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Results for “polyploidization”

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At least 415 records · Page 23Linked to original sources
PubMed1982

[Formation of aberrant polyploid hepatocytes in exposure to the alkylating preparation dipin and to stimulation of proliferation].

One month after the treatment of mice with the alkylating drug Dipin followed by partial hepatectomy 4.7--35.1% of hepatocytes with micronuclei and nuclear bridges in liver were registered. The ploidy level sharply increased. Aberrant cells were the most polyploid ones (16c, 32c). The DNA-fuchsin content in these aberrant polypolid cells decreased by 10--15% due to degrading and non-replication of DNA in the micronuclei.

Alkylating Agents↗
PubMedDate not supplied

[Effect of carbon and nitrogen sources on pullulan biosynthesis by polyploid strains of Pullularia pullulans].

The effect of eight carbohydrates and three nitrogen sources on the activity of pullulan accumulation was studied with a haploid strain, a diploid strain and a tetraploid strain of Pullularia pullulans. The rate of pullulan biosynthesis was found to be the highest in media containing glucose, sucrose and maltose. In this case, the activity of the polysaccharide synthesis in the polyploid strains exceeded that in the haploid strain by 21-80% depending on the carbon source in the medium. The pullulan synthesizing activity of the tetraploid strain depended on the nature of these carbohydrates to a lesser extent than in the case of the haploid and diploid strains. The activity of pullulan synthesis was influenced noticeably by the source of nitrogen in the medium. The greatest amounts of pullulan were accumulated by the three strains in a medium with sodium nitrate.

Carbon↗
PubMed1980

Polyploidization of extraembryonic tissues during mouse embryogenesis.

It has recently been shown that visceral yolk-sac endoderm is derived from the primitive endoderm of the 4.5-day mouse blastocyst (Gardner & Papaioannou, 1975; Gardner & Rossant, 1979). During development, primitive endodermal cells acquire nuclei with more than four times the haploid amount of DNA. The finding of metaphases with multiple sets of chromosomes suggests that the diploid precursors of such endodermal giant cells become truly polyploid. Amniotic cells also contain giant nuclei but the mechanism by which these arise is uncertain. The giant-cell transformation therefore appears to be a general feature of mouse extraembryonic development rather than a phenomenon restricted solely to trophoblast. The basis and significance of these findings are discussed in relation to the development of other extraembryonic membranes both of plant and animal origin.

Animals↗
PubMed1981

Some flow cytofluorimetric studies of the nuclear ploidy of mouse hepatocytes. II. Early changes in nuclear ploidy of mouse hepatocytes following carbon tetrachloride administration: evidence for polyploid nuclei arrested in telophase.

Mature mice have a large proportion of their hepatocyte nuclei in polyploid states (tetraploid and octaploid), and this is more prominent in females. We measured nuclear ploidy distribution cytometrically using ethidium bromide-stained hepatocyte nuclei liberated by in situ collagenase perfusion of the liver via the portal vein. After s.c. administration of 0.2 ml carbon tetrachloride the ploidy distributions of 8-month-old female mice changed from a control of 35% 2N, 45% 4N, and 20% 8N to 54% 2N, 45% 4N and 1% 8N at 6 h, and 65% 2N, 35% 4N and 0% 8N at 24 h. By 72 h 92% of the nuclei were diploid. These changes preceded any changes in mitotic index and S-phase index (3H-TdR autoradiographs). Histology confirmed the loss of higher-ploid nuclei but without mitotic figures or selective cell necrosis to account for the observations. Cleaved nuclei were prominent in sections of liver examined 3 h after CCl4 administration and suggested division of polypoid nuclei that had undergone prior segregation of chromatids and had presumably been arrested in telophase.

Animals↗
PubMedDate not supplied

[Comparison of inactivated rabies vaccines obtained from diploid and polyploid heterologous cells (Hak, BHK, and Vero)].

Homologous or heterologous diploid or polyploid cells have been established as good producers of virus. In this study we present three types of experimental inactivated antirabies vaccines obtained under identical conditions from three types of cells. The study concerns the following characteristics of the vaccines: protecting powers, rabies antigens and major polypeptidic components; this study was performed on supernatants of tissue cultures and concentrated and purified vaccines. Moreover, some cellular and serum contaminants as well as minor rabies proteins were analysed in the viral solutions. It, thus, appears that all these types of vaccines have a similar protecting power (Number of 50% protective doses/micrograms viral protein).

Animals↗
PubMed1980

[Fragmentation of polyploid nuclei in rat trophoblast giant cells. II. Formation of deep folds in the nuclear envelope--the beginning of fragmentation].

