,
suboptimal
elongation
initiation
sites
stalled
perhaps
due
defective
occurs
onset
accumulation.
established
tetraploids,
accumulation
when
near
complete,
suggesting
enhanced
HEI10/synapsis
codynamics
(even
compared
diploids).
Hybrids
generated
by
crossing
neo-
tetraploids
exhibit
intermediate
phenotypes.
find
extent
correlates
positively
numbers,
frequency
multivalents
univalents,
disturb
segregation.
Our
work
supports
hypothesis
improving
efficiency
important
polyploid
stability.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 13, 2024
Abstract
Meiotic
crossover
recombination
is
essential
for
both
accurate
chromosome
segregation
and
the
generation
of
new
haplotypes
natural
selection
to
act
upon.
While
conserved
role
ATPase,
PCH-2,
during
meiotic
prophase
has
been
enigmatic,
a
universal
phenotype
that
observed
when
pch-2
or
its
orthologs
are
mutated
change
in
number
distribution
crossovers.
Here,
we
show
PCH-2
controls
crossovers
by
antagonizing
formation.
This
antagonism
produces
different
effects
at
stages
prophase:
early
prophase,
prevents
double
strand
breaks
from
becoming
crossovers,
limiting
sites
initial
DSB
formation
homolog
interactions.
Later
winnows
crossover-eligible
intermediates,
contributing
reinforcement
designation
ultimately,
assurance.
We
also
demonstrate
accomplishes
this
regulation
through
HORMAD,
HIM-3.
Our
data
strongly
support
model
which
PCH-2’s
remodel
HORMADs
throughout
destabilize
precursors,
coordinate
with
synapsis,
contribute
progressive
implementation
recombination,
guaranteeing
control.
Meiotic
crossover
recombination
is
essential
for
both
accurate
chromosome
segregation
and
the
generation
of
new
haplotypes
natural
selection
to
act
upon.
While
conserved
role
ATPase,
PCH-2,
during
meiotic
prophase
has
been
enigmatic,
a
universal
phenotype
that
observed
when
pch-2
or
its
orthologs
are
mutated
change
in
number
distribution
crossovers.
Here,
we
show
PCH-2
controls
crossovers
by
antagonizing
formation.
This
antagonism
produces
different
effects
at
stages
prophase:
early
prophase,
prevents
double
strand
breaks
from
becoming
crossovers,
limiting
sites
initial
DSB
formation
homolog
interactions.
Later
winnows
crossover-eligible
intermediates,
contributing
reinforcement
designation
ultimately,
assurance.
We
also
demonstrate
accomplishes
this
regulation
through
HORMAD,
HIM-3.
Our
data
strongly
support
model
which
PCH-2’s
remodel
HORMADs
throughout
destabilize
precursors,
coordinate
with
synapsis,
contribute
progressive
implementation
recombination,
guaranteeing
control.