Interphase chromosomes were isolated in good yield from four species of fungi. In no case does the chromatin contain histones such as are characteristic of the chromosomes of other eukaryotic organisms

Dill, B. C.

Leighton, T. J.

Phillips, Cornell

Stock, J. J.

Caltech Authors - Main

Proceedings of the National Academy of Sciences
Vol. 68, No. 3, pp. 677-680, March 1971
Absence of Histones from the Chromosomal Proteins of Fungi
T. J. LEIGHTON*, B. C. DILL, J. J. STOCK, AND CORNELL PHILLIPSt
Department of Microbiology, University of British Columbia, Vancouver, B.C., Canada, and
t Division of Biology, California Institute of Technology, Pasadena, Calif. 91109
Communicated by James Bonner, January 11, 1971
ABSTRACT Interphase chromosomes were isolated in
good yield from four species of fungi. In no case does the
chromatin contain histones such as are characteristic of
the chromosomes of other eukaryotic organisms.
That histones are characteristic chromosomal proteins has
been demonstrated for a wide variety of eukaryotic creatures.
Thus, the chromosomes of higher plants and animals not only
contain histones but, in addition, these proteins are similar in
number, chemical properties, and even, in some cases, in
primary structure (1, 2). Histones chemically similar to those
of higher plants and animals have been found in the green alga
Chlorella (3) and in the protozoan Tetrahymena (4, 5), as
well as in a wide variety of invertebrates.
There have been several reports that the nuclei and/or
chromatin of fungi lack histones, but contain instead chromo-
somal proteins of a less basic nature (6-9). We have examined
the basic chromosomal proteins of several fungi, using what
we believe to be the most rigorous of techniques for both
chromatin isolation and histone characterization.
We describe methods for obtaining purified fungal chroma-
tin that result in the recovery of at least 70% of the DNA
present in the homogenate. The possibility of proteolytic deg-
radation of histones (if present) is unlikely. We find that
histones analogous to those cf higher eukaryotes are missing in
the fungi we have examined.
MATERIALS AND METHODS
Chromatin isolation
Attempts to isolate chromatin from the fungus M4icrosporum
gypseum by the methods suggested for liver and pea (10) were
not successful. Fungal nuclei are sheared by these methods,
and centrifugal forces sufficient to pellet the chromatin result
in gross RNA contamination of the nuclear fraction. A more
viscous grinding medium should afford greater protection to
the nuclei during the cell breakage step. Stern's glycerol
grinding medium admirably satisfied this requirement (11).
Sporulation and spore purification procedures for Micro-
sporum have been described previously (12, 13). 2-liter Erlen-
meyer flasks, containing 600 ml of glucose (1% w/v) and neo-
peptone (Difco, 1% w/v) (pH 6.5), were inoculated with 106
conidia per ml and shaken at 350 rpm on a New Brunswick
controlled environment dry-air shaker (30"C) for 4 days.
The mycelia were harvested by suction filtration. The myce-
lial mat (150 g wet weight) was washed 4 times with 1-liter
amounts of ice-cold physiological saline (pH 6.5).
The mycelial mat was resuspended in 350 ml of grinding
medium (glycerol 50% w/v, 0.5 M sucrose, 0.001 M CaCl2,
and 0.05M Tris, pH 8). The slurry was poured into an alumi-
num container and frozen by the addition of liquid nitrogen.
Several additions of liquid nitrogen were necessary to com-
pletely freeze the material. The frozen slurry was ground to a
coarse powder and placed into a Waring blendor. When the
temperature of the grinding solution reached -30'C, the
blendor was turned to full speed (110 V). Homogenization
was continued until the temperature reached 0C. The homog-
enate was again poured into an aluminum container and
partially frozen (to -20'C) by the addition of liquid nitrogen.
The partially frozen slurry subsequently was homogenized at
full speed until the temperature reached 0C. The freezing
and homogenization steps were repeated until 70% breakage
was observed under a microsope (usually 3-4 cycles). The
homogenate was filtered two times through 1 layer of Mira-
cloth and then two times through 3 layers of Miracloth.
The filtrate was centrifuged at 10,000 X g for 10 min. The
supernatant fraction was then removed with a large-bore
pipette and centrifuged at 30,000 X g (Sorvall SS-1, 16,000
rpm) for 1 hr. The pellet (90% DNA recovery) was resus-
pended in 90 ml of grinding solution. The resuspended
nuclei were centrifuged again at 10,000 X g for 10 min and the
supernatant fraction was removed. The 10,000 X g superna-
tant fluid was centrifuged then at 30,000 X g for 1 hr. The
pellet (90% DNA recovery) was resuspended in 10 ml of 0.01
