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M C Yoshida

Publications and source records attributed to M C Yoshida.

At least 145 records · Page 8Linked to original sources
PubMed1986

Assignment of the gene for human DNA polymerase beta (POLB) to chromosome 8.

A cloned cDNA segment of 442 bp which contains the region coding the N-terminal sequence of rat DNA polymerase beta polypeptide was used as a probe in Southern hybridization analysis to identify the gene for this enzyme. This probe hybridized with DNA from mouse and human in addition to rat DNA, and the BamHI fragment containing DNA polymerase beta gene sequence was unique in size in each species: 15.8 kb for rat DNA, 8.7 kb for mouse DNA and 10.1 kb for human DNA. DNA extracted from a panel of 12 independent human-mouse somatic cell hybrids was analyzed by Southern blot hybridization with the cloned cDNA probe. The results indicate that the gene for the human DNA polymerase beta sequence (POLB) is located on chromosome 8.

Animals↗
PubMed1986

[The gene map].

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Animals↗
PubMed1985

Genes for insulin I and II, parathyroid hormone, and calcitonin are on rat chromosome 1.

Insulin, parathyroid hormone, and calcitonin are polypeptide hormones that regulate important physiological processes in target tissues. Rat genes encoding each hormone were chromosomally assigned to rat chromosome 1. Both rats and mice have two insulin genes (I and II). However, in contrast to mice in which insulin I and II are asyntenic, rat insulin I and II were both localized to chromosome 1. This study identifies a conserved syntenic group on rat chromosome 1, and implies that mouse insulin I and II genes were chromosomally separated after rats and mice diverged 20-35 million years ago.

Animals↗
PubMed1985

Absence of extensive recombination between inter- and intraspecies mitochondrial DNA in mammalian cells.

Recombination of mammalian mitochondrial DNA (mtDNA) was examined using mouse X rat somatic cell hybrid clones and rat cybrid clones. The mouse X rat hybrids were isolated by fusion of chloramphenicol-sensitive (CAPs) mouse and CAP-resistant (CAPr) rat cells. The rat cybrids were isolated by fusion of rat cells with type B mtDNA and enucleated cells with type A mtDNA. Genetic and physical analyses showed that the mtDNAs of the hybrids and cybrids were simple mixtures of the two parental mtDNAs except in the following two cases: One was subclone H2-9 of mouse X rat hybrids, which was CAPr even though mtDNA from the CAPs mouse parent was predominantly retained. The other was rat cybrid subclones, Y12-24 and -61, which showed specific loss of one Hinf I fragment of type B mtDNA, B10. These observations suggest that, in contrast to the case with plant mtDNA, recombination of mammalian mtDNA occurs rarely, if at all.

Animals↗
PubMed1985

Pleiotropic phenotypic expression in cybrids derived from mouse teratocarcinoma cells fused with rat myoblast cytoplasts.

Cybrid clones were isolated by fusing mouse embryonal carcinoma (PCC4) cells with cytoplasts of rat myoblastic cells (L6TG X CAPr). Although some clones were similar to PCC4 (Type II), a high proportion (88%) were differentiated; the differentiated cells had a mesh-like arrangement (Type I) or were flat with many projections (Type III). Protein patterns of both Type I and Type III cells changed markedly from that of PCC4 cells. Type III cells lacked alkaline phosphatase and expressed endo A and B proteins predominantly. One Type III clone produced alpha-fetoprotein and plasminogen activator (visceral endoderm-like), while another clone consisted of trophectodermal cell-like giant cells. Therefore it was shown that introduction of the somatic cell cytoplasm induces differentiation of teratocarcinoma stem cells, suggesting a cytoplasmic element (or elements) regulating gene expression.

Alkaline Phosphatase↗
PubMed1985

Gene mapping in the Chinese hamster and conservation of syntenic groups and Q-band homologies between Chinese hamster and mouse chromosomes.

