Southern Analysis
Procedure (for analysis of genomic DNA
or ordering of clones):
1) Prepare genomic DNA (ref. p. 9.22,
Maniatis) from cultured cells using one T75 flask (wash two times with PBS and
then use a rubber policeman to release), or cells from frozen stock. Wash the cell pellets two times in ice
cold PBS, and depending on size of pellet make up in 300 - 600 µl of TE, pH
8. Add 7.5 volumes of 6 M guanidine HCl/O.1 M NaAcetate (17.2 gm
GuHCl and 1 ml of 3 M NaAcetate made up in 30 ml of ddH2O). Mix on rotator for 1 hr at RT. Prepare a 50 ml conical containing 18
ml of RT 100% ethanol. Using a 5
ml plastic pipet, carefully layer the guanidine HCl dissolved cell pellet below
the ethanol.
2) Using a bunsen burner, prepare a glass
pipet with a looped and sealed end.
Place looped pipet into the ethanol and stir the interface until
completely dispersed. The genomic
DNA collects on the loop. Wash by
transferring to a 10 ml conical containing 5 ml EtOH, and then to another 10 ml
conical with 5 ml of EtOH. Allow
the excess EtOH to drip off (can touch to a Kimwipe to remove but donÕt let it
over dry) and immerse in 1 ml of TE, pH 8 overnight at 4”C. Free the DNA by gently scraping with
fresh sealed pipets. Remove the
pipets and rotate at 4”C (24-48 hrs or longer) until the DNA has
dissolved. Determine DNA
concentration with Hoefer minifluorometer (see Lacrimal Isolation in Lab
Protocols). Note that handling genomic DNA requires: (i) use of tips whose bore
size has been increased by cutting off the end with a sterile scalpel blade,
(ii) for digestions, allow DNA to stand at 4”C for several hours after dilution
and addition of 10 x restriction enzyme buffer), (iii) no vortexing (mix with
sealed end of glass pipet while keeping mixture at 4”C, particularly after
addition of restriction enzyme), and (iv) after digestion for 30 min, add a
second aliquot of restriction enzyme and stir.
3) Digest 10 µg of genomic DNA overnight
with Eco RI, Hind III or Bam HI.
After digestion, concentrate by EtOH precipitation, remove all traces of
EtOH by vacuum, and make up the pellet in gel loading buffer. In control digests, include 10 µg
genomic DNA plus 10-5, 10-6, 10-7 µg of
plasmid containing insert complementary to probe. Load on far side of gel away from test samples. As usual, include size standards. Use a 0.7% agarose mid-size gel in 0.5
x TBE containing EtBr. Run overnight
at 35 V (constant). Similarly for
Southerns for ordering newly identified cDNA clones, restriction cut the
miniplasmid prep with an enzyme which should remove the insert (ie. Eco
RI). Run on gel, as above. If DNA has been stored at 4”C, heat to
56”C before applying to the gel.
4) After electrophoresis, photograph on
transilluminator with florescent ruler.
Cut off the left bottom corner to aid in orientation. Transfer is carried out exactly as in
Northerns. Transfer gel to a clean
glass tray and immediately denatured in 900 ml of 50 mM NaOH/10 mM NaCl (to
893.7 ml of ddH2O add 4.5 ml of 10 N NaOH and 1.8 ml of 5 M NaCl)
for 20 min on a rotator. Carefully
pour off and add 900 ml of 0.1 M Tris, pH 7.6 to neutralize (20 min on
rotator). Pour off and add 900 ml
of 20 x SSC for 45 min with gentle rotation. To keep gel immersed during above steps, can balance an
inverted ddH2O filled 50 ml conical on it, making sure that the top
surface of the gel is wet before placing on the conical.
5) During the above 20 and 45 min steps,
preparations for the overnight transfer can be initiated. Needed are: (i) a glass tray or lucite
box filled to a depth of 2 cm with 10 x SSC, (ii) a lucite support for the gel
(can invert the gel mold in the reservoir), (iii) a long piece of 3 MM paper which stretches over the
lucite gel support on either side into the 10 x SSC; wet with 10 x SSC, (iv)
nitrocellulose (Amersham Hybond ECL) cut to the same size as the gel (wear
gloves in this and all steps), (v) two pieces of 3MM paper cut to the same size
as the gel; place one on the long 3 MM piece and wet with 10 x SSC, (vi) a 6-8 inch stack of paper towels cut to
the same size as the gel, (vii) a glass tray containing ddH2O,
(viii) a glass tray containing 10 x SSC, (ix) two 10Ó x 12Ó pieces of X-ray
film, and (x) flat forceps.
