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S Sutou

Publications and source records attributed to S Sutou.

At least 37 records · Page 2Linked to original sources

Cloning and sequence analysis of cDNA encoding the bovine testis-derived male-enhanced antigen (Mea).

A full-length cDNA encoding the bovine male enhanced antigen (Mea) has been cloned from a bovine testicular cDNA library and sequenced. The primary structure of the bovine Mea peptide deduced from this nucleotide sequence has 174 amino acid residues and is highly homologous to human (95.9%, 165/172) and mouse (92.5%, 161/174) Mea gene products. It is located on an autosome, and is expressed highly in the testes.

Amino Acid Sequence↗

DNA-damaging, mutagenic, clastogenic and cell-cell communication inhibitory properties of gamma-oryzanol.

As a part of short-term safety assessment of gamma-Oryzanol, the genotoxic or the carcinogenic initiation activity was studied in three genetic toxicity tests and the promotion activity was studied in a cell-cell communication inhibitory test. gamma-Oryzanol showed the negative response in the bacterial DNA repair test (Rec-assay), the bacterial reverse mutation tests (Ames test) and the rat bone marrow chromosome aberration test. Also, gamma-Oryzanol showed the negative response in the metabolic cooperation inhibition test using Chinese hamster V79 cells.

Animals↗

Mutagenicity studies on catena-(S)-[mu-[N alpha-(3-aminopropionyl)histidinato(2-)-N1,N2,O:N tau]-zinc].

Z-103 (catena-(S)-[mu-[N alpha-(3-aminopropionyl)histidinato (2-)-N1,N2,O:N tau]-zinc], CAS 107667-60-7) was examined in the bacterial mutation test, a chromosomal aberration test with mammalian cells in culture and the micronucleus test using male mice. 1. Z-103 did not increase the number of revertants in Escherichia coli WP2 uvrA when tested at up to 5000 micrograms/plate in the presence or absence of metabolic activation. And Z-103 did not increase mutants in Salmonella typhimurium SD 100 (streptomycin dependent strain) or in Salmonella typhimurium TM677 (8-azaguanine sensitive strain) when tested at up to 5000 micrograms/ml in the presence or absence of metabolic activation. 2. The chromosomal aberration test was carried out with cultured Chinese hamster lung cells (CHL). For the direct assay procedure, the cells were treated with 3.3 x 10(-4)-3.3 x 10(-6) mol/l Z-103 for 24 or 48 h, after which time chromosome preparations were made. For the metabolic activation assay procedure, the cells were treated with 1.0 x 10(-3)-3.3 x 10(-6) mol/l of Z-103 for 6 h in the presence or absence of metabolic activation, and the chromosome preparations were made after a further 18-h incubation in the absence of Z-103 and metabolic activation. Z-103 did not cause chromosome aberrations either in the presence or in the absence of metabolic activation. 3. The micronucleus test was performed in ddY male mice. Z-103 was administered orally to mice at a dose of 400, 200 or 100 mg/kg.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Maternal effect on micronucleus induction in MS/Ae mice.

MS/Ae mice, which are mutagen-sensitive in both the dominant lethal test and micronucleus test, and CD-1 mice, which are the parental strain of MS/Ae, were mated in all four possible combinations. Both male and female offspring were subjected to the micronucleus test using mitomycin C (MMC), colchicine (Col), and 6-mercaptopurine (6-MP). Col showed equivocal results. However, MMC and 6-MP showed differential responses in that both male and female offspring from CD-1 dams had lower incidences of micronucleated polychromatic erythrocytes than those from MS/Ae dams regardless of sire strain. In addition, body weights of offspring from MS/Ae dams were lower than those from CD-1 dams regardless of sire strain. Numbers of offspring from MS/Ae dams tended to be smaller than those from CD dams. These results suggest that the traits of MS/Ae mice are associated more with maternal factors than with paternal ones.

Animals↗

Difference between intraperitoneal and oral gavage application in the micronucleus test. The 3rd collaborative study by CSGMT/JEMS.MMS. Collaborative Study Group for the Micronucleus Test/Mammalian Mutagenesis Study Group of the Environmental Mutagen Society of Japan.

In the third collaborative study organized by the Collaborative Study Group for the Micronucleus Test (CSGMT), a task group belonging to the Mammalian Mutagenesis Study subgroup of the Environmental Mutagen Society of Japan (JEMS.MMS), intraperitoneal (i.p.) injection and oral (p.o.) gavage were compared as routes of administration of test chemicals. Two mouse strains, MS/Ae and CD-1, and 17 chemicals with various modes of action were used. The chemicals were 1-beta-D-arabinofuranosylcytosine, 6-mercaptopurine monohydrate, benzo[a]pyrene, 7,12-dimethylbenz[a]anthracene, 2-acetylaminofluorene, phenacetin, cyclophosphamide, ethyl methanesulfonate, N-ethyl-N-nitrosourea, methyl methanesulfonate, mitomycin C, colchicine, vincristine sulfate, potassium bromate, potassium chromate(VI), benzene, and procarbazine hydrochloride. On the basis of the findings of an acute toxicity test and a pilot experiment for dose and sampling time, a full-scale micronucleus test was performed on each chemical. Almost all the chemicals showed a positive response in micronucleus induction by both routes of administration in both mouse strains. Contradictory outcomes were obtained between the i.p. and p.o. routes on potassium chromate in both strains (i.p.: positive, p.o.: negative). In the CD-1 mice, benzene potently induced micronuclei when administered p.o., but gave only a marginal response when administered i.p. Generally, the chemicals induced micronuclei at lower dose levels (mg/kg) when administered i.p. This tendency, however, was decreased or even reversed when the dose was expressed as a percentage of the LD50. Although the i.p. route, an artificial exposure route, is useful to detect the inducibility of micronuclei of a test chemical per se at a small dose, the p.o. route seemed sensitive and valuable enough to evaluate the test chemicals. When the dose levels of chemicals are adjusted on the basis of the LD50, both i.p. injection and p.o. gavage are acceptable as routes of administration in the micronucleus test.

