bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Jan. 27, 2023
Abstract
Meiotic
recombination
through
chromosomal
crossing-over
is
a
fundamental
feature
of
sex
and
an
important
driver
genomic
diversity.
It
ensures
proper
disjunction,
allows
increased
selection
responses,
prevents
mutation
accumulation;
however,
it
also
mutagenic
can
break
up
favourable
haplotypes.
This
cost/benefit
dynamic
likely
to
vary
depending
on
mechanistic
evolutionary
contexts,
indeed,
rates
show
huge
variation
in
nature.
Identifying
the
genetic
architecture
this
key
understanding
its
causes
consequences.
Here,
we
investigate
individual
rate
wild
house
sparrows
(
Passer
domesticus
).
We
integrate
pedigree
data
identify
autosomal
crossover
counts
(ACC)
intra-chromosomal
allelic
shuffling
r̅
intra
)
13,056
gametes.
Females
had
1.37
times
higher
ACC,
1.55
than
males.
ACC
were
heritable
females
males
(ACC
h
2
=
0.23
0.11;
0.12
0.14),
but
cross-sex
additive
correlations
low
(r
A
0.29
0.32
for
Conditional
bivariate
analyses
showed
that
all
measures
remained
after
accounting
values
opposite
sex,
indicating
sex-specific
evolve
somewhat
independently.
Genome-wide
models
are
polygenic
driven
by
many
small-effect
loci,
which
act
trans
as
global
modifiers.
Our
findings
have
different
potential
birds,
providing
compelling
mechanism
evolution
sexual
dimorphism
recombination.
Annual Review of Genetics,
Journal Year:
2023,
Volume and Issue:
57(1), P. 1 - 63
Published: Oct. 3, 2023
The
raison
d'être
of
meiosis
is
shuffling
genetic
information
via
Mendelian
segregation
and,
within
individual
chromosomes,
by
DNA
crossing-over.
These
outcomes
are
enabled
a
complex
cellular
program
in
which
interactions
between
homologous
chromosomes
play
central
role.
We
first
provide
background
regarding
the
basic
principles
this
program.
then
summarize
current
understanding
events
recombination
and
three
processes
that
involve
whole
chromosomes:
homolog
pairing,
crossover
interference,
chiasma
maturation.
All
these
implemented
direct
physical
interaction
complexes
with
underlying
chromosome
structures.
Finally,
we
present
convergent
lines
evidence
meiotic
may
have
evolved
coupling
to
late-stage
mitotic
morphogenesis.
PLoS Biology,
Journal Year:
2025,
Volume and Issue:
23(1), P. e3002950 - e3002950
Published: Jan. 6, 2025
In
many
eukaryotes,
meiotic
recombination
occurs
preferentially
at
discrete
sites,
called
hotspots.
various
lineages,
hotspots
are
located
in
regions
with
promoter-like
features
and
evolutionarily
stable.
Conversely,
some
mammals,
driven
by
PRDM9
that
targets
away
from
promoters.
Paradoxically,
induces
the
self-destruction
of
its
this
triggers
an
ultra-fast
evolution
mammalian
is
ancestral
to
all
animals,
suggesting
a
critical
importance
for
program,
but
has
been
lost
lineages
surprisingly
little
effect
on
meiosis
success.
However,
it
unclear
whether
function
described
mammals
shared
other
species.
To
investigate
this,
we
analyzed
landscape
several
salmonids,
genome
which
harbors
one
full-length
truncated
paralogs.
We
identified
initiation
sites
Oncorhynchus
mykiss
mapping
DNA
double-strand
breaks
(DSBs).
found
DSBs
clustered
positioned
promoters,
enriched
H3K4me3
H3K36me3
location
depended
genotype
Prdm9
.
observed
high
level
polymorphism
zinc
finger
domain
,
indicating
diversification
positive
selection.
Moreover,
population-scaled
maps
O
kisutch
Salmo
salar
revealed
rapid
turnover
caused
target
motif
erosion.
Our
results
imply
conserved
across
vertebrates
peculiar
evolutionary
runaway
active
hundred
million
years.