Using Chinese hamster/mouse somatic cell hybrids segregating hamster chromosomes, we assigned 15 enzyme genes to six different Chinese hamster autosomes. Of the 15 loci, three genes, HK1, PEPC, and SORD, were newly assigned to chromosomes 1, 5, and 6, respectively, while ENO1, PGD, and PGM1 were assigned to the long arm of chromosome 2, in the segment 2q113----qter. The locations of the following loci were confirmed: ESD, NP, and PEPB on chromosome 1, ME1 and MPI on chromosome 4, AK1 on chromosome 6, and GPI and PEPD on chromosome 9. Comparative mapping of Chinese hamster and laboratory mouse chromosomes revealed conservation of syntenic groups and extensive banding homology between the Chinese hamster and mouse chromosomes on which homologous enzyme markers have been mapped.

Animals↗
PubMed1985

Establishment and characterization of Ph1-positive and Ph1-negative lymphoblastoid cell lines from a patient with chronic myelogenous leukemia.

Two continuously growing in vito cell lines, PB-1049 and LN-1049, were established from a patient with Ph1-positive chronic myelogenous leukemia in extramedullary blastic crisis. PB-1049 was established from Epstein-Barr virus (EBV)-infected peripheral lymphocytes of the patient and had a 46,XY,t(9;22) karyotype. This cell line was shown to be tumorigenic in nude mice, and cultured cells recovered from the tumor nodule showed a 46,XY,6p+,t(9;22) stem line karyotype. LN-1049 was derived from a lymph node culture of the same patient, and was found to be non-tumorigenic in nude mice and karyotypically normal. Immunological examinations on EBV-induced antigens, surface and cytoplasmic immunoglobulin, and monoclonal antibodies, and some enzymatic and electron microscopic studies revealed that both cell lines had attained differentiation into late-B cell stage.

Animals↗
PubMed1985

Regional mapping of the human proto-oncogene c-yes-1 to chromosome 18 at band q21.3.

Human proto-oncogene c-yes-1 homologous to the viral oncogene (v-yes) of an avian Y73 sarcoma virus was mapped to region q21.3 of chromosome 18 by in situ hybridization. This finding confirmed and more rigidly substantiated the previous assignment which was based on analyses of human X mouse somatic cell hybrids and Southern blots.

Chromosome Mapping↗
PubMed1984

Isolation and characterization of intraspecific cybrids. Effect of mitochondrial DNA on their cellular properties.

Cybrid clones were obtained by fusing whole cells of rat glioma C6BU-1, resistant to 5-bromodeoxyuridine (BrdU), with cytoplasts of embryonic rat 3Y1CAP cells, resistant to chloramphenicol (CAP), in selective medium with BrdU and CAP. The clones resistant to BrdU and CAP were confirmed to be cybrids by chromosome and mtDNA analyses. More than half the mtDNA of all the cybrid clones was from the 3Y1CAP cells. After cultivation of a cybrid clone Y22 for 3 months in the absence of CAP, subclones were isolated. One subclone Y22-22 contained predominantly mitochondrial DNA (mtDNA) from the 3Y1CAP cells. Using this subclone, the effects of the mitochondrial genome on cellular properties were examined. The growth patterns, expression of glioma-specific beta-adrenergic receptor, and composition of the major proteins of C6BU-1 cells were not affected by transmitted mtDNA from the 3Y1CAP cells. This procedure for isolating cells containing predominantly foreign mtDNA will be useful in studies on the interaction between genomes of the mitochondria and nucleus.

Animals↗
PubMed1984

Correction of sister chromatid exchanges in Bloom's syndrome fibroblasts after fusion with cytoplasts from a Chinese hamster cell line.

Cytoplasmic hybrids (cybrids) were prepared by fusion of Bloom's syndrome (BS) fibroblasts with cytoplasts derived from a chloramphenicol (CAP)-resistant cell line of hypoxanthine phosphoribosyl transferase (HPRT)-deficient Chinese hamster wg3h cells to study the role of cytoplasmic and nuclear factors which may involve corrective factor(s) of sister chromatid exchanges (SCEs) of the BS cells. The high rate of SCEs characteristic of the cultured BS fibroblasts was found to be fully corrected in cybrids. This result suggests the existence of a transmissible corrective factor(s) in the cytoplasm of the Chinese hamster cells. Long-term cultures of such cybrids after 3 and 5 weeks of fusion, however, showed a reversion to a high SCE level similar to the parental BS cells, indicating that the corrective factors have not been stable in the cybrid cells.

Animals↗
PubMed1984

Chromosomal assignment of the gene for human elongation factor 2.