Administration, Oral↗

Administration-route-related differences in the micronucleus test with N-ethyl-N-nitrosourea.

Administration-route-related differences in the micronucleus test were examined by giving N-ethyl-N-nitrosourea (ENU) to male mice of the MS/Ae and CD-1 strains by 2 different routes, intraperitoneally (i.p.) and orally (p.o.). The experiments consisted of 3 parts: (1) a simplified acute toxicity study, which gave LD50s of 490 (i.p.) and 840 mg/kg (p.o.) in MS/Ae and 640 (i.p.) and 960 mg/kg (p.o.) in CD-1 mice: (2) a pilot experiment for the full-scale micronucleus test to determine appropriate dosages and sampling time: and (3) the micronucleus test at doses of 12.5, 25, 50, and 100 mg/kg with a sampling time of 24 h. The results indicated that no route-related differences existed at the 2 lowest doses. At 50 mg/kg, markedly higher numbers of micronucleated polychromatic erythrocytes (MNPCEs) were induced in both mouse strains by the i.p. route. At 100 mg/kg, the difference between the routes decreased in strain CD-1 and even reversed in MS/Ae. Thus, route-related differences appeared to depend on the dose. Such differences became small, however, in both strains when the comparison was made on the basis of LD50 values.

Administration, Oral↗

Base sequence of a cloned snake W-chromosome DNA fragment and identification of a male-specific putative mRNA in the mouse.

A 2.5-kilobase fragment of a sex-specific satellite DNA from the Colubrid snake species Elaphe radiata has been cloned, and its sequence has been determined. It contains 26 and 12 copies, respectively, of two base quadruplets, G-A-T-A and G-A-C-A, as its sole highly repetitious elements. Southern hybridization experiments with genomic DNA of the chicken, the mouse, and man indicated male sex-specific conservation of at least parts of this cloned DNA. In situ hybridization experiments with metaphase chromosomes of the mouse showed that elements that can cross-hybridize with parts of the cloned snake DNA are concentrated in the pericentric region of the Y chromosome. In blot hybridization experiments with liver poly(A)+ polysomal RNAs of male and female mice, a probe consisting of the first 1,224 bases of the cloned snake DNA singled out a male-specific RNA of 1,250-1,400 bases. Inasmuch as the proximal end of this probe contained an open reading frame (44 consecutive amino acid-specifying codons), the male-specific putative mRNA so detected may specify H-Y antigen. By contrast, a probe consisting of bases 1,480-1,906, containing the simple repeats of the quadruplets, singled out a shorter (approximately 1,000-base) RNA from males and females alike. Although this RNA is poly(A)+, we have yet to establish its attachment to ribosomes.

Animals↗

Spontaneous sister-chromatid exchanges in Chinese hamster cells in vivo and in vitro.

The incidence of sister-chromatid exchanges (SCEs) was studied in Chinese hamster cells. The cells used were an established cell line (Don), an aneuploid secondary culture still exhibiting contact inhibition of growth, a primary culture, bone-marrow cells in vivo, a Don-derived clone having ring chromosomes, and endoreduplicated Don cells. The frequency of SCEs in the presence of bromodeoxyuridine (BUdR) increased in the following order: bone-marrow cells less than Don less than secondary culture cells less than primary culture cells. Marked increases in BUdR concentration induced only slight increases of SCEs. Some ring chromosomes showed Moebius strip and concatenated ring structures, indicating spontaneous occurrence of SCEs in the absence of BUdR. The incidence of spontaneous SCEs observed in ring chromosomes approximates that of SCEs observed in ordinary rod chromosomes in the presence of low dose levels of BUdR. SCEs occurring in the first and second cell cycles were separately counted in endoreduplicated cells. The ratio of single SCEs, which occurred in the second cell cycle, to twin SCEs, which occurred in the first cell cycle, was about 2, when the count of single SCEs was corrected for the induction effect. This implies that uninemy chromatids retain the polarity of DNA when SCEs occur, that bifilarly and trifilarly BUdR-substituted DNA strands give equal numbers of SCEs and that incidence of SCEs is independent of the length of S in the Don cells used here.

Animals↗

The mechanisms of endoreduplication.

Chinese hamster cells, Don line, were treated with concanavalin A (ConA), calcium ionophore A23187 (A23187), colchicine, sodium fluoride (NaF), 6-thiopurine, dibutyryl cyclic AMP (db-cAMP), and other nucleotides, alone or in combination. A23187 itself did not induce endoreduplication but did so in combination with ConA. NaF could induce endoreduplication and the combination of NaF and ConA showed a synergistic effect. db-cAMP suppressed the inducing activity of ConA. The findings that various chemicals are inducers of endoreduplication and that synergistic effects appear on combined treatments suggest that various mechanisms of induction of endoreduplication may exist. The chemical nature of the inducers and the suppressor, db-cAMP, implies that blocking of the phosphorylation of some cellular components may be involved as a main mechanism. Analysis of the endoreduplication cell cycle indicated that cells treated with reagents in S require a longer cell cycle than those treated in G2 and that the length of the lag period between induction treatment and the initiation of S, the length of S, and the length of G2 war variable. The inducers, induction mechanisms, and the cell cycle of endoreduplication seem to vary; however, the essence of endoreduplication is the omission of mitotic events by connecting S and G1.

Aneuploidy↗