PLoS Genetics,
Journal Year:
2022,
Volume and Issue:
18(8), P. e1010141 - e1010141
Published: Aug. 30, 2022
During
meiosis,
crossover
rates
are
not
randomly
distributed
along
the
chromosome
and
their
location
may
have
a
strong
impact
on
functioning
evolution
of
genome.
To
date,
broad
diversity
recombination
landscapes
among
plants
has
rarely
been
investigated
formal
comparative
genomic
approach
is
still
needed
to
characterize
assess
determinants
species
chromosomes.
We
gathered
genetic
maps
genomes
for
57
flowering
plant
species,
corresponding
665
chromosomes,
which
we
estimated
large-scale
landscapes.
found
that
number
per
spans
limited
range
(between
one
five/six)
whatever
genome
size,
there
no
single
relationship
across
between
map
length
size.
Instead,
general
relative
size
chromosomes
rate,
while
absolute
constrains
basal
rate
each
species.
At
level,
identified
two
main
patterns
(with
few
exceptions)
proposed
conceptual
model
explaining
broad-scale
distribution
crossovers
where
both
telomeres
centromeres
play
role.
These
correspond
globally
underlying
gene
distribution,
affects
how
efficiently
genes
shuffled
at
meiosis.
results
raised
new
questions
only
but
also
Proceedings of the National Academy of Sciences,
Journal Year:
2023,
Volume and Issue:
120(14)
Published: March 27, 2023
Plant
breeding
relies
on
crossing-over
to
create
novel
combinations
of
alleles
needed
confer
increased
productivity
and
other
desired
traits
in
new
varieties.
However,
crossover
(CO)
events
are
rare,
as
usually
only
one
or
two
them
occur
per
chromosome
each
generation.
In
addition,
COs
not
distributed
evenly
along
chromosomes.
plants
with
large
genomes,
which
includes
most
crops,
predominantly
formed
close
ends,
there
few
the
swaths
around
centromeres.
This
situation
has
created
interest
engineering
CO
landscape
improve
efficiency.
Methods
have
been
developed
boost
globally
by
altering
expression
anti-recombination
genes
increase
rates
certain
parts
changing
DNA
methylation
patterns.
progress
is
being
made
devise
methods
target
specific
sites.
We
review
these
approaches
examine
using
simulations
whether
they
indeed
capacity
efficiency
programs.
found
that
current
alter
can
produce
enough
benefits
for
programs
be
attractive.
They
genetic
gain
recurrent
selection
significantly
decrease
linkage
drag
donor
loci
schemes
introgress
a
trait
from
unimproved
germplasm
an
elite
line.
genome
sites
were
also
provide
advantage
when
introgressing
segment
harboring
desirable
quantitative
loci.
recommend
avenues
future
research
facilitate
implementation
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2021,
Volume and Issue:
unknown
Published: Aug. 27, 2021
Abstract
Meiotic
recombination
is
highly
regulated
to
ensure
precise
segregation
of
homologous
chromosomes.
Evidence
from
diverse
organisms
indicates
that
the
synaptonemal
complex
(SC),
which
assembles
between
paired
chromosomes,
plays
essential
roles
in
crossover
formation
and
patterning.
Several
additional
“pro-crossover”
proteins
are
also
required
for
intermediates
become
crossovers.
These
typically
form
multiple
foci
or
nodules
along
SCs,
later
accumulate
at
fewer,
widely
spaced
sites.
Here
we
report
C.
elegans
CDK-2
stabilize
all
stabilizes
interactions
among
pro-crossover
factors
by
phosphorylating
MSH-5.
Additionally,
show
conserved
RING
domain
ZHP-3/4
diffuse
SC
remain
dynamic
following
their
accumulation
Based
on
these
previous
findings
propose
a
model
arise
through
spatially
restricted
biomolecular
condensation
then
undergo
coarsening
process,
resulting
interference.
