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Queer Feelings, Political Potential: Tracing Affect in Performance Spaces

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Figure

Figure
1.1.
Schematic
representation
of
HCMV
genome.
The
HCMV
genome
is
divided
into
two
regions
of
sequences,
the
unique
long
(UL)
and
unique
short
(US)
sequence
regions.

The
UL
and
US
are
flanked
by
terminal
repeats:

terminal
repeat
long
(TRL)
and
terminal
repeat
short
(TRS).

The
UL
and
US
are
divided
by
a
series
of
internal
repeats:

internal
repeat
long
(IRL)
and
internal
repeat
short
(IRS).

Adapted
from
(Kotenko
et
al.,
2000).


Figure
1.2.
Human
Cytomegalovirus
replication
cycle.
(A)
Virion
attachment,
entry
and
un‐coating
of
viral
nucleocapsid.

(B)
Transport
of
viral
nucleocapsid
to
the
nucleus
via
microtu‐bules
and
release
of
viral
DNA
and
tegument
proteins
into
nucleus.

(C)
DNA
replication,
tran‐scription,
and
translation
of
viral
proteins
under
cascade
regulation:

IE,
DE,
and
L
genes.

(D)
Capsid
protein
assembly.

(E)
Viral
DNA
encapsidation.


(F)
Nuclear
egress
of
the
viral
nucleo‐capsid.
(G)
Secondary
envelopment
at
endoplasmic
reticulum
golgi
intermediate
compartment
(ERGIC).

(H)
Release
of
viral
progeny.

ER,
endoplasmic
reticulum,
and
GB,
golgi
body.
Based
on
(Knipe
and
Howley,
2007;
Mocarski
Jr,
2007).


Figure
1.3.
Structure
of
the
eye
and
neurosensory
retina.
The
eye
is
divided
into
two
seg‐ments,
the
anterior
and
posterior
segments.

The
anterior
segment
consists
of
the
cornea
and
crystalline
lens,
structures
necessary
for
receiving
and
focusing
light
onto
the
posterior
segment
of
the
eye.

The
posterior
segment
receives
light
at
the
central
point
of
the
retina,
the
fovea,
and
is
then
processed
by
the
cells
of
the
neurosensory
retina
(photoreceptors:

rods
and
cones).

Enlarged
sections
depict
the
cells
and
divisions
of
the
neurosensory
retina.
(Caspi,
2010;
Kolb,
1995d)

Table
1.1.
Mouse
model
of
retrovirus‐induced
immunosuppression
(MAIDS)
development.


+7

References

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