M Tris, pH 8, and stirred slowly overnight at 0C. The nu-
clear lysate was centrifuged at 30,000 rpm (Spinco, 30 rotor)
for 20 min. The supernatant fraction was removed and layered
onto a discontinuous gradient, consisting of 1 ml of 50% su-
crose (in 0.01 M Tris, pH 8) overlaid by 0.5 ml of 20% sucrose
(in 0.01 M Tris, pH 8). The chromatin was recovered by
centrifugation for 14 hr at 35,000 rpm (Spinco SW-39 rotor).
The pellet (80% DNA recovery) was resuspended in 0.01 M
Tris, pH 8, and dialyzed (4 hr) against 200 volumes of 0.01 M
Tris, pH 8. Aggregated material was removed by centrifuga-
tion at full speed in a clinical centrifuge (approx. 3,000 X g)
for 30 sec. The clear supernatant fluid (70% DNA recovery)
was used for all subsequent experiments. This material ex-
hibits the typical ultraviolet absorption spectrum reported for
isolated chromatins (10) (Fig. 1). Approximately 200 ,ug of
DNA (as chromatin) was recovered from 150 g (wet weight)
of mycelia.
Chromatin was prepared from mycelia of Neurospora tetra-
sperma, just as described above. In the case of Neurospora
crassa, chromatin was precipitated from French-press homog-
* Present address: Department of Biochemistry and Biophysics,
University of California, Davis, Calif.
677
678 Biochemistry: Leighton et al.
2 2
z
4
0.1
230 260 280 300
WAVELENGTH (nm)
FIG. 1. Ultraviolet absorption spectra of M. gypseum chro-
matin and DNA. - - -, chromatin; , DNA. DNA was obtained
by pelleting chromatin through 4 M CsCl (35,000 rpm for 24 hr,
Spinco 39 rotor) as described by Bonner et al. (10).
enates of mycelia by 0.15 M NaCl and the resulting material
was purified by centrifugation through 1.8 M sucrose. In the
case of Phycomyces blakesleeanus, nuclei were readily prepared
from squeezed extracts of sporangiophores (stage IV). Chro-
matin was purified from the lysed nuclei by centrifugation
through 1.8M sucrose.
RESULTS
Table 1 summarizes the chemical composition of M. gypseum
chromatin and its nuclear fractions. The low ratio of total
chromosomal protein to DNA results from a low ratio of basic
proteins to DNA in the chromosomal and nuclear fractions.
The amounts of nonbasic chromosomal protein and of RNA
are similar to those reported for other eukaryotic cells (10).
It is our experience that RNA to DNA ratios of greater than
0.05:1 should raise a suspicion of ribosomal contamination.
This may explain why we find very low amounts of basic
protein in our chromosomal fraction while others have re-
ported larger amounts of "slightly basic" proteins in fungal
chromatin (8).
The low ratio of basic protein to DNA suggests either that
histone-like proteins are not a major component of chromo-
somal proteins in this organism or that they are degraded
during the isolation procedure. To assess the possibility of
TABLE 1. Chemical composition of M. gypseum chromatin
and nuclear fractions*
Total Basic
Source protein DNA RNA protein
Nuclear
fraction 15. 17 (+0. 05) 1 2.00(±0.02) 0.05(±0.0a)
Chromatin 1.05 (40 . 05) 1 0.05 (+0. 02) 0.03 (+0. 05)
* Protein was estimated by the Folin reaction (16) and DNA
by the diphenylamine method (17). RNA was measured by the
orcinol reaction (10). Nuclear-fraction values are the average of
four experiments. Chromatin values are the average of six ex-
periments. Basic protein was extracted with 0.4 N H2SO4, 0.2 N
HCl, or with 1 M CaCl2 (10, 17). All of these procedures gave
equivalent values.
degradation, trout testis nucleohistone (gift of K. Marushige)
was added to the nuclear fraction and this material was car-
ried through the subsequent isolation steps. The histone to
DNA ratio of fish nucleohistone was identical before and
after recovery from the M. gypseum chromatin fraction. Disc
gel electrophoresis profiles of the recovered histones were
identical to those reported for this material by Marushige and
Dixon (14). Attempts to demonstrate proteolytic activity
(as measured by incubation of M. gypseum nuclear homoge-
nates with fish histones at 370C for 1 hr at pH 8 or 5) were
negative. It appears unlikely that histones are proteolytically
degraded during isolation of chromatin from Ml. gypseum.
Figs. 2 and 3 show disc electropherograms of the basic and
acidic protein fractions of M. gypseum chromatin. Gel elec-
trophoresis of the small amount of extractable basic protein
(either from chromatin or nuclei) did not demonstrate any
bands that migrated in the histone area. Sodium dodecyl
sulfate-gel separation of the nonhistone chromosomal pro-
teins indicated the presence of 6 major bands and 5 minor
bands (apparent as small peaks or shoulders on the scan).
This profile is reproducible and suggests the limited hetero-
geneity of fungal acidic chromosomal proteins (as detectable