Elongation factor 2 (EF-2), polypeptidyl -tRNA translocase, is an essential factor for protein synthesis in eukaryotic cells and Archebacteria . We isolated diphtheria toxin-resistant human primary embryo cells that contain EF-2 that cannot be ADP-ribosylated by diphtheria toxin and Pseudomonas exotoxin A (PA toxin). Somatic cell hybrids were constructed from mouse L cells and toxin-resistant human embryo cell mutants. Forty-one hybrid clones were isolated, of which 15 clones were resistant to PA toxin. Karyotypic analysis and isozyme studies revealed that there was an absolute correlation between human chromosome 19 and resistance to PA toxin in the hybrids. On subcloning of PA toxin-resistant hybrid cells, we obtained one PA toxin-resistant hybrid subclone containing human chromosome 19 as the only human chromosome. Furthermore, the resistance to PA toxin of hybrid cell strains was lost after infection with poliovirus, for which sensitivity is conferred by human chromosome 19. It was confirmed by using two-dimensional gel electrophoresis that PA toxin resistance in hybrid cells was caused by the presence of EF-2 resistant to ADP-ribosylation by fragment A of diphtheria toxin. These facts suggest that the gene encoding EF-2 is located on human chromosome 19.

ADP Ribose Transferases↗
PubMed1984

Effect of mitochondrial DNA transmitted cytoplasmically from nontumorigenic to tumorigenic rat cells on the phenotypic expression of tumorigenicity.

The effect of mitochondrial DNA (mtDNA) on the phenotypic expression of tumorigenicity was examined by its cytoplasmic transmission from nontumorigenic cells to tumorigenic cells. Enucleated cells of the rat embryonic cell line 3Y1CAP, which are nontumorigenic and resistant to chloramphenicol, were fused with whole cells of the rat glioma C6BU-1 line, which are tumorigenic and resistant to 5-bromodeoxyuridine, and the cybrid colonies growing in selective medium with 5-bromodeoxyuridine (30 micrograms/ml) and chloramphenicol (50 micrograms/ml) were isolated clonally. Cytoplasmic transmission of 3Y1CAP mtDNA to C6BU-1 cells was confirmed by quantitative analysis of their mtDNA with restriction endonuclease. Subclones containing various amounts of mtDNA from 3Y1CAP cells were isolated from one cybrid clone, Y22, and their tumorigenicities were examined by inoculating 2 X 10(6) cells s.c. into nude mice. The tumorigenicities of these cybrid cubclones were almost identical to that of the nuclear donor C6BU-1 cells with respect to the tumor incidence (number of animals bearing tumors per number of animals inoculated), latent period, and growth rates of tumors. Moreover, analysis of chromosomes and mtDNAs of the cells recovered from the tumors obtained showed that the tumors were derived from the cells inoculated and that no selective overgrowth of segregants that had lost mtDNA from 3Y1CAP cells occurred in the nude mice. These observations suggest that expression of tumorigenicity of C6BU-1 cells was not suppressed by cytoplasmic transmission of nontumorigenic 3Y1CAP mtDNA.

Animals↗
PubMed1983

Two distinct types of mitochondrial DNA segregation in mouse-rat hybrid cells. Stochastic segregation and chromosome-dependent segregation.

Two distinct patterns of mitochondrial DNA (mtDNA) segregation were found in different mouse-rat hybrid cell lines. On mouse-rat hybrid cell line, H2, retained complete sets of chromosomes and mtDNAs of both mouse and rat. Even after cultivation for about one year after cloning, the H2 cell population still retained both parental mtDNAs. However, when mtDNAs of H2 subclones were examined, it was found that some individual cells in the H2 cell population contained only mouse or only rat mtDNA, although they still retained complete sets of both kinds of parental chromosomes. This type of mtDNA segregation, named stochastic segregation, is bidirectional and may be caused by the repetition of random sharing of mouse and rat mtDNAs with daughter cells. This segregation occurred spontaneously during long-term cultivation. The second type of mtDNA segregation, named chromosome-dependent segregation, was found in the other mouse-rat hybrid cell lines that segregated either mouse or rat chromosomes. In these hybrid cells, chromosomes and mtDNA of the same species co-segregated. This second type of segregation is unidirectional. The types of mtDNA segregation appear to depend on the stability of the parental chromosomes in the hybrid cells. When both mouse and rat chromosomes retain stably, mtDNA shows stochastic segregation. On the contrary, when either species of chromosomes is segregated from the cells, mtDNA shows chromosome-dependent segregation.