Using light and electron microscopy, the nuclear envelope (NE) of the trophoblast giant cells has been examined at the beginning of the spontaneous fragmentation of nuclei on the last days of pregnancy (not long before their degeneration). In the course of the polyploid nucleus division, deep and narrow invaginations appear in the NE, frequently running through the whole nucleus, from one pole towards the other, and separating it into fragments. Short finger-like outgrowings are seen extending from the long invaginations perperdicularly or at a certain angel. Both the nuclear membrances, having numerous nuclear pores, are involved in the formation of these invaginations and shorter extentions. Local enlargements are seen produced in the perinuclear space, mainly in the area of NE invaginations. Narrow folds, separating the giant nucleus into fragments, are filled with the cytoplasm rich in ribosomes. In the nuclear fragments so produced, association between the earlier dispersed chromatin and the NE becomes stronger. Large accumulations of the condensed chromatin are mainly distributed under the NE, only a few minute chromatin blocks being found in the center of the nucleus filled up with diffuse chromatin.

Animals↗
PubMed1994

Mode of inheritance of the higher degree of megakaryocyte polyploidization in C3H mice. I. Evidence for a role of genomic imprinting in megakaryocyte polyploidy determination.

C3H mice have higher average ploidy megakaryocytes than all other mouse strains tested, but the mode of inheritance of this anomaly is unknown. Therefore, to clarify the genetics of high ploidy megakaryocytes in C3H mice, we measured megakaryocyte DNA content from both male and female offspring from F1, as well as backcross matings. In all, offspring from seven different matings of mice were studied: (1) C57BL X C57BL (the first strain listed is the male parent in each case), (2) B6C3F1 (offspring from C57BL X C3H mating) X C57BL, (3) C57BL X B6C3F1, (4) C57BL X C3H, (5) C3H X B6C3F1, (6) B6C3F1 X C3H, and (7) C3H X C3H. The polyploid megakaryocyte DNA content distributions of the offspring from these matings show that C3H mice have higher percentages of high ploidy megakaryocytes than did all other mice. Also, male mice had significantly higher percentages of high ploidy (32N and 64N) megakaryocytes than did female mice for all matings, except backcross mating no. 6. The megakaryocyte DNA content for individual offspring of a given backcross appeared to form a single, continuous distribution, rather than segregate into two distinct groups, suggesting that the higher megakaryocyte DNA content of C3H mice is caused by involvement of multiple allelles. This conclusion is further supported by our finding that the frequency of high ploidy megakaryocytes among offspring of the various matings was related to the proportion of C3H genotype contributed by the parents, ie, average megakaryocyte DNA content increased linearly (r2 = .88 for male mice and .84 for female mice. P < .0001) with increasing C3H gene dosage; the correlations for both male and female mice were essentially parallel (slope = 0.08 and 0.09, respectively). In addition, we found an effect of genomic imprinting on megakaryocyte DNA content in backcross offspring. The genetic imprinting was characterized by the female parent having a greater influence on the offspring's megakaryocyte DNA content than the male parent, ie, although the overall genetic makeup was the same, female offspring from backcross no. 6 (in which the female was C3H) had higher average megakaryocyte ploidy values than those from backcross no. 5 (in which the female was B6C3F1).(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMedDate not supplied

[Frequency of formation of mutants resistant to nystatin in polyploid strains of Candida scottii].

Polyploid strains of Candida scottii differ by their susceptibility to the action of nistatin. Haploid strain is most resistant, diploid strain is less resistant than haploid strain, and triploid strain is more susceptible than diploid strain. UV-treatment resulted in mutants which were 1.5--2 times more resistant to the action of nistatin than parent forms. The frequency of nistatin-resistant mutants increases with the ploidity of the cultures and with the doses of UV-irradiation.

Candida↗
PubMed1996

The role of p53 in the induction of polyploidity of myelomonocytic leukemic M1/2 cells.

p53 was shown to play a central role in the maintenance of genomic integrity. The present experiments suggest that p53 is involved in the control of cell ploidity. Using a p53 non-producer cell line, M1/2, that was reconstituted to express either wild type or mutant p53 protein, by infection with the temperature sensitive (Ts) p53Val135 virus, it was found that both loss of wild type p53 or overexpression of mutant p53, may be associated with the generation of cell polyploidity. Overexpression of mutant p53 protein enhanced the appearance of giant cells that further accumulated following gamma-irradiation. Expression of wild type p53 reduced the level of giant cells which accumulated in the parental M1/2 p53 non-producer cells following gamma-irradiation. This activity of the wild type p53 seems to be mediated by either the reduction in the rate of giant cell generation, as observed in M1/2 derived cell lines expressing low levels of wild type p53 protein or by facilitating their apoptosis, as observed in wild type p53 high-producer cells. The latter conclusion is further supported by the observation that isolated giant cells are directly induced to undergo apoptosis following wild type p53 expression.

Animals↗
PubMed2026

Ancient polyploidization waves as evolutionary shields for angiosperms.

