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Enhancer RNAs (eRNAs) are a class of non-coding RNA transcripts that originate from enhancer regions in the genome. They are typically produced by RNA polymerase II at active enhancers and are often transcribed in a bidirectional fashion from loci marked by enhancer-associated chromatin signatures such as H3K4me1 and H3K27ac. eRNAs are usually short, unstable transcripts that are not routinely polyadenylated, and they tend to have short half-lives compared with messenger RNAs. Their expression is highly tissue- and stimulus-specific and generally correlates with the activity of the nearby enhancer and the transcriptional output of their target genes.

The functional significance of eRNAs remains a topic of research and debate. In some contexts, the presence

eRNAs are typically detected using methods that capture transcription or nascent RNA, such as global run-on

of
eRNA
transcription
correlates
with
higher
enhancer
activity
and
with
elevated
expression
of
nearby
genes;
perturbations
that
reduce
eRNA
production
can
sometimes
decrease
target
gene
expression
or
affect
enhancer-promoter
looping.
However,
other
studies
suggest
that
eRNA
transcription
can
be
a
byproduct
of
an
active
enhancer
rather
than
a
required
mechanism,
and
not
all
enhancers
producing
transcripts
show
a
measurable
regulatory
effect
on
gene
expression.
sequencing
(GRO-seq)
and
precision
run-on
sequencing
(PRO-seq),
or
RNA
sequencing
approaches
that
enrich
for
nascent
transcripts.
They
are
generally
shorter
than
2
kilobases
and
are
rapidly
degraded,
contributing
to
challenges
in
detection
by
standard
RNA-seq.
eRNA
biology
is
an
active
field,
with
ongoing
work
to
determine
the
extent
to
which
individual
eRNAs
contribute
causally
to
gene
regulation.