scholarly journals Dicentric chromosome bridges in root tips and micronuclei in pollen tetrads induced by X rays and maleic hydrazide in Tradescantia clone BNL 4430.

1997 ◽  
Vol 72 (4) ◽  
pp. 187-195 ◽  
Author(s):  
Ling Zhi Xiao ◽  
Sadao Ichikawa
2019 ◽  
Vol 10 (1) ◽  
pp. 2 ◽  
Author(s):  
Yanti Lusiyanti ◽  
Mukh Syaifudin ◽  
Tuti Budiantari ◽  
Sofiati Purnami ◽  
Dwi Ramadhani

2009 ◽  
Vol 64 (3-4) ◽  
pp. 167-175 ◽  
Author(s):  
Ahmad Khalil ◽  
Ahmed Maslat ◽  
Abeer Hafiz ◽  
Shehadeh Mizyed ◽  
Muhammad Ashram

The ability of two calix[4]arene derivatives, namely 25,27-p-tert-butylcalix[4]dithiooxabenzocrown (1) and 25,27-p-tert-butylcalix[4]trithiooxabenzocrown (2), to produce chromosomal aberrations in root meristematic cells of Allium cepa and micronuclei (MN) in normochromatic erythrocytes (NCE) of Balb/c mice was investigated. NCE are normal mature red blood cells with a full complement of hemoglobin but lack ribosomes. In the first test, the root tips were treated with a series of concentrations of the two test chemicals ranging from 10 - 7 to 10 - 4 M for 24 or 48 h. Both compounds caused concentration-dependent increases in the percentage of aberrant cells and reductions in the mitotic index. These effects depended, to some extent, on the duration of the treatment. The most conspicuous chromosomal abnormalities were c-mitosis, chromosome bridges, chromosome breaks, chromosome lags as well as micronuclei and multinuclei. In the second test, acridine orange fluorescent staining was applied to evaluate the incidence of MN in NCE of mice intraperitoneally injected with varying contents of the two test chemicals (0.02 - 0.08 mg/mouse). The two chemicals induced dose-dependent MN formation as compared to the negative control. The second compound had more pronounced cytogenetic influence than the first one. Mitomycin C (MMC, 14 mg/kg body weight), employed as positive control, produced more obvious effects on the parameters investigated.


1961 ◽  
Vol 10 (4) ◽  
pp. 567-575 ◽  
Author(s):  
John J. Callaghan ◽  
Paul Grun

Allium cernuum, Vicia faba, and Tradescantia paludosa were treated by root immersion in maleic hydrazide (1 mM/liter) labeled with C14 (C14-MH) for 1 hour to determine the location within the cell to which MH moves during various periods of time after treatment. Root tips were fixed 24 hours, 48 hours, 72 hours, and 3 weeks after treatment. Autoradiographs of root tips squashed 24 to 72 hours after fixation showed that C14-MH was distributed throughout the nuclei and was particularly concentrated in the nucleoli. The nucleolar localization of the chemical was transitory, fixations made 3 weeks after treatment showing well labeled nuclei many of which completely lacked label in the nucleoli. The chromosomes seen in mitotic divisions of all three species had the same amount of label in euchromatic as heterochromatic areas. Since the chemical was not accumulated preferentially in heterochromatic areas, it seems likely that the reported specificity of MH for the breakage of heterochromatin can not be due to preferential heterochromatic incorporation.


1995 ◽  
Vol 344 (1-2) ◽  
pp. 5-12 ◽  
Author(s):  
Antonio De Marco ◽  
Claudio De Simone ◽  
Marcello Raglione ◽  
Paolo Lorenzoni

1958 ◽  
Vol 92 (867) ◽  
pp. 365-369 ◽  
Author(s):  
F. A. Haskins ◽  
Merwyn F. Davidson ◽  
Russell J. Beers

2020 ◽  
Vol 8 ◽  
Author(s):  
Ghazi A. Alsbeih ◽  
Khaled S. Al-Hadyan ◽  
Najla M. Al-Harbi ◽  
Sara S. Bin Judia ◽  
Belal A. Moftah

In cases of nuclear and radiological accidents, public health and emergency response need to assess the magnitude of radiation exposure regardless of whether they arise from disaster, negligence, or deliberate act. Here we report the establishment of a national reference dose–response calibration curve (DRCC) for dicentric chromosome (DC), prerequisite to assess radiation doses received in accidental exposures. Peripheral blood samples were collected from 10 volunteers (aged 20–40 years, median = 29 years) of both sexes (three females and seven males). Blood samples, cytogenetic preparation, and analysis followed the International Atomic Energy Agency EPR-Biodosimetry 2011 report. Irradiations were performed using 320 kVp X-rays. Metafer system was used for automated and assisted (elimination of false-positives and inclusion of true-positives) metaphases findings and DC scoring. DC yields were fit to a linear–quadratic model. Results of the assisted DRCC showed some variations among individuals that were not statistically significant (homogeneity test, P = 0.66). There was no effect of age or sex (P > 0.05). To obtain representative national DRCC, data of all volunteers were pooled together and analyzed. The fitted parameters of the radiation-induced DC curve were as follows: Y = 0.0020 (±0.0002) + 0.0369 (±0.0019) *D + 0.0689 (±0.0009) *D2. The high significance of the fitted coefficients (z-test, P < 0.0001), along with the close to 1.0 p-value of the Poisson-based goodness of fit (χ2 = 3.51, degrees of freedom = 7, P = 0.83), indicated excellent fitting with no trend toward lack of fit. The curve was in the middle range of DRCCs published in other populations. The automated DRCC over and under estimated DCs at low (<1 Gy) and high (>2 Gy) doses, respectively, with a significant lack of goodness of fit (P < 0.0001). In conclusion, we have established the reference DRCC for DCs induced by 320 kVp X-rays. There was no effect of age or sex in this cohort of 10 young adults. Although the calibration curve obtained by the automated (unsupervised) scoring misrepresented dicentric yields at low and high doses, it can potentially be useful for triage mode to segregate between false-positive and near 2-Gy exposures from seriously irradiated individuals who require hospitalization.


1930 ◽  
Vol s2-73 (292) ◽  
pp. 633-650
Author(s):  
RUTH E. P. PATTEN ◽  
SYLVIA B. WIGODER

1. The effect of X-rays is divisible into two periods, one showing the immediate effect, the second period being one of recovery. 2. The immediate effect includes gradual cessation of mitosis, and the production of abnormalities in those cells which were in the process of division or were about to divide at the time of irradiation. 3. The length of time during which no cells enter into mitosis depends on the size of the dose. 4. During the recovery period some cells again enter into mitosis but their division is usually of an abnormal type. 5. Irradiation acts on cells in the interphase by interfering with some physiological process. These cells are then unable to enter into mitosis until the effect of irradiation has passed off.


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