Genetics,
Journal Year:
2023,
Volume and Issue:
225(2)
Published: Aug. 24, 2023
Abstract
Meiosis
is
a
specialized
cell
division
program
that
essential
for
sexual
reproduction.
The
two
meiotic
divisions
reduce
chromosome
number
by
half,
typically
generating
haploid
genomes
are
packaged
into
gametes.
To
achieve
this
ploidy
reduction,
meiosis
relies
on
highly
unusual
chromosomal
processes
including
the
pairing
of
homologous
chromosomes,
assembly
synaptonemal
complex,
programmed
formation
DNA
breaks
followed
their
processing
crossovers,
and
segregation
chromosomes
during
first
division.
These
embedded
in
carefully
orchestrated
differentiation
with
multiple
interdependencies
between
metabolism,
morphogenesis,
waves
gene
expression
together
ensure
correct
delivered
to
next
generation.
Studies
budding
yeast
Saccharomyces
cerevisiae
have
established
essentially
all
fundamental
paradigms
meiosis-specific
metabolism
uncovered
components
molecular
mechanisms
underlie
these
conserved
processes.
Here,
we
provide
an
overview
stages
key
model
system
highlight
how
basic
genome
stability,
architecture,
cycle
control
been
adapted
unique
outcome
meiosis.
Nature Ecology & Evolution,
Journal Year:
2024,
Volume and Issue:
8(7), P. 1337 - 1352
Published: June 5, 2024
Despite
deep
evolutionary
conservation,
recombination
rates
vary
greatly
across
the
genome
and
among
individuals,
sexes
populations.
Yet
impact
of
this
variation
on
adaptively
diverging
populations
is
not
well
understood.
Here
we
characterized
fine-scale
landscapes
in
an
divergent
pair
marine
freshwater
threespine
stickleback
from
River
Tyne,
Scotland.
Through
whole-genome
sequencing
large
nuclear
families,
identified
genomic
locations
almost
50,000
crossovers
built
maps
for
marine,
hybrid
individuals
at
a
resolution
3.8
kb.
We
used
these
to
quantify
factors
driving
rates.
found
strong
heterochiasmy
between
but
also
differences
ecotypes.
Hybrids
showed
evidence
significant
suppression
overall
map
length
individual
loci.
Recombination
were
lower
only
within
marine-freshwater-adaptive
loci,
loci
same
chromosome,
suggesting
selection
linked
gene
'cassettes'.
temporal
sampling
along
natural
zone,
that
recombinants
traits
associated
with
reduced
fitness.
Our
results
support
predictions
divergence
cis-acting
modifiers,
whose
functions
are
disrupted
hybrids,
may
play
important
role
maintaining
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: March 7, 2024
Abstract
In
many
eukaryotes,
meiotic
recombination
occurs
preferentially
at
discrete
sites,
called
hotspots.
various
lineages,
hotspots
are
located
in
regions
with
promoter-like
features
and
evolutionarily
stable.
Conversely,
some
mammals,
driven
by
PRDM9
that
targets
away
from
promoters.
Paradoxically,
induces
the
self-destruction
of
its
this
triggers
an
ultra-fast
evolution
mammalian
is
ancestral
to
all
animals,
suggesting
a
critical
importance
for
program,
but
has
been
lost
lineages
surprisingly
little
effect
on
meiosis
success.
However,
it
unclear
whether
function
described
mammals
shared
other
species.
To
investigate
this,
we
analyzed
landscape
several
salmonids,
genome
which
harbors
one
full-length
truncated
paralogs.
We
identified
initiation
sites
Oncorhynchus
mykiss
mapping
DNA
double-strand
breaks
(DSBs).
found
DSBs
clustered
positioned
promoters,
enriched
H3K4me3
H3K4me36
marks
location
depended
genotype
Prdm9
.
observed
high
level
polymorphism
zinc
finger
domain
,
not
Moreover,
population-scaled
maps
O.
kisutch
Salmo
salar
revealed
rapid
turnover
caused
target
motif
erosion.
Our
results
imply
conserved
across
vertebrates
peculiar
evolutionary
runaway
active
hundred
million
years.