Repetitious Production of Similar Karyotypes in Different Plants of Haplopappus gracilis, an Annual Asteraceae, Following Exposure to Ionizing Radiation
Abstract:Following exposure to X-rays or reactor radiation at the early germinating stage, seedlings of Haplopappus gracilis (Nutt.) Gray were inspected for karyotypic changes in the meristems of lateral roots 2 months later. Among 210 plants studied in total, 12 were carriers of aberrant karyotypes in the root systems. One of them was a whole-body variant of spontaneous origin, showing a complete change of karyotype not only in the root system but also in the shoot system. The remainders were mosaics, showing a comple… Show more
“…1A). These findings are consistent with and confirm data in previous papers (Tanaka 1967, Yonezawa 1981a, Ikeda 1987, Hanmoto et al 2003. Fig.…”
Section: Standard Karyotype Of H Gracilissupporting
confidence: 94%
“…Out of 160 progenies, only one plant (designated as 78-465) possessed 2nϭ5 chromosomes. The other two plant materials, X18-38 and X18-49, were found growing among 133 plants from the achenes irradiated by X-rays just at the time of germination and had 2nϭ5 with a fragment-like chromosome (Hanmoto et al 2003).…”
Section: Plant Materialsmentioning
confidence: 99%
“…The preparation was the same as previously reported (Yonezawa 1981a, Hanmoto et al 2003: Root tips were pretreated with 0.002 M 8-hydroxyquinoline solution for 90 min at 18°C or 0.1% colchicine solution for 60 min at 20°C followed by fixation in 45% acetic acid solution for 15 min at 5°C. The tips were then macerated in a mixture of 1 N HCl and 45% acetic acid (2 : 1) for 15 s at 60°C.…”
Section: Chromosome Preparation and Karyotype Analysismentioning
confidence: 99%
“…We previously reported the karyotypes of 2nϭ5 observed in the plants irradiated by X-rays and pointed out that the extra centromere in the 2nϭ5 complement might be derived from the reactivation of the suppressed centromere in the chromosome 1 in H. gracilis (Hanmoto et al 2003).…”
Summary Rearranged karyotypes of 2nϭ5 present in three plants of Haplopappus gracilis (2nϭ4) were cytogenetically analyzed to clarify the origin of an additional centromere in the chromosome complement. One of the plants was a progeny of the homozygote with normal chromosome 1 crossed with the heterozygote with normal and centromere-shifted chromosome 1. The other two plants were derived from seedlings irradiated with X-rays during early germination stage. The chromosome complement of 2nϭ5 found in the first plant was comprised of 3 normal chromosomes (one chromosome 1 and two chromosome 2) and two rearranged chromosomes each possessing a centromere at the subterminal position. All the chromosome complements of the irradiated plants were similar to each other and each consisted of three normal chromosomes (one chromosome 1 and two chromosome 2) and 2 rearranged chromosomes, one large and metacentric and the other, fragmentlike. The origin of the additional centromere in each complement of 2nϭ5 is discussed from the point of chromosomal evolution in the genus Haplopappus.
“…1A). These findings are consistent with and confirm data in previous papers (Tanaka 1967, Yonezawa 1981a, Ikeda 1987, Hanmoto et al 2003. Fig.…”
Section: Standard Karyotype Of H Gracilissupporting
confidence: 94%
“…Out of 160 progenies, only one plant (designated as 78-465) possessed 2nϭ5 chromosomes. The other two plant materials, X18-38 and X18-49, were found growing among 133 plants from the achenes irradiated by X-rays just at the time of germination and had 2nϭ5 with a fragment-like chromosome (Hanmoto et al 2003).…”
Section: Plant Materialsmentioning
confidence: 99%
“…The preparation was the same as previously reported (Yonezawa 1981a, Hanmoto et al 2003: Root tips were pretreated with 0.002 M 8-hydroxyquinoline solution for 90 min at 18°C or 0.1% colchicine solution for 60 min at 20°C followed by fixation in 45% acetic acid solution for 15 min at 5°C. The tips were then macerated in a mixture of 1 N HCl and 45% acetic acid (2 : 1) for 15 s at 60°C.…”
Section: Chromosome Preparation and Karyotype Analysismentioning
confidence: 99%
“…We previously reported the karyotypes of 2nϭ5 observed in the plants irradiated by X-rays and pointed out that the extra centromere in the 2nϭ5 complement might be derived from the reactivation of the suppressed centromere in the chromosome 1 in H. gracilis (Hanmoto et al 2003).…”
Summary Rearranged karyotypes of 2nϭ5 present in three plants of Haplopappus gracilis (2nϭ4) were cytogenetically analyzed to clarify the origin of an additional centromere in the chromosome complement. One of the plants was a progeny of the homozygote with normal chromosome 1 crossed with the heterozygote with normal and centromere-shifted chromosome 1. The other two plants were derived from seedlings irradiated with X-rays during early germination stage. The chromosome complement of 2nϭ5 found in the first plant was comprised of 3 normal chromosomes (one chromosome 1 and two chromosome 2) and two rearranged chromosomes each possessing a centromere at the subterminal position. All the chromosome complements of the irradiated plants were similar to each other and each consisted of three normal chromosomes (one chromosome 1 and two chromosome 2) and 2 rearranged chromosomes, one large and metacentric and the other, fragmentlike. The origin of the additional centromere in each complement of 2nϭ5 is discussed from the point of chromosomal evolution in the genus Haplopappus.
“…Ames and Mitra (1968) and Hanmoto et al (2003) reported that the subdistal positions of the long arms in both 1g and 2g chromosomes of H. gracilis are the breakage points by maleic hydrazide treatment and by ionizing radiation, respectively. These points correspond well to the ITR sites revealed by FISH in the present study.…”
Section: Correlation Between Itrs Site and Chromosome Instabilitymentioning
Summary Fluorescence in situ hybridization (FISH) using an Arabidopsis-type telomeric sequence (TTTAGGG) n probe to the mitotic chromosomes of Haplopappus gracilis (nϭ2) revealed the presence of Interstitial Telomere-like Repeats (ITRs) in at the subdistal position of the long arm of both chromosome pairs (1g and 2g). The H. gracilis genome (nϭ2) is generally thought to reconstitute from the nϭ4 complement of the allied species, H. ravenii. The sites we identified by FISH are in close proximity to the chromosomal rearrangement fusion points. This evidence supports the hypothesis that the karyotype of H. garacilis evolved from that of H. ravenii due to chromosome breakage and the subsequent end-to-end chromosome fusion.
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