Homologous
centromeres
compete
for
segregation
to
the
secondary
oocyte
nucleus
at
female
meiosis
I.
Centromeric
repeats
also
with
each
other
populate
in
mitotic
cells
of
germline
and
have
become
adapted
use
recombinational
machinery
present
promote
their
own
propagation.
Repeats
are
not
needed
centromeres,
rather
appear
be
hospitable
habitats
colonization
proliferation
repeats.
This
is
probably
an
indirect
consequence
two
distinctive
features
centromeric
DNA.
Centromeres
subject
breakage
by
mechanical
forces
exerted
microtubules
meiotic
crossing-over
suppressed.
proteins
acting
trans
under
selection
mitigate
costs
cis.
Collateral
competition
may
help
explain
high
rates
aneuploidy
observed
early
human
embryos.
Cell,
Год журнала:
2024,
Номер
187(12), С. 3006 - 3023.e26
Опубликована: Май 13, 2024
Centromeres
are
scaffolds
for
the
assembly
of
kinetochores
that
ensure
chromosome
segregation
during
cell
division.
How
vertebrate
centromeres
obtain
a
three-dimensional
structure
to
accomplish
their
primary
function
is
unclear.
Using
super-resolution
imaging,
capture-C,
and
polymer
modeling,
we
show
partitioned
by
condensins
into
two
subdomains
mitosis.
The
bipartite
found
in
human,
mouse,
chicken
cells
therefore
fundamental
feature
centromeres.
Super-resolution
imaging
electron
tomography
reveal
assemble
kinetochores,
with
each
subdomain
binding
distinct
microtubule
bundle.
Cohesin
links
centromere
subdomains,
limiting
separation
response
spindle
forces
avoiding
merotelic
kinetochore-spindle
attachments.
Lagging
chromosomes
cancer
divisions
frequently
have
attachments
which
separated
bioriented.
Our
work
reveals
aspect
biology
implications
understanding
mechanisms
guarantee
faithful
segregation.
Proceedings of the National Academy of Sciences,
Год журнала:
2022,
Номер
120(1)
Опубликована: Дек. 27, 2022
Centromeres
are
the
specialized
regions
of
chromosomes
that
direct
faithful
chromosome
segregation
during
cell
division.
Despite
their
functional
conservation,
centromeres
display
features
rapidly
evolving
DNA
and
wide
evolutionary
diversity
in
size
organization.
Previous
work
found
noncanonical
B-form
structures
abundant
several
eukaryotic
species
with
a
possible
implication
for
centromere
specification.
Thus
far,
systematic
studies
into
organization
function
non-B-form
plants
remain
scarce.
Here,
we
applied
oat
system
to
investigate
role
centromeres.
We
conducted
chromatin
immunoprecipitation
sequencing
using
an
antibody
centromere-specific
histone
H3
variant
(CENH3);
this
accurately
positioned
different
ploidy
levels
identified
series
sequences
including
minisatellites
retrotransposons.
To
define
genetic
characteristics
centromeres,
surveyed
repeat
dyad
symmetries
were
predicted
form
non-B-DNA
vivo.
These
bent
DNA,
slipped
Z-DNA,
G-quadruplexes,
R-loops
prone
within
CENH3-binding
regions.
Dynamic
conformational
changes
occurred
evolution
from
diploid
tetraploid
hexaploid
oat.
Furthermore,
single-molecule
technique
AFM
DNA:RNA
deep
validate
R-loop
enrichment
Centromeric
retrotransposons
exhibited
strong
associations
formation.
Taken
together,
our
study
elucidates
fundamental
character
genome
reveals
its
potential
Abstract
Background
Centromeres
are
essential
for
faithful
chromosome
segregation
during
mitosis
and
meiosis.
However,
the
organization
of
satellite
DNA
chromatin
at
mouse
centromeres
pericentromeres
is
poorly
understood
due
to
challenges
assembling
repetitive
genomic
regions.
Results
Using
recently
available
PacBio
long-read
sequencing
data
from
C57BL/6
strain,
we
find
that
contrary
previous
reports
their
homogeneous
nature,
both
centromeric
minor
satellites
pericentromeric
major
exhibit
a
high
degree
variation
in
sequence
within
between
arrays.