6) To set up the transfer, sandwich the
gel between the X-ray film pieces and carefully invert (do over the 20 x
SSC). Place back side up on the
wetted gel-size 3MM paper (on inverted mold). Remove any air bubbles by gently rolling a capless 50 ml
conical over the gel. Add some 10
X SSC to keep from drying out.
Completely surround the gel with Parafilm or plastic wrap. Next, wet the nitrocellulose paper by
floating on, then immersing in, the ddH2O. Immerse the wet filter in 10 x SSC for 5 min. Holding the filter by two sides,
carefully set down exactly on the gel (canÕt reposition). Carefully roll the capless conical over
the filter to ensure removal of any air bubbles. Add the remaining gel-size piece of 3MM paper (wet with 10 x
SSC) and roll with conical.
Carefully add the cut paper towels to a height of 6Ó. Balance a glass tray on top of the
towels to weigh down; stabilize the tray with tape running down on all sides to
the 10 x SSC reservoir. Cover with
plastic to reduce loss to evaporation.
If transfer is initiated in the morning, carefully change the paper
towels (can reuse the top dry ones) before leaving at the end of the day. Let the transfer go overnight.
7) Have 80”C vacuum oven heating up. Remove the paper towels and, with the
gel/filter still in place, invert.
Use an indelible fine tip marker to mark on the filter the edges of the
gel (including the cut corner) and the loading wells. Record experimental number at the top. Peel off the gel and stain for 45 min
in 0.5 µg/ml ethidium bromide (then place in ddH2O and
examine/photograph on transilluminator).
Place filter in 6 x SSC for 5 min to wash, then place on 3MM paper and
dry for at least 30 min. Place the
dried filter between two pieces of 3MM paper and bake under vacuum for 1-2 hr.
8)
To carry out hybridization to filter,
prehybridize filter for 4 hr at 42”C (in prehyb/hyb. plastic boxes; gently
rotation) in a prewarmed solution of 30% formamide, 5 x SSPE, 0.1% SDS, 5 x
DenhardtÕs, 0.2 mg/ml sonicated denatured salmon sperm DNA.
Prehybridization SolÕn Hybridization
SolÕn
ddH2O 15.3
ml ddH2O 15.3
ml
Formamide 15
ml Formamide 15
ml
20
x SSPE 12.5
ml 20
x SSPE 12.5
ml
20%
SDS 0.25
ml 20%
SDS 0.25
ml
50
x DenhardtÕs 5 ml 50
x DenhardtÕs 5 ml
Salmon
Sp. DNA 2 ml Salmon
Sp. DNA 2 ml
Poly
A 5
µl Poly
A 5
µl
32cDNA
probe 50-100
µl
(note: Salmon Sperm DNA stock is 5 mg/ml; Poly A stock is 10
mg/ml; make up prehyb and hyb solÕns in 50 ml conicals)
9) During prehybridization, label cDNA
probe (purified insert) by random priming method (Pharmacia #27-9251-01). Reconstitute reaction mix by adding 20
µl of ddH2O and place on ice for 5-60 min. Make 1.8 µl of insert up in 25 µl of TE, pH 8 and denature
for 3 min at 95”C. Cool on ice for
2 min, then add diluted/denatured insert to reaction mix. Behind lucite, add 5 µl of 32PdCTP
(ICN #33004X). Carefully mix by
pipetting up and down. Incubate at
37”C for 15-30 min. Purify probe
using a Nick Spin Column (Pharmacia #17-0862-02) or equivalent (Qiagen #28304)
and check cpmÕs in Scintillation counter.
Denature probe (3 min at 95”C, on ice for 2 min) prior to addition to
hybridization solution. Hybridize
overnight at 42”C with gently rotation.
10) Remove filter
into 400 ml of room temperature 2 x SSC, 0.1% SDS (40 ml of 20 x SSC and 4 ml
of 20% SDS made up to 800 ml in ddH2O). Wash for 5 min on rotator. Do two additional washes. Transfer filter to 400 ml of prewarmed (42 - 65”C; use 42”C
for wheat-mouse and 65”C for mouse-mouse hybridizations) 0.1 x SSC, 0.1% SDS (4
ml of 20 x SSC and 4 ml of 20% SDS made up to 800 ml in ddH2O). Wash for 20 min on rotator. Do a total of three 20 min washes.
11) Allow filter
to dry on fresh bench paper, then place on Whatmann 3MM paper in a large x-ray
cassette holder. Cover with
plastic wrap. Under red light in
the dark room, place x-ray film on, followed by an enhancing screen. Close up and expose overnight at -70”C.