Chen et al. identified 132 whole-genome duplications (WGDs) clustered around environmental crises. We highlight how, over longer evolutionary timescales, ancient WGDs convergently retained MADS-box, MYB, WRKY and HSF transcription factors, building stress-adaptation networks. These insights guide climate-resilient crop improvement through comparative genomics and CRISPR engineering.

MADS-box↗
PubMed1996

Increased stringency of the 1,25-dihydroxyvitamin D3-induced G1 to S phase block in polyploid HL60 cells.

Treatment of mammalian cells with 1,25-dihydroxyvitamin D3 (1,25D3) produces a G1 to S (G1/S) phase cell cycle block. In addition, it has been noted that a smaller proportion of cells accumulates in the G2/M compartment in 1,25D3-treated cultures. Since cyclins have a major influence on the regulation of cell cycle progression, we determined the expression of cyclins A and B as markers of the G2 phase and of cyclin E as the marker of G1/S transition. No increase in the steady-state levels of cyclin A or cyclin B mRNA was detected in the total cell population or in the cyclin B1 protein in the G2/M cell cycle compartment. In contrast, immunodetectable cyclin E protein was increased in cell cultures as a whole and specifically in the G2/M compartment cells. Determination of BrdU incorporation into DNA by flow cytometry showed marked inhibition of DNA replication in cells with DNA content higher than 4C, and autoradiography of 3H-TdR-pulsed cells showed that polynucleated cells did not replicate DNA after 96 h of treatment with 1,25D3 or analogs. Taken together, these experiments show that at least a portion of the G2/M compartment in 1,25D3-arrested cultures of HL60 cells represents G1 cells at a higher ploidy level, which are blocked from entering the high ploidy S phase.

Calcitriol↗
PubMed1988

MCA/MR syndrome in a female infant with tetraploidy mosaicism: review of the human polyploid phenotype.

We report on a 3-month-old girl with unusual facial appearance, short neck with low posterior hairline, wide chest, valvular pulmonic stenosis, abnormal fingernails, and diploid-tetraploid mosaicism (46,XX/92,XXXX in 7.2% of peripheral leucocytes and in 29% of skin fibroblasts). Comparison with 11 previously reported cases with mosaic or complete tetraploidy does not establish an easily recognizable syndrome. However, a malformation pattern is apparent when tetraploidy patients are compared with 14 cases of triploid mosaicism and 44 previously reported cases of nonmosaic triploidy. A history of sex hormone exposure was present in 5 of 11 pregnancies resulting in tetraploidy; this exposure may correlate with the occurrence of tetraploidy in polycystic ovary syndrome and in tumors of the female reproductive tract. The mechanism of dysmorphogenesis involved in polyploidy is considered, including hypotheses of altered nuclear/cytoplasmic ratio, of trophoblastic alteration, of delayed cell division, or of altered autosome/active X chromosome ratio.

Abnormalities, Multiple↗
PubMed2006

Mechanisms of genomic rearrangements and gene expression changes in plant polyploids.

Polyploidy is produced by multiplication of a single genome (autopolyploid) or combination of two or more divergent genomes (allopolyploid). The available data obtained from the study of synthetic (newly created or human-made) plant allopolyploids have documented dynamic and stochastic changes in genomic organization and gene expression, including sequence elimination, inter-chromosomal exchanges, cytosine methylation, gene repression, novel activation, genetic dominance, subfunctionalization and transposon activation. The underlying mechanisms for these alterations are poorly understood. To promote a better understanding of genomic and gene expression changes in polyploidy, we briefly review origins and forms of polyploidy and summarize what has been learned from genome-wide gene expression analyses in newly synthesized auto-and allopolyploids. We show transcriptome divergence between the progenitors and in the newly formed allopolyploids. We propose models for transcriptional regulation, chromatin modification and RNA-mediated pathways in establishing locus-specific expression of orthologous and homoeologous genes during allopolyploid formation and evolution.

Chromosomes, Plant↗
PubMed1977

Accumulation of polyploid cells and G2-phase cells during ascites tumor growth.

Ehrlich ascites tumor cells from the plateau phase of growth were transplanted into new hosts, pulse-labeled with tritiated thymidine and blocked with repeated injections of vinblastine. When unlabeled cells were analyzed for their cellular DNA content utilizing a cytophotometric technique it was found that in relation to the total number of cells (labeled plus unlabeled), 13% had a 2C DNA content, 36% a 4C DNA content and 5% and 8C DNA content at 0.5 hours after tranplantation. By 24 hours the distributions changed dramatically: the initally unlabeled 2C cells were now 4C, the 36% of the cells that were initially 4C partitioned into 24% that were still 4C and 12% that progressed to 8C, and the initial 8C cells remained 8C. These studies indicate that the accumulation of 4C cells during the plateau phase of growth is due to a combination of G2 diploid and G1 tetraploid cells.

Animals↗