by our separation methods), as is the case with the chromatin
of other eukaryotes (15).
Fig. 4 shows the template activity for RNA synthesis of
M. gypseum chromatin in the presence of added Escherichia
coli RNA polymerase. M. gypseum chromatin possesses 40-
50% of the template activity of deproteinized DNA. The
chromatin used caused no detectable hydrolysis of tritiated
mouse RNA (a gift of Dr. J. Hudson) and did not, therefore,
contain any considerable amount of RNase that might have
decreased or prevented template activity. The high template
activity of fungal chromatin is perhaps t3 be expected, since
A
FIG. 2. Gel electrophoretic separation of M. gypseum chro-
mosomal proteins. The origin is at the top in all photographs. (A)
Fish histone (20 jog separated on polyacrylamide-urea gels ac-
cording to Bonner et al. (10). (B) M. gypseum acid-soluble proteins
(10 ,ug) separated on polyacrylamide-urea gels according to
Bonner et al. (10). (C) M. gypseum nonhistone chromosomal
proteins separated on sodium dodecyl sulfate-polyacrylamide-
urea gels (18, 19). The method is a modification of that of Elgin
and Bonner (15).
Proc. Nat. Acad. Sci. USA 68 (1971)
B
Fungal Chromatin Lacks Histones 679
z
at9
0
4a F
DIRECTION OF MIGRATION 4 DIRECTION OF MIGRATION
FIG. 3. Densitometric tracings of M. gypseum chromosomal proteins (see Fig. 2). The origin is on the left in all figures. Gels were
scanned with a Gilford linear transporter (Model 2410) fitted to a Model 2400 recording spectrophotometer. 6-cm gels were scanned at 2
cm per minute (560 nm). A 0.1 X 2.36-cm aperture plate was employed to maintain band resolution.
histones are apparently absent from it. Van der Vliet et al.
(6) have reported that yeast chromatin also exhibits high
template activity for RNA synthesis. These results suggest
It)
O DNA
0
E
1-S _
X05t<~~~~~roChrmatn
2 4 8 16
jig DNA as Chromatin or DNA/025mi
FIG. 4. RNA synthesis directed by M. gypseum chromatin and
DNA, as a function of template concentration. Template activity
was determined as described by Marushige and Dixon (14). DNA
was prepared as in Fig. 1 (10). 114 jug of E. coli RNA polymerase
was present per 0.25-ml reaction mixture. Incorporation by the
enzyme alone has been subtracted.
that a larger portion of the fungal genome is available for
transcription than is the case in higher eukaryotic cells.
The chromatin of Neurospora tetrasperma was studied by
methods identical to those outlined above. This chromatin, as
well as that prepared from lysed Phycomyces nuclei, was puri-
fied by sucrose density gradient centrifugation and extracted
with acid as outlined above. Such extracts also failed to yield
detectable histone as judged by disc-electrophoretic mobility.
The chromatin of Neurospora crassa, prepared as described
above, was extracted with 0.4 N H2SO4, and the resulting
(very sparse in amount) acid-soluble proteins were prepared
for disc electrophoresis as described by Bonner et al. (10).
Such electrophoresis revealed no proteins with mobilities
characteristic of histones.
DISCUSSION
We have found histones to be absent from the chromatins of
Microsporum gypseum (fungi imperfecti), Neurospora tetra-
sperma and N. crassa (ascomycetes), and Phycomyces blake-
sleeanus (phycomycete). Dwivedi et al. (8) have found his-
tones to be absent from the chromatin of Neurospora crassa;
we confirm their result. Histones appear to be absent from the
chromatins of ascomycetes and lower fungi; we have not yet
investigated any basidiomycete.
Histones of similar amino acid composition, end groups,
electrophoretic mobilities, and primary structure are found in
higher plants and animals, as well as in invertebrates, the
green alga Chlorella, and the protozoan Tetrahymena. The
Proc. Nat. Acad Sci. USA 68 (1971)
680 Biochemistry: Leighton et al.
fungi that we have investigated seem to differ from other
eukaryotes in that they lack these characteristic chromosomal
proteins, which suggests that the fungi may have branched
at an early level from the main stream of eukaryote evolution.
We are indebted to Profs. James Bonner, Max Delbruck, and
Keiji Marushige for their helpful discussions and advice. We
thank Louise Avent for excellent technical assistance and Dr.
Ruth Dusenbery and Stanley Froehner for their help in certain
phases of this work.
This work was supported in part by a grant provided by the
Medical Research Council, Ottawa, Canada, and in part by U.S.
Public Health Service Grant GM 13762.
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Absence of histones from the chromosomal proteins of fungi

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Absence of histones from the chromosomal proteins of fungi

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