3.5 Fluorescence In
Situ Hybridization
(FISH) in Fixed Cells
with the RT-Aptamer
[25]
- Fix HeLa cells on 96-well plates (3.0 103 cells per well) with
a 4% paraformaldehyde at room temperature for 15 min. - Wash the cells twice with PBS.
- Permeabilize the cells with 70% ethanol overnight at 4C.
- Soak the cells in 2SSC buffer at 50C for 15 min.
- Incubate the cells at 37C for 24 h with the prehybridization
buffer. - Incubate the cells with 100 ng of the RT-aptamer in 2SSC
buffer (50μL) for 2 h at 37C. - Treat the cells with 30μLof1μg/mL Hoechst 33342 in
2 SSC buffer at 37C for 30 min. - Add a 30μLof5μM BHQ1-Cy3 probe in 2SSC buffer,
incubate at 37C for 30 min, and then wash out excess probe
with 2SSC buffer. - Observe the target RNAs under a confocal microscope (see
Note 16).
3.6 Preparation of an
Expression Vector
Encoding RT-Aptamer
[26–28]
- Prepare the dsDNA template encoding RT-aptamer by anneal-
ing two 100μM synthetic ssDNA oligos, RT aptamer tem-
plates 1 and 2 [Fig.3] in annealing buffer. - Prepare the ligation mixture usingBglII–HindIII linearized
pSuper.neo plasmid as a vector, and incubate the mixture for
30 min at 16C to allow the ligation reaction. - Transform DH5αwith the ligation product, and heat shock at
42 C for 1 min and spread the cells on an LB plate containing
100 μg/mL of carbenicillin.
GG GCU
G
G
G
CC
C
U
U
UU
A
A
A
A
A
A
U
A
U
U
A
U
G
C
C
GA
C
A
U
A
G
G
A
G
RNA Targeting Arm
Removal of
stem region
Addition of
RT arm
Recognition of
target RNA
U U
5’
3’
5 ’ 3 ’
AAUGAAGAUCAAGAUCAUUGCUCC
Target RNA
5’3’
C
U
A
C
G
A
G
G
U
A U
G
C
AAA
U
A
GC
AU
GC
U
U
U
G
CG
CG
CG
GG
G
U
.
.
5’ 3’
AUGCAGGA AG
C
UA
C
G
A
G
G
U
A
U
G
C
AAA
U
UU U
CG
G
UAUACUUCUG
AAUGAAGAUCA UAC UUGCUCC
AGA
3’. 5’
GG GCU
G
G
G
CC
C
U
U
UU
A
A
AA
A
A
U
Fig. 2Preparation of the BHQ1-binding RNA aptamer
314 Shin-ichi Sato et al.