Animals↗
PubMed1983

Protein synthesis and tumorigenicity of the cytoplasmic hybrid between rat yolk sac tumor and mouse fibroblastic cell line.

Cytoplasmic hybrid (cybrid) cell lines were formed by fusing whole cells of rat yolk sac tumor cell line (EST-II) with cytoplasts of mouse fibroblastic cell line (B-82cap), a variant of mouse L cell line that is deficient in thymidine kinase (TK-) and resistant to chloramphenicol (capr). The cybrid cell line with the nucleus of EST-II and cytoplasma of B-82cap was successfully obtained using double selection with HAT and chloramphenicol-containing medium. The cybrid's ability to synthesize proteins such as albumin, alpha-fetoprotein, gamma-EST, and gamma-GTP was found to be approximately one-fourth that of the nuclear donor, EST-II, at a early time of growth in culture, but this was followed by a gradual increase during the period of observation. The nude mice undergoing subcutaneous transplantation of 1 X 10(6) cells of EST-II and cybrid were killed by the tumor growth, with the survival time being 56 +/- 11 and 105 +/- 25 days, respectively. The histologic findings of cybrid tumor closely resembled those of the nuclear donor, EST-II. These facts suggest that factors from both the nucleus and cytoplasma will be able to affect the gene expression of the cybrid cell line.

Animals↗
PubMed1983

C-band patterns of chromosomes in 17 strains of mice.

Differences in the size and distribution of chromosomal C-bands were investigated in 17 strains of Mus musculus. Each strain was found to have a characteristic C-band pattern. Closely related strains, substrains, and congenic strains, e.g., DDD and DRC, BALB/c and BALB/cAn, and CBA/J and CBA/H-T6, showed a similar C-band pattern, whereas striking dissimilarities in the C-band pattern was observed between the related strains, DDD and DHS, and SJL and SWJ, which were established independently from noninbred stocks of dd and Swiss mice, respectively. Virtually every autosome except for 1 and 2 showed C-band variation among the strains. The size of the C-band on 1, 2, and the X appeared to be fairly constant among the strains. All chromosome pairs were homomorphic in each inbred animal; the between-strain difference in the C-band size was most easily observed in F1 hybrids which showed the heteromorphic C-band patterns, expected from the parents. Measurements of the chromosome lengths of the heteromorphic pairs in a (C57BL/6J X DDD) F1 hybrid disclosed that homologues which had different size C-band had significantly different lengths, and homologues, one of which lacked C-band material, were the same length. Heteromorphism in the length of Y chromosome was also found; BALB/cAn had a Y smaller than the 19. These chromosome markers appear to be useful for characterizing each strain as well as for monitoring inbred stocks.

Animals↗
PubMed1982

Mitochondrial DNA analysis of mouse-rat hybrid cells: effect of chloramphenicol selection on the relative amounts of parental mitochondrial DNAs.

Several mouse-rat somatic hybrid cell lines were isolated by fusing chloramphenicol-resistant (CAPr) and CAP-sensitive (CAPs) parent cells, and propagation of the parent mitochondrial DNA (mtDNA) species in the hybrid cells was studied. The restriction endonucleases EcoRI, HpaII, and HaeIII were used for identification of mtDNA species. Both mouse and rat mtDNAs were propagated in all the hybrid cells examined and maintained during long-term cultivation and repeated cell division. Moreover, in CAPr mouse-rat hybrid cells, selection and successive cultivation in the presence of CAP did not increase the relative amount of mtDNA species of CAPr parent cell origin, and when CAP was removed from the culture medium, mtDNA species of CAPr parent cell origin did not decrease appreciably. The amount of mouse mtDNAs was consistently 1-4 times that of rat mtDNAs inthe mouse-rat hybrid cells regardless of the species of parent cells from which the CAP resistance was derived. Thus mouse-rat hybrid cells have a stable mtDNA population in which the amount of mouse mtDNAs is larger than that of rat mtDNAs without any influence of CAP selection.

Animals↗