Hydrobiological Journal,
Journal Year:
2023,
Volume and Issue:
60(1), P. 54 - 68
Published: Dec. 8, 2023
Using
four
microsatellite
DNA
markers
(<i>Mch
5,
Mch
8,
MT
203,
282</i>),
the
genetic
diversity
and
population
structure
of
three
groups
mussels
from
north-western
section
Black
Sea
were
analyzed,
Baltic
North
Seas
studied
as
outgroups.
By
(MS)
loci,
59
alleles
determined
in
five
mussels'
(<i>n</i>
=
118).
The
observed
heterozygosity
(<i>H<sub>O</sub></i>)
ranged
0.083
to
0.538
was
lower
than
expected
(<i>H<sub>E</sub></i>
0.344-0.858).
All
mussel
showed
heterozygote
deficiency,
which
suggests
possibility
inbreeding.
Weak
(<i>F<sub>ST</sub></i>
0.036-0.048)
moderate
0.054-0.127)
differentiation
between
revealed.
Genetic
distances
different
locations
calculated,
0.211
1.130.
obtained
data
confirmed
by
cluster
coordinate
analyzes
carried
out
using
distribution
frequencies.
ABSTRACT
Detecting
external
chemosensory
cues
via
Class-A
G
protein-coupled
receptors
(GPCRs)
is
essential
for
behavioral
and
biological
functions,
influencing
animal
evolution
ecological
adaptations.
While
well-studied
in
vertebrates
echinoderms,
their
role
major
clades
like
Lophotrochozoa
less
understood
despite
remarkable
Utilizing
238
lophotrochozoan
genomes
across
eight
phyla,
we
conducted
a
large-scale
comparative
genomics
analysis
to
identify
lineage-specifically
expanded
subsets
(LSEs)
of
GPCRs
adapted
chemoreception.
Using
phylogeny
orthology-based
clustering,
differentiated
these
expansions
from
conserved
orthogroups
endogenous
ligand-binding
GPCRs.
LSEs
correlated
with
adaptations
diverse
habitats,
whole-genome
duplications
having
limited
impact.
Across
species
coastal,
freshwater,
terrestrial
habitats
exhibited
large
LSEs,
while
those
extreme
deep-sea
environments,
parasitic
lifestyles,
or
alternative
mechanisms
showed
consistent
reductions.
Sequence
heterogeneity,
positive
selection,
pocket
flexibility
further
underscored
environmental
signals.
These
findings
provide
foundational
insights
into
GPCR-mediated
chemoreception
Lophotrochozoa.
Teaser
Unveiling
correlations
between
lophotrochozoans
habitat
lineage-specific
changes
GPCR
repertoire.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2022,
Volume and Issue:
unknown
Published: Nov. 18, 2022
Abstract
The
blue
mussel,
Mytilus
edulis
is
part
of
the
species
complex,
encompassing
at
least
three
putative
species:
M.
edulis,
galloprovincialis
and
trossulus
.
These
occur
on
both
sides
Atlantic
hybridize
in
nature,
are
important
aquaculture
species.
They
also
invasive
many
parts
world.
Here,
we
present
a
chromosome-level
assembly
We
used
combination
PacBio
sequencing
Dovetail’s
Omni-C
technology
to
generate
an
with
14
long
scaffolds
containing
94%
predicted
length
genome
(1.6
out
1.7
Gb).
Assembly
statistics
were
total
1.65
Gb,
N50
=
116
Mb,
L50
7
and,
L90
13.
BUSCO
analysis
showed
92.55%
eukaryote
BUSCOs
identified.
AB-
Initio
annotation
using
RNA-seq
from
mantle,
gills,
muscle
foot
47,128
genes.
gene
models
combined
Isoseq
validation
resulting
65,505
129,708
isoforms.
Using
GBS
shotgun
sequencing,
sequenced
3
North
American
populations
characterize
single-nucleotide
as
well
structural
variance.
This
high-quality
for
provides
platform
develop
tools
that
can
be
breeding,
molecular
ecology
evolution
address
questions
commercial
environmental
perspectives.
Hydrobiological Journal,
Journal Year:
2023,
Volume and Issue:
60(1), P. 54 - 68
Published: Dec. 8, 2023
Using
four
microsatellite
DNA
markers
(<i>Mch
5,
Mch
8,
MT
203,
282</i>),
the
genetic
diversity
and
population
structure
of
three
groups
mussels
from
north-western
section
Black
Sea
were
analyzed,
Baltic
North
Seas
studied
as
outgroups.
By
(MS)
loci,
59
alleles
determined
in
five
mussels'
(<i>n</i>
=
118).
The
observed
heterozygosity
(<i>H<sub>O</sub></i>)
ranged
0.083
to
0.538
was
lower
than
expected
(<i>H<sub>E</sub></i>
0.344-0.858).
All
mussel
showed
heterozygote
deficiency,
which
suggests
possibility
inbreeding.
Weak
(<i>F<sub>ST</sub></i>
0.036-0.048)
moderate
0.054-0.127)
differentiation
between
revealed.
Genetic
distances
different
locations
calculated,
0.211
1.130.
obtained
data
confirmed
by
cluster
coordinate
analyzes
carried
out
using
distribution
frequencies.