While
most
arrays
continuous,
significant
fraction
interspersed
with
non-satellite
sequences,
including
transposable
elements.
immunoprecipitation
(ChIP-seq),
occupancy
CENP-A
H3K9me3
pericentric
regions,
respectively,
associated
increased
enrichment
homogeneity
these
The
elements
regions
not
part
functional
as
they
lack
enrichment.
Furthermore,
nucleosomes
occupy
spanning
centromeric-pericentric
junctions
low
yet
amount
spreads
locally
centromere
on
telocentric
sides.
Finally,
while
display
well-phased
arrays,
phased.
Interestingly,
class
also
phase
H3K27me3
nucleosomes,
indicating
nucleosome
phasing
an
inherent
property
satellites.
Conclusions
Our
findings
reveal
diversity
sequence,
organization,
structure.
Genome Biology and Evolution,
Год журнала:
2022,
Номер
14(5)
Опубликована: Апрель 19, 2022
Centromeres
are
essential
chromosomal
regions
that
mediate
the
accurate
inheritance
of
genetic
information
during
eukaryotic
cell
division.
Despite
their
conserved
function,
centromeres
do
not
contain
DNA
sequences
and
instead
epigenetically
marked
by
presence
centromere-specific
histone
H3
variant
centromeric
protein
A.
The
functional
contribution
to
centromere
identity
remains
elusive.
Previous
work
found
dyad
symmetries
with
a
propensity
adopt
noncanonical
secondary
structures
enriched
at
several
species.
These
findings
lead
proposal
may
contribute
specification.
Here,
we
analyze
predicted
recently
identified
Drosophila
melanogaster.
Although
only
on
Y
centromere,
find
other
types
structures,
including
melted
G-quadruplexes,
common
features
all
D.
melanogaster
centromeres.
Our
is
consistent
previous
models
suggesting
be
possible
implications
for
Nucleic Acids Research,
Год журнала:
2022,
Номер
50(22), С. 12636 - 12656
Опубликована: Ноя. 16, 2022
The
four
natural
DNA
bases
(A,
T,
G
and
C)
associate
in
base
pairs
(A=T
G≡C),
allowing
the
attached
strands
to
assemble
into
canonical
double
helix
of
(or
duplex-DNA,
also
known
as
B-DNA).
intrinsic
supramolecular
properties
nucleobases
make
other
associations
possible
(such
triplets
or
quartets),
which
thus
translates
a
diversity
structures
beyond
B-DNA.
To
date,
alphabet
is
ripe
with
approximately
20
letters
(from
A-
Z-DNA);
however,
only
few
them
are
being
considered
key
players
cell
biology
and,
by
extension,
valuable
targets
for
chemical
intervention.
In
present
review,
we
summarise
what
about
alternative
(what
they?
When,
where
how
do
they
fold?)
proceed
discuss
further
those
nowadays
therapeutic
targets.
We
more
detail
molecular
tools
(ligands)
that
have
been
recently
developed
target
these
structures,
particularly
three-
four-way
junctions,
order
intervene
biological
processes
involved.
This
new
stimulating
playground
allows
devising
innovative
strategies
fight
against
genetic
diseases.
Molecular Biology of the Cell,
Год журнала:
2025,
Номер
36(4)
Опубликована: Фев. 12, 2025
The
chromatin
of
the
centromere
provides
assembly
site
for
mitotic
kinetochore
that
couples
microtubule
attachment
and
force
production
to
chromosome
movement
in
mitosis.
is
specified
by
nucleosomes
containing
histone
H3
variant,
CENP-A.
constitutive
centromeric-associated
network
(CCAN)
are
assembled
on
CENP-A
enable
separation.
surrounded
pericentromeric
heterochromatin,
which
itself
bound
sequence
specific
binding
protein,
CENP-B.
We
performed
mechanical
experiments
chromosomes
while
tracking
CENP-B
observe
centromere's
stiffness
role
CCAN.
degraded
CENP-C
CENP-N
auxin-inducible
degrons,
we
verified
compromises
CCAN
via
observation
CENP-T
loss.
Chromosome
stretching
revealed
domain
does
not
visibly
stretch,
even
absence
and/or
CENP-N.
Pericentromeric
deforms
upon
application,
∼3-fold
less
than
entire
chromosome.
loss
has
no
impact
pericentromere
stretching.
Chromosome-disconnecting
nuclease
treatments
showed
structural
effects
Our
show
core-centromeric
more
resilient
likely
mechanically
disconnected
from
underlying
chromatin,
pericentric
deformable
yet
stiffer
arms.